A JAK Inhibitor for Treatment of Rheumatoid Arthritis: The Baricitinib Experience

Baricitinib, an oral selective Janus kinase (JAK)1/JAK2 inhibitor, is approved as monotherapy or in combination with methotrexate for treating adults with moderate-to-severe active rheumatoid arthritis (RA) and provides improvements in clinical signs, symptoms and patient-reported outcomes. Currently, baricitinib is approved for treating RA in more than 75 countries. In several pivotal Phase II and III RA trials (RA-BALANCE, RA-BEGIN, RA-BEAM, RA-BUILD, RA-BEACON, RA-BEYOND), up to seven years of baricitinib treatment was well tolerated and provided rapid and sustained efficacy, which was confirmed in real-world settings. Safety signals for another JAK inhibitor, tofacitinib, have emerged, as observed in the post-marketing Phase IIIb/IV trial Oral Rheumatoid Arthritis Trial (ORAL) Surveillance; safety signals were subsequently highlighted in a retrospective study of baricitinib and consequently new recommendations and warnings and precautions for all JAK inhibitors have been issued. Ongoing studies to further characterise and clarify the benefit:risk of JAK inhibitors include registries and controlled trials. This capstone review summarises clinical and real-world data outlining the benefit:risk profile of baricitinib, confirming that the improved disease activity and physical function of patients with RA treated with this JAK inhibitor observed in clinical trials is translated into effectiveness in clinical practice, with a low rate of discontinuations.


Introduction
After two decades during which biologic disease-modifying antirheumatic drugs (bDMARDs) revolutionised the treatment and prognosis of patients with rheumatoid arthritis (RA), a new class of targeted synthetic DMARDS (tsDMARDs), Janus kinase inhibitors (JAKis), have been recognised by international societies as effective and welltolerated treatment options. While conventional synthetic DMARDs (csDMARDs) remain the recommended first-line 'anchor therapy' for patients with early RA [1,2], updated 2 of 29 European Alliance of Associations for Rheumatology (EULAR) management guidelines recommend adding a bDMARD or a JAKi to csDMARD therapy if symptoms are not sufficiently improved. JAKis should be considered only after risk assessment (see also Section 3.3. Safety below) but, in common with interleukin (IL)-6 inhibitors, may be favoured if combination therapy is contraindicated [2].
JAKis are small-molecule, targeted oral treatments with a rapid onset of action [3]. Baricitinib, an oral selective, and reversible, JAK1/JAK2 inhibitor was the first in the JAKi class to be approved to treat RA in the European Union (EU) [4] based on the demonstration of superior efficacy compared with placebo and tumour necrosis factor inhibitors (TNFis) in populations with an inadequate response (IR) to csDMARDs, including methotrexate (MTX) [5,6]. Baricitinib also demonstrated superior efficacy to MTX monotherapy in patients who had received no or minimal csDMARDs and who were naïve to bDMARDs [7] and was associated with clinical improvements in patients with an IR to bDMARDs [8].
Baricitinib's first global approval was in Japan, then the EU in 2017, as monotherapy or in combination with MTX for the treatment of adults with moderate-to-severe active RA who have responded inadequately to, or who are intolerant of one or more DMARDs [4,9]. Following this, approval was received in the United States (US) in 2018 for the treatment of adults with moderately to severely active RA who have had an IR to one or more TNFis [10]. Baricitinib is now licenced in more than 75 countries for the treatment of RA. In some markets, baricitinib is also approved as therapy for atopic dermatitis, COVID-19 and/or alopecia areata [9,10].
Five years after entering the market, evidence for baricitinib in long-term (up to seven years) extension studies of integrated data sets and real-world data are available and new data are emerging. Within this review, both clinical trial data and all current real-world data for baricitinib in the treatment of RA published to date are summarised and discussed.

Pharmacodynamic and Pharmacokinetic Properties of Baricitinib
In vitro, baricitinib inhibits JAK1 (half-maximal inhibitory concentration [IC 50 ] 5.9 nmol/L) and JAK2 (IC 50 5.7 nmol/L) but has lower potency against tyrosine kinase 2 (IC 50 53 nmol/L) and JAK3 (IC 50 560 nmol/L) [4]. In vitro analyses also showed that baricitinib inhibited JAK1/3 signalling to a lesser extent than upadacitinib and tofacitinib, with all three JAKis inhibiting the signalling of JAK2/2-dependent cytokines [11]. In the Phase III trial, RA-BUILD [5], patients demonstrated reductions in levels of biomarkers associated with synovial inflammation (C1M, C3M and C4M) and bone resorption (CTX-I), which together with clinical improvements and radiographic data suggests that baricitinib inhibits key pathological processes in RA [12]. A study assessing the effects of baricitinib and tofacitinib in mice also revealed that JAK inhibition increases bone mass, while the robust up-regulation of markers for osteoblast function-such as osteocalcin and Wnt signalling-were seen in osteoblasts exposed to JAKis in vitro; the anabolic effect of JAKis was illustrated by the stabilisation of β-catenin [13]. In people with RA, JAK inhibition induced bone-anabolic effects as evidenced by the repair of arthritic bone erosions after treatment with tofacitinib [13]. More recently, a prospective study reported for the first time that baricitinib treatment increases resistance to mechanical load, with estimated failure load and bone stiffness correlated with reduced cortical porosity, thereby improving the functional properties of bone [14].
The relatively short half-life of baricitinib (12.5 h [9]), and convenient once daily oral administration, brought a substantial change to the current treatment options for RA. Improvements in the American College of Rheumatology 20% (ACR20) response rate, the Disease Activity Score in 28 joints (DAS28) and other clinical outcomes were seen as early as the first week with baricitinib treatment as compared to MTX [7,9]. In humans, approximately 75% of the administered baricitinib dose is cleared in the urine and about 20% in the faeces; drug metabolism is mediated by CYP3A4, with <10% of the dose identified as undergoing biotransformation [9] (Table 1 [10,[15][16][17][18][19][20][21][22][23][24][25][26]). This has a direct clinical implication in patients with concomitant mild-to-moderate or moderate-to-severe renal impairment, who should receive a 2 mg dose in some circumstances [9]. As a result of moderate hepatic metabolism, baricitinib has limited potential for drug-drug interactions, with interactions evident only with probenecid (a strong organic anion transporter-3 [OAT3] inhibitor) [27]. This is in contrast to most other JAKis, which are associated with numerous drug-drug interactions (Table 1). Thus, in patients concomitantly receiving baricitinib and medications metabolised by the liver-such as ketoconazole, fluconazole or rifampicin-no dose adjustment is required. The synthetic nature of baricitinib eliminates the risk of immunogenicity (neutralising antibody response) and the temporary interruption of baricitinib does not cause a loss of response [28]. Importantly, when there is a need for drug discontinuation, 90% of the baricitinib dose is eliminated within 24 h [9]. Although baricitinib is contraindicated during pregnancy, in contrast to many other available therapies, it may be stopped as late as one week prior to a planned pregnancy [9]. the faeces; drug metabolism is mediated by CYP3A4, with <10% of the dose identified as undergoing biotransformation [9] (Table 1 [10,[15][16][17][18][19][20][21][22][23][24][25][26]). This has a direct clinical implication in patients with concomitant mild-to-moderate or moderate-to-severe renal impairment, who should receive a 2 mg dose in some circumstances [9]. As a result of moderate hepatic metabolism, baricitinib has limited potential for drug-drug interactions, with interactions evident only with probenecid (a strong organic anion transporter-3 [OAT3] inhibitor) [27]. This is in contrast to most other JAKis, which are associated with numerous drug-drug interactions (Table 1). Thus, in patients concomitantly receiving baricitinib and medications metabolised by the liver-such as ketoconazole, fluconazole or rifampicin-no dose adjustment is required. The synthetic nature of baricitinib eliminates the risk of immunogenicity (neutralising antibody response) and the temporary interruption of baricitinib does not cause a loss of response [28]. Importantly, when there is a need for drug discontinuation, 90% of the baricitinib dose is eliminated within 24 h [9]. Although baricitinib is contraindicated during pregnancy, in contrast to many other available therapies, it may be stopped as late as one week prior to a planned pregnancy [9].

Dose Flexibility
Baricitinib is available in two dosage strengths (2 mg and 4 mg), each administered once daily. Baricitinib 4 mg is the indicated starting dose, with potential to taper to 2 mg, in all countries except the US, Canada and China, where a dose of 2 mg is approved for treating RA. Patients aged ≥65 years and those with a history of chronic or recurrent infections should receive a dose of 2 mg according to EU recommendations [9]. Both baricitinib 4 mg and 2 mg are efficacious among different treatment populations [5,8,9,29].
Elderly patients often have comorbidities and require multiple concomitant medications, with concerns that treatments will be less effective, and the number of adverse events (AEs) increased [30]. Subgroup analysis of data from two Phase III trials in patients J. Clin. Med. 2023, 12, x FOR PEER REVIEW 3 of 29 the faeces; drug metabolism is mediated by CYP3A4, with <10% of the dose identified as undergoing biotransformation [9] (Table 1 [ 10,[15][16][17][18][19][20][21][22][23][24][25][26]). This has a direct clinical implication in patients with concomitant mild-to-moderate or moderate-to-severe renal impairment, who should receive a 2 mg dose in some circumstances [9]. As a result of moderate hepatic metabolism, baricitinib has limited potential for drug-drug interactions, with interactions evident only with probenecid (a strong organic anion transporter-3 [OAT3] inhibitor) [27]. This is in contrast to most other JAKis, which are associated with numerous drug-drug interactions (Table 1). Thus, in patients concomitantly receiving baricitinib and medications metabolised by the liver-such as ketoconazole, fluconazole or rifampicin-no dose adjustment is required. The synthetic nature of baricitinib eliminates the risk of immunogenicity (neutralising antibody response) and the temporary interruption of baricitinib does not cause a loss of response [28]. Importantly, when there is a need for drug discontinuation, 90% of the baricitinib dose is eliminated within 24 h [9]. Although baricitinib is contraindicated during pregnancy, in contrast to many other available therapies, it may be stopped as late as one week prior to a planned pregnancy [9].

Dose Flexibility
Baricitinib is available in two dosage strengths (2 mg and 4 mg), each administered once daily. Baricitinib 4 mg is the indicated starting dose, with potential to taper to 2 mg, in all countries except the US, Canada and China, where a dose of 2 mg is approved for treating RA. Patients aged ≥65 years and those with a history of chronic or recurrent infections should receive a dose of 2 mg according to EU recommendations [9]. Both baricitinib 4 mg and 2 mg are efficacious among different treatment populations [5,8,9,29].
Elderly patients often have comorbidities and require multiple concomitant medications, with concerns that treatments will be less effective, and the number of adverse events (AEs) increased [30]. Subgroup analysis of data from two Phase III trials in patients J. Clin. Med. 2023, 12, x FOR PEER REVIEW 3 of 29 the faeces; drug metabolism is mediated by CYP3A4, with <10% of the dose identified as undergoing biotransformation [9] (Table 1 [ 10,[15][16][17][18][19][20][21][22][23][24][25][26]). This has a direct clinical implication in patients with concomitant mild-to-moderate or moderate-to-severe renal impairment, who should receive a 2 mg dose in some circumstances [9]. As a result of moderate hepatic metabolism, baricitinib has limited potential for drug-drug interactions, with interactions evident only with probenecid (a strong organic anion transporter-3 [OAT3] inhibitor) [27]. This is in contrast to most other JAKis, which are associated with numerous drug-drug interactions (Table 1). Thus, in patients concomitantly receiving baricitinib and medications metabolised by the liver-such as ketoconazole, fluconazole or rifampicin-no dose adjustment is required. The synthetic nature of baricitinib eliminates the risk of immunogenicity (neutralising antibody response) and the temporary interruption of baricitinib does not cause a loss of response [28]. Importantly, when there is a need for drug discontinuation, 90% of the baricitinib dose is eliminated within 24 h [9]. Although baricitinib is contraindicated during pregnancy, in contrast to many other available therapies, it may be stopped as late as one week prior to a planned pregnancy [9].

Dose Flexibility
Baricitinib is available in two dosage strengths (2 mg and 4 mg), each administered once daily. Baricitinib 4 mg is the indicated starting dose, with potential to taper to 2 mg, in all countries except the US, Canada and China, where a dose of 2 mg is approved for treating RA. Patients aged ≥65 years and those with a history of chronic or recurrent infections should receive a dose of 2 mg according to EU recommendations [9]. Both baricitinib 4 mg and 2 mg are efficacious among different treatment populations [5,8,9,29].
Elderly patients often have comorbidities and require multiple concomitant medications, with concerns that treatments will be less effective, and the number of adverse events (AEs) increased [30]. Subgroup analysis of data from two Phase III trials in patients J. Clin. Med. 2023, 12, x FOR PEER REVIEW 3 of 29 the faeces; drug metabolism is mediated by CYP3A4, with <10% of the dose identified as undergoing biotransformation [9] (Table 1 [ 10,[15][16][17][18][19][20][21][22][23][24][25][26]). This has a direct clinical implication in patients with concomitant mild-to-moderate or moderate-to-severe renal impairment, who should receive a 2 mg dose in some circumstances [9]. As a result of moderate hepatic metabolism, baricitinib has limited potential for drug-drug interactions, with interactions evident only with probenecid (a strong organic anion transporter-3 [OAT3] inhibitor) [27]. This is in contrast to most other JAKis, which are associated with numerous drug-drug interactions (Table 1). Thus, in patients concomitantly receiving baricitinib and medications metabolised by the liver-such as ketoconazole, fluconazole or rifampicin-no dose adjustment is required. The synthetic nature of baricitinib eliminates the risk of immunogenicity (neutralising antibody response) and the temporary interruption of baricitinib does not cause a loss of response [28]. Importantly, when there is a need for drug discontinuation, 90% of the baricitinib dose is eliminated within 24 h [9]. Although baricitinib is contraindicated during pregnancy, in contrast to many other available therapies, it may be stopped as late as one week prior to a planned pregnancy [9].

Dose Flexibility
Baricitinib is available in two dosage strengths (2 mg and 4 mg), each administered once daily. Baricitinib 4 mg is the indicated starting dose, with potential to taper to 2 mg, in all countries except the US, Canada and China, where a dose of 2 mg is approved for treating RA. Patients aged ≥65 years and those with a history of chronic or recurrent infections should receive a dose of 2 mg according to EU recommendations [9]. Both baricitinib 4 mg and 2 mg are efficacious among different treatment populations [5,8,9,29].
Elderly patients often have comorbidities and require multiple concomitant medications, with concerns that treatments will be less effective, and the number of adverse events (AEs) increased [30]. Subgroup analysis of data from two Phase III trials in patients J. Clin. Med. 2023, 12, x FOR PEER REVIEW 3 of 29 the faeces; drug metabolism is mediated by CYP3A4, with <10% of the dose identified as undergoing biotransformation [9] (Table 1 [10,[15][16][17][18][19][20][21][22][23][24][25][26]). This has a direct clinical implication in patients with concomitant mild-to-moderate or moderate-to-severe renal impairment, who should receive a 2 mg dose in some circumstances [9]. As a result of moderate hepatic metabolism, baricitinib has limited potential for drug-drug interactions, with interactions evident only with probenecid (a strong organic anion transporter-3 [OAT3] inhibitor) [27]. This is in contrast to most other JAKis, which are associated with numerous drug-drug interactions (Table 1). Thus, in patients concomitantly receiving baricitinib and medications metabolised by the liver-such as ketoconazole, fluconazole or rifampicin-no dose adjustment is required. The synthetic nature of baricitinib eliminates the risk of immunogenicity (neutralising antibody response) and the temporary interruption of baricitinib does not cause a loss of response [28]. Importantly, when there is a need for drug discontinuation, 90% of the baricitinib dose is eliminated within 24 h [9]. Although baricitinib is contraindicated during pregnancy, in contrast to many other available therapies, it may be stopped as late as one week prior to a planned pregnancy [9].

Dose Flexibility
Baricitinib is available in two dosage strengths (2 mg and 4 mg), each administered once daily. Baricitinib 4 mg is the indicated starting dose, with potential to taper to 2 mg, in all countries except the US, Canada and China, where a dose of 2 mg is approved for treating RA. Patients aged ≥65 years and those with a history of chronic or recurrent infections should receive a dose of 2 mg according to EU recommendations [9]. Both baricitinib 4 mg and 2 mg are efficacious among different treatment populations [5,8,9,29].
Elderly patients often have comorbidities and require multiple concomitant medications, with concerns that treatments will be less effective, and the number of adverse events (AEs) increased [30]. Subgroup analysis of data from two Phase III trials in patients

Dose Flexibility
Baricitinib is available in two dosage strengths (2 mg and 4 mg), each administered once daily. Baricitinib 4 mg is the indicated starting dose, with potential to taper to 2 mg, in all countries except the US, Canada and China, where a dose of 2 mg is approved for treating RA. Patients aged ≥65 years and those with a history of chronic or recurrent infections should receive a dose of 2 mg according to EU recommendations [9]. Both baricitinib 4 mg and 2 mg are efficacious among different treatment populations [5,8,9,29].
Elderly patients often have comorbidities and require multiple concomitant medications, with concerns that treatments will be less effective, and the number of adverse events (AEs) increased [30]. Subgroup analysis of data from two Phase III trials in patients with RA and an IR to csDMARDs (csDMARD-IR)-RA-BUILD [5] and RA-BEAM [6]-demonstrated similar clinical efficacy with baricitinib 4 mg once daily in patients aged <50 years and those aged ≥65 years [30]. In general, while efficacy is not affected by age, safety might be diminished, with higher rates of discontinuation due to AEs in elderly patients aged ≥65 years, mainly related to an increased risk of serious infections [30]. A reduced dosage of baricitinib 2 mg/day is recommended in patients aged ≥65 years and those with moderate renal impairment, and may be appropriate for patients with a history of chronic or recurrent infections [9], and is also in line with the European Medicines Agency (EMA) Pharmacovigilance Risk Assessment Committee (PRAC) recommendation to use a lower effective dose for all JAKs across all indications when treating populations at risk of venous thromboembolism (VTE), cancer or major cardiovascular (CV) problems [31]. Therefore, based on extrapolation from the Oral Rheumatoid Arthritis Trial (ORAL) Surveillance [32] and the results of a retrospective analysis of baricitinib data [33], the lower dose of baricitinib 2 mg is recommended for all patients at risk of AEs of special interest (CV events, malignancy and deep vein thrombosis), with the possibility to step up to a higher baricitinib dose of 4 mg if disease activity is not controlled.

RA Populations
In Phase III RCTs conducted in countries across the world, baricitinib was evaluated in a range of patients with RA, including those who were bDMARD-naïve in RA-BEGIN [7], MTX-IR in RA-BEAM [6] and RA-BALANCE [34,35], csDMARD-IR in RA-BUILD [5] and bDMARD-IR (27% ≥3 prior bDMARDs) in RA-BEACON [8]. Baricitinib has been evaluated as monotherapy or in combination with MTX, with or without concomitant glucocorticoids.

Clinical Outcomes
In RA-BEGIN, baricitinib 4 mg/day, as monotherapy or in combination with MTX, had a rapid response with superior and improved efficacy outcomes (ACR20 at 24 weeks), clinically and functionally, when directly compared with MTX monotherapy in patients predominantly naïve to csDMARDs. Rates of remission (REM) and low disease activity (LDA) were also higher with both baricitinib regimens than with MTX [7].
In RA-BALANCE [34,35], RA-BUILD [5] and RA-BEAM [6], baricitinib was established as a treatment option for patients with an IR to one or more csDMARDs. In each trial, baricitinib showed significant rapid improvements in ACR20 response rates and other clinical outcomes relative to placebo [5,6,35], and for the first time, in RA-BEAM, versus adalimumab [6]. Specifically, in patients on background MTX, baricitinib 4 mg/day was the first JAKi to demonstrate clinical superiority by 12 weeks versus adalimumab with regard to the proportion of patients achieving ACR20 and DAS28-C-reactive protein (DAS28-CRP) change from baseline. In addition, patients treated with baricitinib demonstrated higher rates of REM (Simplified Disease Activity Index [SDAI] ≤3.3) as compared to adalimumab at 12 weeks [6].
In RA-BEACON, patients with an IR or intolerance to bDMARDs had significant functional and clinical improvements with baricitinib treatment, achieving greater benefits than those receiving placebo [8]. REM at 12 weeks, assessed by improvements in DAS28-CRP, was achieved at a significantly higher rate with baricitinib 2 mg/day and 4 mg/day than with placebo [8]. A post hoc analysis [36] reported that baricitinib was effective and superior to placebo, regardless of the previous number or type of concomitant bDMARDs, or glucocorticoid use.
In the long-term extension trial RA-BEYOND, baricitinib maintained efficacy and normative physical function for up to almost seven years in all three populations investigated (csDMARD-IR, including MTX-IR, and bDMARD-IR patients) ( Figure 1) [37,38]. Adapted from a pres tion by Caporali and colleagues [37]. a Data were also collected in RA-BEYOND from patients domised to placebo or adalimumab in the originating studies; the data shown here are from pat in the baricitinib treatment groups for the entire study duration. b Year three corresponds to weeks of the originating study RA-BUILD and 160 weeks of the originating study RA-BEAM. c seven corresponds to 360 weeks of the originating study RA-BUILD and 364 weeks of the origin study RA-BEAM. d Entry to RA-BEYOND was at 24 weeks of the originating study RA-BUILD 52 weeks of the originating study RA-BEAM. e Patients were analysed by treatment assigned at domisation in the originating study, regardless of rescue. CDAI, Clinical Disease Activity In LDA, low disease activity; W, week.
There are currently no head-to-head trials comparing the efficacy of the JAKis. H ever, in non-inferiority studies, only baricitinib 4 mg [6] and upadacitinib 15 mg [39] h shown superiority to adalimumab in prespecified endpoints, whereas tofacitinib [40] filgotinib have not [41].

Radiographic Outcomes
Before the era of bDMARDs, radiographic progression was the main reason for ability and early retirement in difficult-to-treat (D2T) patients with RA. With new tr ment options and a treat-to-target approach focused on the reduction of inflamma rapid achievement of REM or LDA is accompanied by no or limited structural joint d age [1,2].
In csDMARD-naïve patients (RA-BEGIN), radiographic progression seen with b citinib plus MTX was significantly less than that seen with MTX monotherapy both a and 52 weeks [7]. Post hoc analysis showed that patients achieving sustained clinica sponse (DAS28-high-sensitivity CRP ≤3.2 or SDAI score ≤11) at 52 weeks were less li to experience structural damage progression and that patients achieving these respo were less likely to progress if in the baricitinib or the baricitinib plus MTX group c pared to the MTX monotherapy group [42]. In MTX-IR patients (RA-BEAM), the inh tion of radiographic progression (modified total Sharp score [mTSS]) was significa greater with baricitinib than with placebo at 24 weeks [6]. Progression of bone erosion joint space narrowing were each similarly inhibited by baricitinib and adalimumab. In estingly, in a post hoc analysis of RA-BEGIN and RA-BEAM, reduced structural prog  [37]. a Data were also collected in RA-BEYOND from patients randomised to placebo or adalimumab in the originating studies; the data shown here are from patients in the baricitinib treatment groups for the entire study duration. b Year three corresponds to 156 weeks of the originating study RA-BUILD and 160 weeks of the originating study RA-BEAM. c Year seven corresponds to 360 weeks of the originating study RA-BUILD and 364 weeks of the originating study RA-BEAM. d Entry to RA-BEYOND was at 24 weeks of the originating study RA-BUILD and 52 weeks of the originating study RA-BEAM. e Patients were analysed by treatment assigned at randomisation in the originating study, regardless of rescue. CDAI, Clinical Disease Activity Index; LDA, low disease activity; W, week.
There are currently no head-to-head trials comparing the efficacy of the JAKis. However, in non-inferiority studies, only baricitinib 4 mg [6] and upadacitinib 15 mg [39] have shown superiority to adalimumab in prespecified endpoints, whereas tofacitinib [40] and filgotinib have not [41].

Radiographic Outcomes
Before the era of bDMARDs, radiographic progression was the main reason for disability and early retirement in difficult-to-treat (D2T) patients with RA. With new treatment options and a treat-to-target approach focused on the reduction of inflammation, rapid achievement of REM or LDA is accompanied by no or limited structural joint damage [1,2].
In csDMARD-naïve patients (RA-BEGIN), radiographic progression seen with baricitinib plus MTX was significantly less than that seen with MTX monotherapy both at 24 and 52 weeks [7]. Post hoc analysis showed that patients achieving sustained clinical response (DAS28-high-sensitivity CRP ≤3.2 or SDAI score ≤11) at 52 weeks were less likely to experience structural damage progression and that patients achieving these responses were less likely to progress if in the baricitinib or the baricitinib plus MTX group compared to the MTX monotherapy group [42]. In MTX-IR patients (RA-BEAM), the inhibition of radiographic progression (modified total Sharp score [mTSS]) was significantly greater with baricitinib than with placebo at 24 weeks [6]. Progression of bone erosion and joint space narrowing were each similarly inhibited by baricitinib and adalimumab. Interestingly, in a post hoc analysis of RA-BEGIN and RA-BEAM, reduced structural progression (mTSS) was observed regardless of disease activity control (Clinical Disease Activity Index [CDAI] REM and LDA versus CDAI moderate and high disease activity) in baricitinib-treated patients, but not in those who received placebo or MTX [43], providing evidence of an uncoupling of the link between disease activity and radiographic progression previously demonstrated with TNFis, IL-6 inhibitors and rituximab [44][45][46].

Patient-Reported Outcomes: Pain and Physical Function
Typically, clinicians focus on composite disease activity scores to assess disease control with a view to preventing structural progression and optimising function in RA. However, for many patients with RA, pain and fatigue are dominant symptoms [48,49]. Pain and impairment of other subjective quality of life measures may persist even after clinical targets for disease activity are achieved [50][51][52].
Patients treated with baricitinib (monotherapy or in combination with MTX) demonstrated more rapid and greater pain relief relative to placebo, MTX monotherapy and adalimumab in RCTs [5,6,36,53]. Relative to MTX monotherapy, baricitinib provided improvements in pain, health-related quality of life, Patient's Global Assessment of Disease Activity, fatigue and work and activity impairments in RA-BEGIN [54]. Additionally, patients treated with baricitinib in RA-BEAM demonstrated greater improvements in physical function than adalimumab, with more patients achieving Health Assessment Questionnaire-Disability Index (HAQ-DI) score improvement ≥0.22 or ≥0.3 at 24 weeks, an improvement considered as the minimally clinically important difference [6]. Furthermore, baricitinib-treated patients in RA-BEAM experienced a significant reduction in pain as compared to those treated with adalimumab as early as 2 weeks and tiredness as early as 8 weeks [6], which was associated with improved daily activity and work productivity by 12 and 24 weeks [55]. Post hoc analysis of RA-BEAM demonstrated that the median time needed for an improvement in pain of ≥50% was 4 weeks for baricitinib and 7.9 weeks with adalimumab [56]. In patients with uncontrolled inflammation after 24 weeks, as measured by a CRP level >10 mg/L, mean improvement in pain with baricitinib was significantly larger than with either adalimumab or placebo, with the study authors suggesting an effect of baricitinib on pain irrespective of inflammation control [56]. In exploratory analyses of these data, patients in LDA or REM (DAS28-erythrocyte sedimentation rate [DAS28-ESR]) had improvements in pain and HAQ-DI scores with baricitinib that were significantly larger than those seen with both placebo and adalimumab [57]. This finding led the authors to suggest that, in patients with well-controlled RA, baricitinib may exhibit effects beyond immunomodulation [57]. In a matching-adjusted indirect comparative analysis, the efficacy of several DMARDs on pain and HAQ-DI was assessed [54]. With the three matching methods used, baricitinib monotherapy consistently showed greater reductions in pain and improved physical function than tocilizumab and adalimumab monotherapy [54]. Statistically significant differences between baricitinib and tofacitinib treatment in pain reduction and improved physical function were not consistently observed [54]. Significantly greater improvements in most patient-reported outcomes (Short Form-36 Physical Component Summary, EQ-5D 5L components, Functional Assessment of Chronic Illness Therapy-Fatigue, Patient Global Assessment [PGA] and visual analogue scale [VAS] scores for pain) were experienced at 24 weeks with baricitinib 2 mg/day and 4 mg/day versus placebo in bDMARD-IR patients (RA-BEACON [58]).
As structural damage, reduced functionality and associated pain and reduction in quality of life can begin early in the disease course, the superiority of baricitinib to TNFi therapy may be of interest to healthcare providers and patients.

Temporary Treatment Interruption and Tapering
Temporary interruption to RA therapy is a common occurrence in clinical trials due to factors such as non-compliance, the necessity for surgery or AEs [28]. Analysis of the Phase III baricitinib studies RA-BEAM, RA-BUILD and RA-BEACON showed that 8.5-18.1% of patients interrupted their treatment through 24 weeks and that the most common cause of baricitinib treatment interruption was AEs (79.2-91.9% of interruptions), with treatment interruption lasting less than 2 weeks and generally occurring within the first two months of baricitinib treatment. In MTX-naïve patients, the first interruption occurred on average at 4-5 months [28]. During the brief baricitinib interruptions, RA symptoms increased in many patients (>59% for morning joint stiffness [MJS] duration and 86-90% for MJS severity, worst tiredness and worst joint pain), albeit minimally (increase of ≤30 min for MJS duration, increase of ≤2 units for other outcomes), and after the resumption of baricitinib treatment, symptoms resolved. Although AEs were the most frequent reason for baricitinib treatment interruption, these events infrequently reoccurred once treatment was restarted [28]. This indicates that AEs were usually short-term and are unlikely to impede efficacy, consistent with long-term efficacy outcomes that were not impacted by treatment interruptions [28].
Guidelines from the American College of Rheumatology (ACR) [1] and the EULAR [2] recommend that tapering DMARD therapy may be considered in patients who achieve sustained REM. Results from the long-term study RA-BEYOND demonstrated that patients with sustained LDA or REM on baricitinib 4 mg/day for ≥15 months, who then continued on baricitinib 4 mg/day or tapered to 2 mg/day, maintained LDA (80% 4 mg; 67% 2 mg) and REM (40% 4 mg; 33% 2 mg) at 48 weeks [59]. Dose reduction resulted in small, yet statistically significant increases in disease activity at 12, 24 and 48 weeks and produced earlier and more frequent relapse (loss of step-down criteria) over 48 weeks compared with 4 mg maintenance (23% 4 mg vs. 37% 2 mg, p = 0.001). At the same time, patients tapered to baricitinib 2 mg/day had numerically fewer infections, including non-serious infections, than those who continued on baricitinib 4 mg/day [59]. Overall, RA-BEYOND showed that baricitinib 2 mg/day provided acceptable efficacy, with only one in five patients returned to the 4 mg/day dose, which then resulted in disease control similar to that prior to tapering in the vast majority [59]. This may be of particular interest for managing the treatment of patients with safety concerns.

Characteristics of Baricitinib-Treated Patients in Real-World Settings
Real-world evidence (RWE) helps health authorities and healthcare providers (HCPs) gain further insights regarding treatment effectiveness and safety in real-life settings as they focus on heterogenous patient populations (who can be older, more treatment refractory, with more comorbid conditions and with more co-treatments than clinical trial populations). RWE permits the identification of associations between treatment and rare AEs and informs whether a drug's performance as assessed in RCTs is recapitulated in real-life settings. It also helps the medical community to better understand treatment patterns, such as line of therapy utilisation, or to define risks associated with lower effectiveness or poorer drug survival. Furthermore, RWE helps HCPs understand whether drug utilisation reflects official guidelines such as those of EULAR [2] and ACR [1]. Finally, RWE allows for longer drug exposure observations and comparisons with greater numbers of other drugs than RCTs typically provide. Below is a comprehensive descriptive review of the literature regarding RWE for baricitinib that has been reported to date; data were sourced from registries, monocentric and multicentric clinical practice studies, administrative or insurance claim databases, or prospective observational studies. At the time of writing, 41 published sources for RWE of baricitinib in the treatment of RA were identified [29,33,.
Due to the heterogeneity between each data source-such as patient characteristics and outcomes reported-a meta-analysis was not feasible.
Supplementary Table S1 summarises available baseline characteristics of baricitinibtreated patients in real-world settings [29,33,. The typical patient in the various RWE sources is aged about 60 years (which is older than the mean age of patients in baricitinib RCTs). In the RWE sources, only a limited number of patients were bio-naïve and most tended to have several b/tsDMARD failures before initiating baricitinib. In an observational Italian prospective study (IPS), patients treated with baricitinib who were bDMARD-naïve were younger with shorter disease duration and presented with fewer comorbidities, including CV disease, hypercholesterolaemia and diabetes, than those who were bDMARD-IR [64]. A study from the British Society for Rheumatology Biologics Register for Rheumatoid Arthritis (BSRBR-RA) also showed that bDMARDnaïve patients treated with baricitinib had shorter disease duration and numerically fewer comorbidities compared with the bDMARD-IR patients [29]. The proportion of patients treated with baricitinib monotherapy varies significantly between countries; for example, the proportion was 43% in Spain (ORBIT-RA registry) [60] and 87% in Denmark (DANBIO registry) [66] but is overall around 50%. With regard to dosage, most patients were using 4 mg (see Supplementary Table S1) and one study in bionaïve patients included in a Spanish registry (BIO-1) reported that patients who received baricitinib 2 mg were older than those who received baricitinib 4 mg (73 years vs. 56 years, p < 0.0001) [61]. An older age of patients treated with baricitinib 2 mg versus 4 mg (67.9 years vs. 61.7 years) was also identified in a Japanese post-marketing surveillance (PMS) study in which >70% of patients had an IR to at least one prior b/tsDMARD [76], as well as in the BSRBR-RA (67.6 years vs. 58.7 years) [29]. This reflects that rheumatologists are cautious and apply label recommendations for a lower baricitinib dosage when treating elderly patients.

Treatment Outcomes for Baricitinib in Real-Life Settings
Despite baricitinib use in patients predominantly refractory to previous cs/b/tsDMARD treatment, baricitinib demonstrated effectiveness in the majority of patients, as reflected by DAS28-ESR, DAS28-CRP and CDAI LDA and REM rates after six months of treatment ( Figure 2). Significant improvements were reported in two Italian monocentric studies, which used clinical and ultrasound evaluation (at Careggi University Hospital in Florence and at Sapienza University of Rome in Rome) as early as at one month for joint scores and other clinometric scores [78,83], as well as in a Japanese registry, Tsurumai Biologics Communication Registry of RA patients (TBCR-RA), for DAS28-CRP change from baseline [74]. In one of the monocentric studies from Italy, the clinical response to baricitinib was not affected by previous bDMARD exposure [78]. Five observational studies-two prospective multicentric studies from Italy, the IPS [64] and an analysis at Sapienza University of Rome [78]; a prospective, monocentric real-world analysis in Erlangen, Germany [82]; a Lilly-conducted multicentre prospective study [77]; and a study based on data from a Spanish registry, ORBIT-RA [60]-all confirmed that baricitinib alleviates pain, while the Lilly-conducted study and a study using data from the Swedish Rheumatology Quality (SRQ) register by the Anti-Rheumatic Therapy in Sweden (ARTIS) Study Group reported that baricitinib improves physical function, as highlighted by improvements in HAQ-DI scores [65,77].

Factors Affecting Treatment Outcomes-Drug Discontinuation, Drug Survival a Effectiveness
Understanding the risk factors associated with early discontinuation of drug tr ment, should it be for poor tolerance, lack of efficacy or other reasons, allows us to ta step closer to personalised medicine. Several studies discussed below investigated fac associated with a higher risk of JAKi treatment discontinuation; most studies investiga baricitinib [60,62,74,82,85] and two considered baricitinib and tofacitinib [71,84].
Patients stratified by age (<65 years and ≥65 years) presented similar rates of b citinib drug survival in ORBIT-RA [60], indicating no clear association between age drug survival, whereas increased age was associated with higher drug survival in a based (Southampton) study [85]. In the BSRBR-RA, during the first six months of tr ment, there seemed to be minimal difference in drug survival between patients aged low or above 65 years but over time, older patients tended to discontinue the drug m frequently [29]. A single centre study by Deprez and colleagues [84] found that increa age, glucocorticoid usage at baseline and number of comorbidities were associated w an increased risk of JAKi discontinuation. The ORBIT-RA registry supports that a gre number of comorbidities is associated with a higher risk of baricitinib discontinuation and a study of patients with RA in the Swiss Clinical Quality Management in Rheum Diseases Foundation (SCQM) register also identified that concomitant glucocorticoid

Factors Affecting Treatment Outcomes-Drug Discontinuation, Drug Survival and Effectiveness
Understanding the risk factors associated with early discontinuation of drug treatment, should it be for poor tolerance, lack of efficacy or other reasons, allows us to take a step closer to personalised medicine. Several studies discussed below investigated factors associated with a higher risk of JAKi treatment discontinuation; most studies investigated baricitinib [60,62,74,82,85] and two considered baricitinib and tofacitinib [71,84].
Patients stratified by age (<65 years and ≥65 years) presented similar rates of baricitinib drug survival in ORBIT-RA [60], indicating no clear association between age and drug survival, whereas increased age was associated with higher drug survival in a UK-based (Southampton) study [85]. In the BSRBR-RA, during the first six months of treatment, there seemed to be minimal difference in drug survival between patients aged below or above 65 years but over time, older patients tended to discontinue the drug more frequently [29]. A single centre study by Deprez and colleagues [84] found that increased age, glucocorticoid usage at baseline and number of comorbidities were associated with an increased risk of JAKi discontinuation. The ORBIT-RA registry supports that a greater number of comorbidities is associated with a higher risk of baricitinib discontinuation [60] and a study of patients with RA in the Swiss Clinical Quality Management in Rheumatic Diseases Foundation (SCQM) register also identified that concomitant glucocorticoid use at baseline, as well as higher disease activity, is associated with a higher risk of JAKi treatment discontinu-ation [62]. In line with this, the Japanese TBCR-RA [74] showed that higher disease activity (measured by DAS28-CRP) was independently associated with lack of achievement of LDA (EULAR response criteria) with baricitinib. In the German Erlangen cohort, prior bDMARD use appeared to be associated with lower baricitinib continuation [82], a finding also seen in the BSRBR-RA [29], while a trend for an increased number of bDMARDs and lower continuation was observed in the ORBIT-RA study [60]. In the aforementioned Japanese registry, no previous b/tsDMARD use was independently associated with the achievement of EULAR LDA [74]. However, although high baseline HAQ-DI and a high number of prior bDMARDs were associated with JAKi (tofacitinib and baricitinib) discontinuation and resistance to JAKi treatment (the patient did not achieve LDA [CDAI score ≤2.8] after 24 weeks), these associations were not demonstrated for baricitinib alone in multivariate logistic regression analyses in the Japanese FIRST registry (pharmaco-resistance hazard ratio [HR] of 1.41; p = 0.09 [71]). In the IPS, the authors reported that bDMARD-naïve patients had greater improvements in CDAI scores compared with those who had an IR to bDMARDs, and as a potential consequence, a higher treatment discontinuation rate in the bDMARD-IR population was observed [64]. Most of these observations from RWE contrast with baricitinib RCT data that showed no impact of prior biologic usage on baricitinib efficacy [36]. Monotherapy showed similar drug survival as compared to combination therapy in SCQM-RA [63] and this was confirmed in the BSRBR-RA up to six months [29]; however, at 12 months follow-up in the BSRBR-RA, it seemed monotherapy was associated with higher drug survival, but this was not statistically tested [29]. By contrast, a retrospective, longitudinal cohort study of patient data from the Spanish ORBIT-RA registry showed that baricitinib drug survival was higher with combination therapy, although again no formal statistical analysis was performed [60].
In summary, high disease activity, concomitant glucocorticoids, increased number of previous b/tsDMARDs and greater number of comorbidities are generally associated with baricitinib treatment discontinuation. However, no consistent trends were observed with regard to an effect of age and concomitant csDMARDs on treatment discontinuation.

Effectiveness of Baricitinib Monotherapy in RWE Settings
In the Swedish ARTIS study, baricitinib was as effective when used in monotherapy as in combination with a csDMARD, as highlighted by a good EULAR DAS28-ESR response, HAQ-DI improvement (defined as a decrease in HAQ-DI >0.2 at one-year evaluation compared with baseline) and CDAI REM (CDAI ≤2.8 at one-year evaluation) [65]. Monocentric studies in Erlangen, Germany, and Sapienza University of Rome, Italy, also found that baricitinib effectiveness was similar between monotherapy and combination therapy [78,82]. Additionally, a multicentre Italian study showed that compared with baricitinib monotherapy, the use of concomitant MTX was not associated with differences in REM (DAS28-CRP <2.6 and CDAI ≤2.8) and LDA (DAS28 ≥2.6 and ≤3.2 and CDAI ≤10) rates in both bDMARD-naïve and -IR patients [64]. These results of no differences in effectiveness between baricitinib monotherapy and combination therapy are consistent with those of two Japanese RWE studies, one that used DAS28-CRP data from the multicentre TBCR-RA [74] and a prospective, observational, multicentre study that used DAS28-ESR outcomes [75]. Finally, studies utilising Italian claims databases showed that csDMARDs could be tapered/discontinued in some baricitinib-treated patients [87,88]. In the analysis of data from patients with a diagnosis of RA during 2018, 69.8% of patients were using concomitant csDMARDs at baseline, which was reduced to 34.2% at follow-up, an effect most frequently observed in bDMARD-naïve patients [87]. In the analysis of data from patients with a diagnosis of RA during 2019, concomitant csDMARD use was 73.9% at baseline and 41.1% at follow-up; again, the reduction in csDMARD use was most pronounced in bDMARD-naïve patients [88].

Effect of Baricitinib on Glucocorticoid Tapering
Italian studies and the multinational, prospective observational study, RA-BE-REAL, demonstrated that baricitinib allows a reduction of glucocorticoid use [64,77,78], which is in line with the latest EULAR recommendations [2]. Patients who are pharmaco-resistant are usually taking more glucocorticoids [99], and baricitinib allowed tapering of glucocorticoids in both bDMARD-naïve and bDMARD-IR patients. In an Italian administrative claims database, 87.9% of 149 baricitinib-treated patients were using concomitant glucocorticoids at baseline, a number that was almost halved at the follow-up visit when 45.7% of patients were still using glucocorticoids [87]. This finding was confirmed in a later analysis by the same authors in 445 baricitinib-treated patients [88]. Furthermore, two cohort studies (Italian and Japanese) also reported a reduction in glucocorticoid utilisation [74,83]. The Italian monocentre study at Careggi University Hospital in Florence, Italy showed that prednisone-equivalent was used at a mean daily dosage of 6.25 mg at baseline (with 74.4% of patients using glucocorticoids), which decreased from baseline to 2.75 mg after three months and to 1.86 mg after six months of treatment (p < 0.0001 for both) (with 40% patients remaining on glucocorticoids) [83]. The Japanese study from the TBCR-RA, showed that the dosage of prednisolone used (3.9 mg/week) decreased from baseline, when baricitinib was initiated, to 24 weeks (3.2 mg/week; p = 0.006) [74].

Effect of Baricitinib on Ultrasound-Assessed Inflammation
Not only are clinical scores improved with baricitinib, but there is evidence to confirm that inflammatory processes are decreased in baricitinib-treated patients. Two Italian monocentric studies investigated the effect of baricitinib treatment on inflammation, as measured by ultrasound [78,83]. Tesei and colleagues (2021) [83] reported that synovitis and tenosynovitis analysed with greyscale or with power Doppler were significantly improved as early as at one month of treatment, while erosion scores remained unchanged throughout the six-month duration of the study, whereas Spinelli and colleagues (2021) [78] reported reductions in US inflammatory scores, reflecting the joint inflammatory status, as early as at one month of treatment. These observations were confirmed in another monocentric study, in Daegu, Republic of Korea [86], and are in line with the observed decrease in inflammatory biomarkers associated with joint destruction in RCTs of baricitinib [12].

RWE Effectiveness and Drug Survival of Baricitinib Compared to TNFi and Other Mode of Action bDMARDs
Five real-world studies allowed comparison of the effectiveness of baricitinib versus TNFi treatment, four were register-based studies-SCQM-RA [62], ARTIS [65], DAN-BIO [66] and BIO-1 [61]-and one was a prospective observational study-RA-BE-REAL [77], that compared baricitinib with b/tsDMARDs (other than baricitinib). Table 2 shows that baricitinib-treated patients were generally older, with a longer disease duration and more previous treatments (statistical testing was not consistently reported). This suggests that despite EULAR recommendations to either use a TNFi or, after risk assessment, a JAKi in patients with an IR to csDMARD treatment [2], current practice is still to favour a TNFi as first line, and then baricitinib as second line or later in the treatment algorithm. With regard to effectiveness (see Table 3), CDAI LDA and REM rates at one year were similar between patients in the SCQM-RA treated with baricitinib and TNFis [62], whereas the ARTIS study reported greater improvements in CDAI and HAQ-DI after three months and one year in baricitinib-versus TNFi-treated patients [65]. Six-month interim analysis of data from RA-BE-REAL also suggested that a higher proportion of patients reached CDAI remission with baricitinib compared with b/tsDMARDs (25.6% vs. 18.5%) but no formal statistical testing was performed [77]. In these three studies and two other studies (Table 3), drug survival was consistently higher with baricitinib, especially after adjusting for confounding variables, which is critical when looking at unbalanced cohorts. Adjusted drug survival was higher for baricitinib versus TNFis in the Spanish BIO-1 registry in which all patients were bio-naïve [61].  Several other studies have investigated the effectiveness and drug survival of baricitinib versus bDMARDs and other tsDMARDs. In the FIRST registry in Japan, CDAI scores were lower for baricitinib versus tofacitinib after 24 weeks, at which time significantly higher rates of CDAI LDA and REM were observed in the baricitinib cohort. In this study, the risk of selection bias was reduced by use of the propensity score-based inverse probability treatment weighted method [71]. In the study from the ARTIS Study Group, baricitinib effectiveness, measured using DAS28-ESR, HAQ-DI and CDAI at three months and one year, was compared to that of abatacept, IL-6 inhibitors, rituximab and tofacitinib, and almost all comparisons showed at least similar, if not numerically or significantly higher, rates of effectiveness with baricitinib versus the other mode of action DMARDs; the exception was DAS28-ESR, which showed significantly better improvement and more 'good' EULAR responders with IL-6 inhibitors versus baricitinib at three months and one year, respectively [65]. Notably, the study from the ARTIS Study Group also reported that baricitinib as monotherapy was more effective for HAQ-DI improvement than abatacept, IL-6 inhibitors, rituximab, TNFis and tofacitinib used as monotherapy. Similar trends were also observed for CDAI REM rates, but differences were not significant, with the exception of the comparison with rituximab [65]. In the TBCR-RA, propensity score matched patients receiving baricitinib or tocilizumab generally had similar improvements in tender and swollen joint count and serum CRP levels, but PGA of disease activity was significantly more improved with baricitinib [73]. In addition, a significantly higher proportion of patients receiving baricitinib achieved Boolean REM at 24 weeks as compared to tocilizumab (33% vs. 15%, p = 0.027) [73]. These real-world findings support those of a matching-adjusted indirect comparison showing better efficacy of baricitinib versus tocilizumab in HAQ-DI score and VAS pain using data from RCTs [54]. Interestingly, when stratifying patients based on CRP decreases after 24 weeks of treatment, baricitinib, but not tocilizumab, was associated with improved PGA in patients who did not achieve target reductions in CRP levels [73]. Since pain is a dominant factor driving PGA [48,100], this observation appears to support the RCT analysis from Taylor and colleagues (2019) that reported an effect of baricitinib on pain irrespective of inflammation [56]. In the Kansai Consortium for Well-being of Rheumatic Disease Patients (ANSWER) registry of patients with RA in Japan, no difference was observed with regard to treatment discontinuation rates at 18 months between baricitinib, tofacitinib and sarilumab [70]. The lack of difference in drug survival between baricitinib and tofacitinib was also demonstrated in 24-week analyses from the FIRST registry in Japan [71]. However, the HRs for discontinuation for baricitinib were significantly lower compared with those for tofacitinib, IL-6 inhibitors and abatacept, but higher than those for rituximab, after adjusting for confounding variables in the SRQ registry in the study from the ARTIS Study Group [65]. In adjusted analyses, treatment discontinuation was significantly less likely with baricitinib than with adalimumab, tofacitinib, abatacept, certolizumab pegol, golimumab, sarilumab and infliximab in the study from the Danish DANBIO registry, and the numerical lower risk of discontinuation versus etanercept and tocilizumab did not reach significance; rituximab had a lower risk of discontinuation than baricitinib, but this difference was not significant [66].
Treatment of D2T RA is a great unmet need for clinicians. Analysis of data from 353 patients with D2T RA in the FIRST registry in Japan showed that JAKis significantly improved CDAI compared to TNFis after adjustment using the propensity-based inverse probability treatment weighted method whereas for IL-6 inhibitors and abatacept, CDAI improvement was not significantly different from that of TNFi. The HRs of severe AEs were comparable among the four treatment subgroups, JAKis, TNFis, IL-6 inhibitors and abatacept, in both D2T and b/tsDMARD-naïve patients [101].

To Cycle or to Switch?
It is important to initiate a treatment change when RA is not sufficiently controlled since uncontrolled disease activity leads to an increased risk of comorbidities, including major adverse CV events (MACE) [102], VTE [103], malignancies [104] and serious infection [105]. EULAR recommendations for a treatment change allow for either cycling within a drug class or switching the mode of action of b/tsDMARDs [2]. After a TNFi-IR, both strategies have been shown to be valid [7,[106][107][108][109]. However, an RCT showed that after a primary TNFi-IR, switching to a DMARD with another mode of action led to a higher percentage of patients attaining LDA at 24 weeks and one year as compared with patients who cycled to another TNFi (45% vs. 28% at 24 weeks; odds ratio [OR], 2.09; 95% confidence interval [CI], 1.27 to 3.43; p = 0.004 and 41% vs. 23% at 52 weeks; OR, 2.26; 95% CI, 1.33 to 3.86; p = 0.003) [110]. Another meta-analysis that included RCTs and observational studies confirmed that switching to a different mode of action DMARD after a TNFi failure is more effective and also associated with lower rates of withdrawal than cycling to a different TNFi [111]. Finally, patients from RA-BEAM initiated on treatment with adalimumab who were either rescued because of lack of efficacy or who were switched to baricitinib at entry into the long-term extension study showed improved disease responses (CDAI, SDAI, DAS28-ESR) after the switch [112]. On the other hand, patients who are JAKi-IR and cycle to another JAKi were shown to have higher drug survival than patients switched to bDMARDs in an adjusted analysis conducted on data from the SCQM-RA (JAKi vs. TNFi; HR 0.48; 95% CI 0.3 to 0.76) [91] as well as in a pooled international consortium of 17 RA registries, JAK-pot (JAKi vs. bDMARD HR 0.82; 95% CI 0.68 to 0.99; p = 0.04) [95]. Notably, in JAK-pot, it was observed that if the first JAKi was discontinued due to an AE, it was more likely that the second JAKi would also be stopped because of an AE; JAKi cyclers and TNFi switchers showed similar treatment effectiveness [95]. A Japanese study from the FIRST registry reported that JAKi cyclers were more likely than TNFi switchers to achieve CDAI LDA (64.3% vs. 18.8%) and REM (39.3% vs. 0%) [72].

Safety
Due to the chronic nature of RA, patients with high levels of inflammation are at risk of comorbidities including accelerated atherosclerosis [113], VTE [114], malignancy [115] and serious infection [116]. Hence, it is crucial to assess the long-term safety profile of baricitinib, and further studies are required to allow the differentiation between an adverse reaction due to a drug and a comorbidity due to the natural course of the disease.

Baricitinib Safety in RCTs
In 2022, Taylor and colleagues reported on the largest integrated analysis database of baricitinib safety data (from nine Phase III/II/Ib clinical trials and one long-term extension study in RA) that included 3770 patients with RA and over 14,744 patient-years of baricitinib exposure [117]. These patients covered the clinical continuum of RA within the constraints of a clinical trial, and it was demonstrated that AEs were stable over time, with no dose response and no new safety risks observed with prolonged treatment [117]. Moreover, the observed incidence rates of AEs with baricitinib in the RA clinical trials were within the expected range for the typical RA population [118], with the exception of herpes zoster (Figure 3 [76,[117][118][119][120][121]). The most common treatment emergent AEs reported during baricitinib treatment were nasopharyngitis, upper respiratory tract infections, bronchitis, urinary tract infections and herpes zoster [117]. Due to the JAK2 inhibitory effects of baricitinib, laboratory changes were also specifically considered in clinical trials. Investigations showed that changes in neutrophils, lymphocytes, platelets and haemoglobin were generally moderate and usually transient or reversible, infrequently resulting in permanent treatment discontinuation [122]. VTE was, however, considered an adverse drug reaction [9] because of the imbalance observed during the placebo-controlled period of RA-BEAM where six cases of VTE were observed in the baricitinib 4 mg group versus none in the placebo group [123]. Although in one meta-analysis of RCTs, JAKis were not reported to be associated with VTE during the placebo-controlled period [124], another meta-analysis showed that an association was seen at later timepoints [125]. It needs to be remembered when interpreting these data that clinical trials include a highly selected patient population and that the possibility of survivor bias-where people who do not respond to study treatment or who develop an AE would likely discontinue the study-could affect the results of longer-term analyses. tient population and that the possibility of survivor bias-where people who do not respond to study treatment or who develop an AE would likely discontinue the studycould affect the results of longer-term analyses.  [76,[117][118][119][120]. a Herpes zoster incidence is higher in Asia compared to North America and Europe [121]. AEs, adverse events; BARI, baricitinib; excl., excluding; IR, incidence rate; MACE, major adverse cardiovascular events; NMSC, non-melanoma skin cancer; PMS, postmarketing surveillance; PY, patient-years; RA, rheumatoid arthritis; RCT, randomised controlled trial; VTE, venous thromboembolism; YFU, years follow-up.
In a post hoc analysis of baricitinib data pooled from clinical trials and long-term extension studies in RA, it was demonstrated that patients with risk factors (one or more of: age ≥65 years, atherosclerotic CV disease [ASCVD], diabetes mellitus, hypertension, current smoking, high density lipoprotein cholesterol <40 mg/dL, body mass index [BMI] ≥30 kg/m 2 , poor mobility on EQ-5D or history of malignancy) showed an increased incidence of VTE, MACE, malignancy and serious infection as compared to patients without such risk factors [126], highlighting the need to be cautious when treating older patients with risk factors. When other indications for which baricitinib has been investigated are considered (systemic lupus erythematosus, alopecia areata, atopic dermatitis and COVID-19), incidence rates from RCTs for particular AEs are within the range expected for corresponding typical populations with those diseases [118].

New EULAR Recommendations for Risk Management Regarding JAKi Safety
A meta-analysis of data from registries and administrative claims by Salinas and colleagues, discussed in more detail below, reported an increased risk of VTE with baricitinib versus TNFis (IR ratio [IRR] 1.51), and trends towards an increased risk of MACE (IRR 1.54) and serious infection (IRR 1.36) that did not reach significance [33]. Around the time when the results for the ORAL Surveillance [32] and the Salinas publication [33] were shared, several health authorities, including the EMA, reviewed all JAKi data and, based on data from these studies, required an update to the warnings and precautions for all marketed JAKis indicated for inflammatory diseases [127]. Of note, the US Food and Drug Administration (FDA) had already issued JAK-class box warnings in 2021 [128]. These warnings and precautions highlight that, for patients aged over 65 years, present or past smokers and patients presenting with risk factors for MACE, cancer, VTE and serious infections, JAKis should only be used if no suitable alternative treatment is available [127]. The ORAL Surveillance subgroup analysis by age showed an increased risk of malignancies and MACE in patients aged ≥65 years (vs. <65 years), and in these older patients, increased risk in those treated with tofacitinib versus TNFis [32]. In a post hoc analysis of ORAL Surveillance, it was shown that patients with a history of ASCVD are at increased risk of MACE with tofacitinib, whereas in those with no history of ASCVD, no increased risk relative to TNFis was observed [129]. Patients with, versus without, ASCVD were  [76,[117][118][119][120]. a Herpes zoster incidence is higher in Asia compared to North America and Europe [121]. AEs, adverse events; BARI, baricitinib; excl., excluding; IR, incidence rate; MACE, major adverse cardiovascular events; NMSC, non-melanoma skin cancer; PMS, postmarketing surveillance; PY, patient-years; RA, rheumatoid arthritis; RCT, randomised controlled trial; VTE, venous thromboembolism; YFU, years follow-up.
In a post hoc analysis of baricitinib data pooled from clinical trials and long-term extension studies in RA, it was demonstrated that patients with risk factors (one or more of: age ≥65 years, atherosclerotic CV disease [ASCVD], diabetes mellitus, hypertension, current smoking, high density lipoprotein cholesterol <40 mg/dL, body mass index [BMI] ≥30 kg/m 2 , poor mobility on EQ-5D or history of malignancy) showed an increased incidence of VTE, MACE, malignancy and serious infection as compared to patients without such risk factors [126], highlighting the need to be cautious when treating older patients with risk factors. When other indications for which baricitinib has been investigated are considered (systemic lupus erythematosus, alopecia areata, atopic dermatitis and COVID-19), incidence rates from RCTs for particular AEs are within the range expected for corresponding typical populations with those diseases [118].

New EULAR Recommendations for Risk Management Regarding JAKi Safety
A meta-analysis of data from registries and administrative claims by Salinas and colleagues, discussed in more detail below, reported an increased risk of VTE with baricitinib versus TNFis (IR ratio [IRR] 1.51), and trends towards an increased risk of MACE (IRR 1.54) and serious infection (IRR 1.36) that did not reach significance [33]. Around the time when the results for the ORAL Surveillance [32] and the Salinas publication [33] were shared, several health authorities, including the EMA, reviewed all JAKi data and, based on data from these studies, required an update to the warnings and precautions for all marketed JAKis indicated for inflammatory diseases [127]. Of note, the US Food and Drug Administration (FDA) had already issued JAK-class box warnings in 2021 [128]. These warnings and precautions highlight that, for patients aged over 65 years, present or past smokers and patients presenting with risk factors for MACE, cancer, VTE and serious infections, JAKis should only be used if no suitable alternative treatment is available [127]. The ORAL Surveillance subgroup analysis by age showed an increased risk of malignancies and MACE in patients aged ≥65 years (vs. <65 years), and in these older patients, increased risk in those treated with tofacitinib versus TNFis [32]. In a post hoc analysis of ORAL Surveillance, it was shown that patients with a history of ASCVD are at increased risk of MACE with tofacitinib, whereas in those with no history of ASCVD, no increased risk relative to TNFis was observed [129]. Patients with, versus without, ASCVD were more likely to be male, aged ≥65 years, past smokers and have a history of diabetes mellitus, hypertension or hyperlipidaemia. Additionally, a separate post hoc analysis of ORAL Surveillance showed that the risk of MACE, VTE and non-serious infections excluding herpes zoster appeared higher for patients with active disease versus those in REM [130].

Baricitinib Safety from RWE
Most of the RWE studies focusing on baricitinib only sporadically report AEs of special interest and no new safety signals have been identified; the AEs reported correspond to those observed in RCTs. However, this is based on limited data and no analysis involving incidence rates for a given rate of patient-years. The exception is the PMS study of baricitinib use in patients with RA from Japan (55% of patients were aged ≥65 years [mean 64 years]), which reported incidence rates for MACE, VTE and malignancies that were generally similar to those expected in an RA population; the rate of herpes zoster was higher than that expected in an RA population (Figure 3) [76]. This higher rate of herpes zoster with baricitinib versus the RA population has also been observed in RCTs.

Baricitinib vs. TNFi Safety from RWE
RWE safety studies have the advantage of offering longer follow-up and allow comparisons between two or more drugs, but are without randomisation, which implies a higher risk of bias. It is known from the ARTIS Study Group that patients using non-TNFi biologics are older and have a higher disease activity and are less healthy (more likely to have a history of malignancy, serious infection, diabetes and other diseases) than those using TNFis, with the risk that non-TNFi biologics may appear more harmful than TNFis [131]. In line with this, we previously discussed that baricitinib is prescribed to patients who are generally older, with longer disease duration and who have more treatment failures as compared to those prescribed TNFis or b/tsDMARDs other than baricitinib, as highlighted by five studies that investigated effectiveness (statistical testing was not consistently reported) (Tables 2 and 3) [61,62,65,66,77]. Furthermore, in a safety study of data from the French national health data system (Système National des Données de Santé [SNDS]) that compared JAKi users (tofacitinib and baricitinib) to TNFi users (adalimumab), JAKi users were older, with more treatment failure and had numerically higher rates of comorbidities versus TNFi users; however, no formal statistical testing of these data was performed [97]. A recent updated cohort study from the ARTIS Study Group SRQ registry also observed that TNFis are prescribed to patients with less treatment failure, lower disease activity and fewer comorbidities as compared to JAKis, but again no formal testing was performed [79]. An analysis from the JAK-pot study that included >9000 patients treated with JAKi and about 25,000 patients treated with TNFi had similar findings with respect to a higher number of prior b/tsDMARDs and longer disease duration and more comorbidities at JAKi treatment initiation, a finding again not tested statistically [94]. The aforementioned emphasises that patients treated with JAKi are different from patients treated with TNFi. There are statistical approaches available to account for confounding variables and these help to better compare two distinct populations; however, heterogeneity between models used presents advantages and disadvantages and can lead to contradictory results, as discussed here.
Salinas and colleagues (2023) conducted a meta-analysis of real-world data from 14 post-marketing data sources including registries and administrative claims in Europe, the US and Japan [33]. Data regarding patients who experienced a VTE or MACE were mainly accessed from two sources: the Swedish ARTIS Study Group SRQ registry, which accounted for 39% of the total dataset, and a French national health data system (SNDS) that accounted for 32% of the total registry. The meta-analysis showed a trend toward an increased risk of MACE with baricitinib versus TNFis that was importantly driven by data from the SNDS administrative claims database; however, their analysis of data from the ARTIS registry did not show an increased risk. Interestingly, Hoisnard and colleagues (2023) [97] also analysed data from more than 15,000 patients in SNDS and used an alternative method to Salinas and colleagues (2023) [33] (Table 4; Figure 4). Whereas Salinas and colleagues (2023) [33] used propensity score matching to match patients from the two cohorts and remove the remaining patients from the analysis (16% of baricitinib patients), Hoisnard and colleagues (2023) [97] used propensity score weighting to assign patients' outcomes a weight based on their baseline characteristics (age, sex, concomitant csDMARDs or bDMARDs, utilisation of non-steroidal anti-inflammatory drugs [NSAIDS] or glucocorticoids, comorbidities such as obesity and chronic obstructive pulmonary disease [COPD] and history of CV or thromboembolic events within 10 years). Both unweighted and weighted analyses by Hoisnard and colleagues revealed no increase in risk of MACE with baricitinib versus TNFis with a weighted HR of 1.1 [97]. This was also shown in sub-analyses of different populations, such as in patients aged ≥50 years with one CV risk factor, patients aged ≥65 years with one CV risk factor or patients with one CV risk factor. VTE risk assessed by Hoisnard and colleagues (2023) [97] before weighting matched that determined by Salinas and colleagues (2023) [33] and showed an increased risk of VTE with baricitinib; however, after weighting for covariables, the HR for VTE no longer showed an increased risk with baricitinib, in contrast to the findings of Salinas and colleagues (2023) [33].  Figure 4 shows the results of these analyses. b Follow-up was defined as the time to the occurrence of each event (MACE and VTE), death from any cause, exposure discontinuation or 31 December 2021, whichever came first. ARTIS, Anti-Rheumatic Therapy in Sweden; BARI, baricitinib; bDMARD, biologic disease-modifying antirheumatic drug; HR, hazard ratio; IPTW, inverse probability of treatment weighting; JAKi, Janus kinase inhibitor; MACE, major adverse cardiovascular events; NR, not reported; RA, rheumatoid arthritis; SNDS, Système National des Données de Santé (French national health data system); TNFi, tumour necrosis factor inhibitor; tsDMARD, targeted synthetic disease-modifying antirheumatic drug; VTE, venous thromboembolism.
etanercept) and lower than all TNFis investigated in the study, although this w tested statistically [79]. When compared with TNFis (as a class), the risk of VTE creased with baricitinib [80]. Adjusting for covariables is of importance knowing t ease activity, smoking status and comorbidities will have an impact on the risk of VTE, malignancies and serious infection [102][103][104][105].     [33,79,80,97]. b Note that the reported data are from different analyses (weighted HR, adjusted HR and IRR) and therefore cannot be considered directly comparative. The side-by-side presentation is for illustrative purposes only. a All data are for baricitinib versus TNFis, with the exception of the ARTIS MACE analyses for which the comparator was the TNFi etanercept. b Table 4 shows the designs of the reported analyses. c Weighted using inverse probability of treatment weighting method and concomitant administration of MTX as a time-varying variable. Propensity score included age, sex, use of ≥1 csDMARD and use of bDMARD (within two years before index date and at index date), comorbidities (obesity, diabetes, COPD, severe chronic renal disease, dyslipidaemia, hypertension, atherosclerosis of extremities and history of CV or thromboembolic events within 10 years), use of systemic corticosteroids and NSAIDs within two years before index date and at index date, antiplatelet agents, anticoagulants. d Calculated after nearest-neighbour propensity score matching of treatment groups (baricitinib:TNFi) to balance baseline risk factors. Variables considered for inclusion in the propensity score models were risk factors specific to each outcome, including patient demographics, medical history (including comorbidities) and treatments for RA, where available from the original sources. e Weighted using baseline patient characteristics (age, sex, immigrant status, highest achieved education, rheumatoid factor/anti-citrullinated protein antibodies, RA duration, previous b/tsDMARD use, co-medication with conventional synthetic DMARDs and glucocorticosteroids, the 28-joint disease activity score, the Health Assessment Questionnaire-Disability Index, history of malignancy, infections, joint surgery, chronic pulmonary disease, diabetes, cardiovascular disease, depression and the sum of days hospitalized in last five years) from Cox regression adjusted with stabilised inverse probability of treatment weights constructed as the inverse of the predicted probability to have received the treatment actually received, multiplied by the sample proportion with the same treatment. f Estimated using Cox proportional hazards regression, adjusted for age, sex, line of therapy, comorbidities, socioeconomic variables, RA disease variables, civil status and smoking, using an indicator for missing variables. AR-TIS, Anti-Rheumatic Therapy in Sweden; bDMARD, biologic disease-modifying antirheumatic drug; COPD, chronic obstructive pulmonary disease; csDMARD, conventional synthetic disease-modifying antirheumatic drug; CV, cardiovascular; HR, hazard ratio; IRR, incidence rate ratio; MACE, major adverse cardiovascular events; MTX, methotrexate; NSAIDs, non-steroidal anti-inflammatory drugs; RA, rheumatoid arthritis; SNDS, Système National des Données de Santé (French national health data system); TNFi, tumour necrosis factor inhibitor; tsDMARD, targeted-synthetic disease-modifying antirheumatic drug; VTE, venous thromboembolism.
Additional analyses of the ARTIS Study Group SRQ registry data, which unlike administrative claims data reports disease duration and activity, smoking status and medical history (including comorbidities and line of therapy), also assessed individual TNFis and compared them to other mode of action agents, including baricitinib [79,80] (Table 4; Figure 4). No increased risk of MACE with baricitinib compared with each TNFi individually was observed. Additionally, the discontinuation rate due to AEs for patients using baricitinib was significantly lower than that for etanercept (HR 0.57; 95% CI 0.45 to 0.73 vs. etanercept) and lower than all TNFis investigated in the study, although this was not tested statistically [79]. When compared with TNFis (as a class), the risk of VTE was increased with baricitinib [80]. Adjusting for covariables is of importance knowing that disease activity, smoking status and comorbidities will have an impact on the risk of MACE, VTE, malignancies and serious infection [102][103][104][105].
Although there are a few RWE studies of baricitinib that report conflicting results to those of Salinas and colleagues (2022) [33] with regard to MACE, two large, long-term post-marketing RCTs have been initiated to give more information about the risk of this particular event for baricitinib versus TNFi. RA-BRIDGE (NCT03915964) and RA-BRANCH (NCT04086745) are being conducted in >2500 and >1000 participants, respectively, with RA and ≥1 VTE risk factor with an IR or intolerance to ≥1 prior csDMARD or bDMARD. The studies will primarily compare the risk of VTE in patients treated with baricitinib versus TNFi, but are also planned to further inform rheumatologists about any MACE, cancer and serious infection risk for patients using baricitinib.

JAKi Safety from RWE
Three RWE studies have shown an increased risk of VTE in patients treated with JAKis versus TNFis or no JAKi, with data from one registry study [80] and two administrative claims data sets, one of which was a self-controlled case using data from the SNDS [96,98]. In contrast, two other studies did not report an increased risk of VTE with JAKis: one US registry study comparing VTE in tofacitinib versus bDMARDs [132] and a populationbased cohort study, also using data from the SNDS [97]. When MACE was considered, no association was reported with JAKi utilisation in the German RABBIT registry [68], in multivariate analyses of the Argentinian BIOBADASAR 3.0 registry [90] or in an analysis of the SNDS [97] as compared to TNFi users. Analysis of US registry data [132] and administrative claims data [133] did not report an association between MACE and tofacitinib utilisation compared with TNFi/bDMARD utilisation in the overall population, but a trend was observed in an ORAL Surveillance-duplicated cohort in the latter study [133].
Analysis of the Spanish registry, BIOBADASER 3.0, and the Argentinian registry, BIOBADASER 3.0, identified no increased risk of cancer in JAKi users compared with TNFi users [89,90]: a finding similar to that of a study using the SNDS administrative claims data [134]. Another study of administrative claims data investigating the association of tofacitinib and cancer led to similar observations [135]. Serious infections have not been reported to be associated with JAKis in the elderly [93], a finding supported by a study using administrative claims data in Korea; in this analysis, the risk of serious infections was not increased in a JAKi versus a TNFi cohort, with the exception of herpes zoster [136]. Finally, the recent publication from the ARTIS Study Group SRQ registry also showed no increased rate of serious infection with tofacitinib or baricitinib versus etanercept, but an increased rate of herpes zoster infection [79].
In the JAK-pot collaboration of 16 international RA registries with almost 35,000 patients, no increase in drug discontinuation rates due to AEs, a proxy for safety, was observed in the JAKi cohort compared with the TNFi cohort (TNFi vs. JAKi adjusted HR 1.11; 95% CI 0.98 to 1.25) [94].

Risk Assessment for Personalised Medicine for Patients with RA
While it is thought that the future of RA management will be towards personalised medicine based on distinct phenotype and biomarkers [137], current risk mitigation strategies already allow for the prescription of a particular treatment to a specific patient. When TNFis were first used, tuberculosis (TB) was observed at a rate of almost 800 cases/100,000 patientyears in 2002, which dramatically reduced to 38 cases/100,000 patient-years in 2015 after HCPs implemented TB screening in daily practice [138]. Rheumatologists treating patients at risk of demyelination disease, cardiac insufficiency (Type III and IV) and bacterial or viral infections (TB, hepatitis B and opportunist infections) should be cautious when using TNFis [139][140][141][142][143]. IL-6 inhibitors should be avoided for patients with hepatic insufficiency and JAKis should be used with caution in patients aged over 65 years with CV, malignancy or VTE risk factors or recurrent serious infection. JAKis and abatacept have been reported to be effective and safe in patients with RA and interstitial lung disease [144].
Continued observational long-term studies will be required to assess and quantify the safety profile of baricitinib, especially real-world studies in which patients are older, have a longer disease duration and a greater likelihood of having a refractory condition [145]. New EMA warnings and precautions should have an impact on the way rheumatologists prescribe baricitinib. RA-BRIDGE and RA-BRANCH will help the scientific community understand whether the results seen in ORAL Surveillance, in particular those relating to MACE or malignancies, [32] are solely related to tofacitinib or rather, are a JAKi class effect.

Future Directions
Baricitinib has demonstrated rapid efficacy that is consistent in both DMARD pretreated and naïve populations in clinical trials of RA and it has a favourable overall benefit:risk ratio, all of which have been thoroughly confirmed in the context of RWE. Moreover, baricitinib has been shown to be superior to TNFi in randomised clinical trials. In addition, a very recent pragmatic treat-to-target RWE study, which has the advantage of studying baricitinib in real-life but with a randomisation step, confirmed the superiority of baricitinib versus TNFi with regard to the proportion of patients reaching ACR50 at 12 weeks [146]. Furthermore, DAS28-CRP remission rates favoured baricitinib over TNFi at 12 weeks in this study (74% vs. 46%; p < 0.001). However, as in the case of many newly introduced therapies, baricitinib has tended to be used relatively late in the treatment paradigm. There is a compelling case for the earlier introduction of baricitinib in the treatment algorithm with a view to optimising achievable outcomes relating to symptoms and signs as well as patient-reported outcomes. In addition, use of baricitinib rather than a bDMARD as the first b/tsDMARD has been shown to result in lower costs and higher utility over a five-year period in patients with either moderate or severe RA and csDMARD-IR [147]. This approach would also minimise exposure to the drug by older patients with known CV risk factors, in whom the benefit:risk profile of baricitinib (and other JAKi) may be less favourable. If to be used in patients aged ≥65 years, those with moderate renal impairment or those at risk of AEs of special interest (CV events, malignancy, VTE and serious infections), a reduced dosage of baricitinib 2 mg/day is recommended with the possibility to step up to a higher baricitinib dose of 4 mg if RA is not controlled.
As knowledge grows with respect to the pathobiology of RA comorbidities and the relationship to particular mechanisms of action of drugs, it is anticipated that this will inform advances in a more personalised approach to treatment choice and improve the positioning of baricitinib. With indications in RA, alopecia areata, atopic dermatitis and COVID-19, baricitinib is now established as an effective treatment for controlling dysregulated immune responses.
Supplementary Materials: The following supporting information can be downloaded at: https: //www.mdpi.com/article/10.3390/jcm12134527/s1, Table S1: Baseline demographics and characteristics of patients baricitinib-treated patients in real-world settings and RCTs. Funding: This review article was funded by Eli Lilly and Company.

Informed Consent Statement:
This article is based on previously conducted studies and does not contain any new studies with human participants or animals performed by any of the authors.

Data Availability Statement:
No new data were created or analysed in this study. Data sharing is not applicable to this article.