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Review

JAK Inhibitors in the Treatment of T-Cell Lymphomas: Current Evidence and Future Directions

by
Gardenia Taza
,
Naveed Ahmed
and
John L. Vaughn
*
Department of Medicine, NYU Grossman Long Island School of Medicine, Mineola, NY 11501, USA
*
Author to whom correspondence should be addressed.
Cancers 2026, 18(5), 799; https://doi.org/10.3390/cancers18050799
Submission received: 8 January 2026 / Revised: 17 February 2026 / Accepted: 24 February 2026 / Published: 28 February 2026
(This article belongs to the Special Issue T-Cell Lymphoma: From Diagnosis to Treatment)
Versions Notes

Simple Summary

T-cell lymphomas are cancers that originate from white blood cells called T-cell lymphocytes. These cancers can grow slowly or aggressively, and they can affect any part of the body, including the skin and lymph nodes. New treatments are needed for patients with T-cell lymphomas that have become resistant to treatment. Drugs called Janus kinase (JAK) inhibitors may be an effective treatment option for these patients. The first commercially available JAK inhibitor, ruxolitinib, was found to be safe and effective in early-phase clinical trials. Additional JAK inhibitors are currently in clinical development for patients with T-cell lymphomas. Future studies will be needed to determine how well these drugs work in larger groups of patients and to clarify any long-term adverse effects. The purpose of this review is to provide an overview of these medications in the treatment of T-cell lymphomas.

Abstract

T-cell lymphomas are a heterogeneous group of lymphoid neoplasms with a variable prognosis. They can be further divided into cutaneous T-cell lymphomas and peripheral T-cell lymphomas. Treatment options are relatively limited for patients with relapsed or refractory disease. Janus kinase (JAK) inhibitors have emerged as promising new drugs for these lymphomas, as increasing evidence supports the JAK and signal transducer and activator of transcription (STAT) pathway as a potential target. The objective of this review is to summarize the current evidence supporting the use of JAK inhibitors in the treatment of T-cell lymphomas and highlight areas for future research. Although many JAK inhibitors have been developed for the treatment of autoimmune conditions, only a subset of these have been tested in T-cell lymphomas and reported in the literature. These include abrocitinib, cerdulatinib, golidocitinib, ruxolitinib, tofacitinib, and upadacitinib. Other drugs are currently being tested in clinicals trials, including pacritinib and ivarmacitinib, but results are not yet available. Most of the published data are for ruxolitinib, which was found to have a clinical benefit rate of up to 53% in patients with PTCL with activating JAK and/or STAT mutations. Response durations are limited, which may be overcome through combination therapies in the future. JAK inhibitors are associated with multiple adverse effects, including cytopenias and infections, and long-term safety data are lacking for newer agents. Future studies will need to clarify long-term safety and efficacy through well-designed clinical trials involving larger groups of patients.

1. Introduction

T-cell lymphomas (TCLs) represent a large heterogeneous group of lymphoid malignancies originating from T cells or natural killer (NK) cells. The recent fifth edition (2022) of the World Health Organization (WHO-5) recognizes nine families of mature T-cell and NK-cell neoplasms as well as a separate family of precursor T-lymphoblastic neoplasms [1]. In the literature, TCLs are often broadly categorized as either cutaneous T-cell lymphomas (CTCLs), which primarily affect the skin, or peripheral T-cell lymphomas (PTCLs), which include nodal or extranodal subtypes. Among CTCLs, mycosis fungoides (MF) accounts for approximately 50% of cases, while the most common PTCL subtypes include peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS), angioimmunoblastic T-cell lymphoma (AITL), and anaplastic lymphoma kinase (ALK)-positive and ALK-negative anaplastic large cell lymphoma (ALK-positive and ALK-negative ALCL) [2].
Despite their heterogeneity, TCLs are generally more challenging to treat than their B-cell counterparts. Prognosis varies widely across subtypes, from indolent CTCLs to aggressive PTCLs, such as monomorphic epitheliotropic intestinal T-cell lymphoma, which has a median survival of only 7.8 months [3]. Janus kinase (JAK) inhibitors have emerged as promising therapeutic agents, as increasing evidence highlights the JAK/STAT (Janus kinase and signal transducer and activator of transcription) pathway as a potential target in various T-cell lymphomas. Activating mutations of STAT5B and STAT3 were found in γδ-T or NK-cell-derived lymphoma cells, and treatment with a JAK inhibitor caused dose-dependent inhibition of cell growth [4]. In CTCL, point mutations have been detected in JAK1 (0.9%), JAK3 (2.7%), STAT3 (0.9%), and STAT5B (3.6%) [5,6], with JAK3 mutations associated with advanced stage disease and large-cell transformation [6].
Activation of the JAK/STAT pathway has also been observed in other T-cell lymphoproliferative disorders [7,8,9]. In a cohort of 98 cases of PTCL-NOS, 26 exhibited phosphorylated STAT6 (p-STAT6), which was positively correlated with Ki67 expression (p = 0.012) and expression of p52 (p < 0.001). Notably, p-STAT6 expression was related to shorter survival (p = 0.008) [10]. Phosphorylated STAT 3 (p-STAT3) was also associated with decreased overall survival (OS). pSTAT3 was seen within 27% of PTCL-NOS, 29% of angioimmunoblastic T-cell lymphoma (AITL), 93% in ALK-positive ALCL, and 57% in ALK-negative ALCL [11]. Activating mutations in JAK1, JAK2, STAT3, or STAT5B have been noted in 40% of cases of T-cell large granular lymphocytic leukemia (T-LGL) and 75% of T-cell prolymphocytic leukemia [7,9].
JAK inhibitors bind to the enzymatic site of Janus kinases, thereby inhibiting STAT protein phosphorylation and disrupting downstream cytokine-driven signaling pathways [12]. JAK inhibitors are widely used for the treatment of inflammatory diseases such as rheumatoid arthritis or ulcerative colitis [13]. Some JAK inhibitors have been approved for the treatment of myelofibrosis and polycythemia vera [14]. However, there are no US Federal Drug Administration (FDA)-approved JAK inhibitors for T-cell lymphomas. To date, ruxolitinib is the sole agent approved for the treatment of chronic graft-versus-host disease (cGVHD), a post-stem-cell transplant complication that may arise in some individuals with lymphoma [15]. The aim of this review is to provide an overview of JAK inhibitors in the management of T-cell lymphomas. We will discuss six JAK inhibitors, including preliminary efficacy and notable adverse effects, omitting some inhibitors such as baricitinib due to lack of data in this patient population.

2. Ruxolitinib

Ruxolitinib is a selective JAK1 and JAK2 inhibitor. It is available in both topical and oral formulations. Its oral formulation is currently approved for the treatment of steroid-refractory acute graft-versus-host disease (aGVHD) and chronic graft-versus-host disease (cGVHD) in adults and pediatric patients 12 years and older [16,17]. aGVHD and cGVHD are potential complications in T-cell lymphoma patients who have undergone allogeneic hematopoietic cell transplantation (HCT) [18,19]. For aGVHD, doses start at 5 mg twice daily, and for cGVHD, doses start at 10 mg twice daily.
Ruxolitinib has been used to achieve disease control and to bridge to allogeneic HCT, leading to a durable remission [20]. Jaramillo et al. describe a patient with cutaneous relapsed T-cell acute lymphoblastic leukemia (T-ALL) with JAK3 mutations following an allogeneic blood cell transplant [21]. Given major contraindications to tofacitinib (JAK1, JAK2, JAK3 inhibitor), combination therapy with tofacitinib and ruxolitinib was not pursued. Instead, salvage therapy with ruxolitinib monotherapy showed complete remission of skin lesions at day 50. Ruxolitinib was then discontinued after 5 months due to cutaneous relapse [21]. Cao et al. describe a patient with chronic diarrhea, found to have indolent T-cell lymphoma of the gastrointestinal tract (ITCL-GI) with a STAT3::JAK2 fusion. His diarrhea resolved after 3 months of ruxolitinib 10 mg twice daily. Despite his clinical improvement, repeat endoscopy did not show any changes in histomorphologic changes [22].
A retrospective review of 6 patients treated with ruxolitinib (4 oral and 2 topical) found a clinical response in 3 cases. A patient with CTCL treated with oral ruxolitinib had a complete response for 3 years, while another patient with subcutaneous panniculitis-like T-cell lymphoma (SPTCL) with a JAK2 point mutation showed diminishing lesions for a year. Plaque thinning was seen in a patient with MF on topical ruxolitinib. Notably, oral ruxolitinib doses varied across patients from 5 mg twice daily to 20 mg twice daily [23]. Levy et al. reported a case of a 16-year-old male with relapsing hemophagocytic lymphohistiocytosis and SPTCL who achieved remission in 4 months with ruxolitinib 15 mg twice daily. Ruxolitinib was self-tapered and discontinued by the patient, with disease relapse noted 8 months after discontinuation. Ruxolitinib was then re-initiated with eventual complete remission [24].
In a phase 2 biomarker-driven study, 45 patients with PTCL and 7 patients with MF received ruxolitinib 20 mg twice daily on a 28-day cycle. Patients were placed in one of three cohorts: (1) patients whose tumors had activating JAK and/or STAT mutations; (2) patients whose tumors lacked mutations but exhibited ≥30% pSTAT3 expression by immunohistochemistry; or (3) patients whose tumors did not meet either criterion. Clinical benefit response (CBR) was defined as complete response (CR), partial response (PR), or stable disease for 6 months. The CBR of PTCL and CTCL in cohorts 1, 2, and 3 were 48%, 36%, and 18%, respectively. Only 1 of 7 MF patients achieved PR, and notably, their tumor only exhibited 20% of pSTAT3 expression. A total of 8 patients (15% of cases) achieved responses of greater than 1 year, including 4 of 5 T-LGL, 1 PTCL-NOS, 1 with AITL, 1 with primary cutaneous ALCL, and 1 with MF. This study suggests that in PTCL and non-MF CTCL, JAK/STAT mutations and/or pSTAT3 expression in ≥30% of tumor cells predicted CBR to ruxolitinib (p = 0.02) [25].

3. Tofacitinib

Tofacitinib, a JAK1, JAK2, and JAK3 inhibitor, is currently approved for select autoimmune conditions such as rheumatoid arthritis, psoriatic arthritis, and ulcerative colitis, among others. Tofacitinib has been increasingly utilized off-label in the treatment of various dermatological conditions, including cutaneous manifestations of autoimmune conditions [26]. Studies investigating the effectiveness of tofacitinib in T-cell lymphomas remain largely preclinical. In one study, tofacitinib was shown to inhibit tumor growth in EBV-associated T-cell lymphoma cells [27].
Suhl et al. reported successful treatment of a patient with cutaneous sarcoidosis and Sézary syndrome using a combination of tofacitinib and romidepsin [28]. Romidepsin is a histone deacetylase inhibitor with FDA approval for CTCL. Although romidepsin monotherapy initially led to improvement, the patient’s condition plateaued after one month. The addition of tofacitinib resulted in reduced generalized erythema, minimal skin tenderness, and the resolution of axillary and inguinal lymphadenopathy [25]. A treatment regimen of tofacitinib and ruxolitinib was also successful in a patient with T-PLL with relapsed disease 16 months after undergoing a stem cell transplant. Targeted next-generation sequencing identified two missense JAK3 mutations. In vitro studies showed that the combination of tofacitinib and ruxolitinib exhibited a synergistic effect in leukemic cells. This patient was initially started on tofacitinib 5 mg twice daily, further increased to 10 mg twice daily after 15 days of treatment. Ruxolitinib was added one month after initiating tofacitinib, and within the first two months of dual therapy, there was an improvement in fatigue, low-grade fevers, night sweats, and a regression of leukemia cutis lesions [29].

4. Golidocitinib

Golidocitinib is a selective JAK1 inhibitor currently under active investigation specifically for the treatment of PTC [30]. The rationale for targeting JAK1 alone is that selective JAK1 inhibition may result in lower toxicity [31].
JACKPOT8 part B, a multinational phase 2 single-arm trial, is currently the largest active trial at the time of this review’s writing [31]. Patients ≥ 18 years of age with relapsed/refractory PTCL who had received at least 1 prior line of therapy and had an Eastern Cooperative Oncology Group (ECOG) performance status of 0–2 met the inclusion criteria. Patients received oral golidocitinib 150 gm once daily until disease progression or other discontinuation criteria were met. A total of 104 patients were enrolled between 26 February 2021 and 12 October 2022. Median follow-up was 13.3 months. As of the most recent update in January of 2024, the objective response rate was 44.3%, with 24% of patients achieving CR and 21% of patients achieving PR. The primary grade 3 and 4 adverse effects observed have been neutropenia and thrombocytopenia. To date, 1 event of death has been recorded secondary to fungal pneumonia thought to be secondary to golidocitinib-induced immunosuppression [31].
Golidocitinib received conditional approval in China based on the results of JACKPOT8. The full therapeutic potential of golidocitinib continues to be assessed in ongoing studies. A phase 2 study (NCT05963347) is evaluating the combination of golidocitinib with CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone) in newly diagnosed PTCL. A separate clinical trial (NCT06733051) for extranodal Natural Killer/T-cell lymphoma is exploring the efficacy of golidocitinib and benmelstobart, an anti-PD-L1 inhibitor, in patients with relapsed or refractory disease.

5. Cerdulatinib

Cerdulatinib is an experimental dual inhibitor of spleen tyrosine kinase (SYK), JAK1, JAK2, and JAK3. It is being widely tested in hematological malignancies and dermatological conditions. A preclinical study in adult T-cell leukemia/lymphoma found that cerdulatinib suppressed cell proliferation and cell viability more than pan-JAK or SYK-selective inhibitors alone. Furthermore, murine models treated with cerdulatinib resulted in lower tumor burden [32].
An expansion phase II study of 98 patients with refractory PTCL or CTCL treated with cerdulatinib 30 mg orally twice daily noted good tolerability and favorable responses. An interim analysis demonstrated an ORR of 35% in CTCL patients [33,34]. Responses in MF and SS varied greatly, with an ORR of 45% and an ORR of 17%, respectively. No patients with SS achieved a complete response, whereas 9% of MF patients did. However, in CTCL patients, rapid improvement in pruritus was observed, independent of tumor response. At study conclusion, the ORR was 51.9% in the angioimmunoblastic T-cell lymphoma and T follicular helper cell lymphoma (AITL/TFH) subgroup, 31.8% for other histological subtypes, and a surprising 0% for PTCL-NOS. In the AITL/TFH subgroup, complete remission was achieved in 10 patients and partial remission in 4 patients. These responses were generally maintained for more than 6 months, with five patients showing persistent responses for more than 12 months. Adverse effects included lipase and amylase increases (with no clinical pancreatitis), diarrhea, neutropenia, anemia, and fatigue, all of which were treated by standard care [33,34].

6. Upadacitinib

Upadacitinib is a selective JAK1 inhibitor with FDA-approval for a range of chronic inflammatory diseases. Upadacitinib has been used off-label for CTCL in select case studies.
Castillo et al. describe a case of erythrodermic mycosis fungoides treated successfully with upadacitinib. Initial skin biopsies were inconclusive, and in the absence of significant lymphadenopathy, a diagnosis of atopic dermatitis was made. The patient was started on upadacitinib 15 mg daily. After 2 months, repeat biopsies confirmed MF stage 3. By week 16, the patient achieved complete response with less than 10% of body surface area affected [35]. Another case of MF misdiagnosed as atopic dermatitis found notable improvement in both skin lesions and pruritus within two weeks of initiating upadacitinib [36].

7. Abrocitinib

Abrocitinib is a selective JAK1 inhibitor approved for moderate to severe atopic dermatitis. It is currently being investigated for other dermatological, allergic, and inflammatory conditions. There is only one case noting abrocitinib in combination with interferon and phototherapy to treat a refractory case of recalcitrant folliculotropic MF. The initiation of abrocitinib led to significant improvement in pruritus within four weeks, and a noticeable reduction in plaques and papules was observed after three months [37].

8. Safety of JAK Inhibitors

In clinical trials, JAK inhibitors were associated with multiple adverse events. In patients with PTCL and MF who were treated with ruxolitinib, common adverse events (occurring in greater than 5% of patients) were anemia, neutropenia, thrombocytopenia, diarrhea, fatigue, and febrile neutropenia [25]. Golidocitinib was associated with neutropenia, thrombocytopenia, increased transaminases, pneumonia, and leukopenia. For cerdulatinib, the most common treatment-emergent adverse events were increased amylase, diarrhea, nausea, increased lipase, and fatigue [34]. A list of adverse effects associated with JAK inhibitors is shown in Table 1. In these trials, adverse events requiring discontinuation of the treatments were uncommon. For example, in the JACKPOT8 trial, only 9% of patients treated with golidocitinib discontinued the drug due to treatment-emergent adverse events [31].
In 2021, the FDA published a warning that JAK inhibitors might be linked to a higher incidence of lymphomas and other malignancies [42]. This warning was based on the ORAL surveillance study, which compared the risk of cardiac events, malignancy, and infection in patients with rheumatoid arthritis receiving tofacitinib with those receiving a tumor necrosis factor inhibitor [43]. Since other JAK inhibitors work through similar pathways, the warning was extended to the entire drug class [44]. Several cases have been reported in the literature, as described below [45,46,47,48,49,50].
Cohen et al. described two cases of severe CTCL relapse in patients treated with ruxolitinib for cGVHD after allogeneic HCT. Both individuals presented with relapsed MF, notable for erythroderma and extensive skin tumors, with blood involvement in one case [45].
Knapp et al. reported a case of refractory erythema elevatum diutinum treated with tofacitinib. The patient ultimately developed lymphomatoid papulosis (LyP) with ocular involvement after 8 weeks of treatment [46].
Linuma et al. described a case of LyP in a patient treated with upadacitinib for rheumatoid arthritis. Her presentation was notable for red-to-brown papules on her extremities two weeks after upadacitinib initiation. The authors suggested that the immunosuppression from JAK1 inhibition increased her susceptibility to LyP. Her lesions improved with upadacitinib discontinuation and topical corticosteroids [47].
Mo et al. reported a patient with severe atopic dermatitis, who was started on upadacitinib with partial relief of his symptoms. His course was complicated by multiple episodes of bullous impetigo, leading to discontinuation of upadacitinib and rapid deterioration of his symptoms. One month after upadacitinib discontinuation, the patient underwent a cheek biopsy that revealed pilotropic MF [48].
Lamolet et al. described a patient with early MF who was misdiagnosed as atopic dermatitis and treated with upadacitinib and baricitinib (another JAK1/JAK2 inhibitor that has not been studied in lymphoma patients). Despite an initial brief improvement in symptoms, the patient was noted to have worsening skin lesions and the development of inguinal lymphadenopathy, which the authors attributed to JAK inhibitor use [49]. A similar transient response with eventual worsening disease was also noted by Martin-Torregrosa et al. in a patient treated with upadacitinib [50].
In 2025, a retrospective cohort study identified cases of CTCL following exposure to dupilumab (anti-IL-4Rα), tralokinumab (anti- IL-13), or JAK inhibitors. They identified no patients diagnosed with CTCL following treatment with JAK inhibitors alone or tralokinumab alone [51]. It remains unclear whether JAK inhibitors cause secondary malignancies (e.g., through their immunosuppressive effects) or if the observed associations are due to confounding.

9. Conclusions and Future Directions

T-cell lymphomas remain challenging diseases to treat due to relatively limited treatment options, especially in the relapsed/refractory setting [52]. Relapsed/refractory T-cell lymphomas are associated with poor outcomes, emphasizing the need for novel therapies. Activation of the JAK/STAT pathway has emerged as a driver in the pathogenesis of multiple T-cell lymphoma subtypes, providing a compelling rationale for JAK inhibitor use. However, more data from clinical trials are needed in order to support their use as standard therapies. Table 2 shows a list of ongoing clinical trials that are testing JAK inhibitors in the treatment of T-cell lymphomas. Many of the trials involve the use of combination therapies, including the use of JAK inhibitors in the frontline setting. Ruxolitinib and golidocitinib are both being tested in separate trials in combination with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) for newly diagnosed peripheral T-cell lymphomas.
Among the commercially available JAK inhibitors, ruxolitinib has the most published data for the treatment of T-cell lymphomas. Ruxolitinib has demonstrated favorable responses across both CTCL and PTCL, especially in patients with activating JAK/STAT mutation or elevated pSTAT3 expression [25]. However, response durations have been limited. Combination with BCL-2 or PI3K inhibitors highlights a potential strategy to overcome possible resistance mechanisms [53]. Another area for future research will be to determine whether one type of JAK inhibitor is preferred over another for certain T-cell lymphoma subtypes.
In addition to promoting objective disease responses, JAK inhibitors may also have a role in the amelioration of symptoms. JAK inhibitors improve symptoms, including erythema, pruritus, and cytopenias. The use of oral JAK inhibitors for symptomatic improvement alone may be a particularly attractive option for patients with indolent T-cell lymphomas such as mycosis fungoides, perhaps in combination with topical JAK inhibitors [54]. Additional clinical trials using standardized quality of life measures will help support the role of JAK inhibitors for these diseases.
The FDA has raised concerns regarding the safety of JAK inhibitors and the potential increased risk of cancer in patients who receive these medications for autoimmune diseases. However, a causal association between JAK inhibitors and malignancy has not been established. Autoimmune disease itself is associated with an increased risk of lymphoma, representing a possible source of confounding. A recent retrospective study did not find any cases of CTCL in treatment with JAK inhibitors alone, contradicting other case reports [51].
In conclusion, JAK inhibitors are generally well-tolerated drugs that may offer meaningful clinical responses, either through disease control or symptomatic improvement in patients with T-cell lymphomas. These drugs are being further tested as part of combination therapies, including in patients with newly diagnosed T-cell lymphomas. Further research should focus on patient selection through biomarker-driven approaches and combination strategies to enhance therapeutic efficacy and durability.

Author Contributions

Conceptualization, J.L.V.; writing—original draft preparation, G.T. and N.A.; Writing—review and editing, J.L.V. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
aGVHDAcute graft-versus-host disease
cGVHDChronic graft-versus-host disease
CHOPCyclophosphamide, doxorubicin, vincristine, and prednisone
CTCLCutaneous T-cell lymphoma
FDAFood and Drug Administration
HCTHematopoietic cell transplantation
JAKJanus kinase
MFMycosis fungoides
NKNatural Killer
PTCLPeripheral T-cell lymphoma
STATSignal transducer and activator of transcription
T-ALLT-cell acute lymphoblastic leukemia

References

  1. Alaggio, R.; Amador, C.; Anagnostopoulos, I. The 5th edition of the World Health Organization Classification of haematolymphoid tumours: Lymphoid neoplasms. Leukemia 2022, 36, 1720–1748, Erratum in Leukemia 2023, 37, 1944–1951. [Google Scholar] [CrossRef]
  2. Horwitz, S.M.; Zelenetz, A.D.; Gordon, L.I.; Wierda, W.G.; Abramson, J.S.; Advani, R.H.; Andreadis, C.B.; Bartlett, N.; Byrd, J.C.; Fayad, L.E.; et al. NCCN Guidelines Insights: Non-Hodgkin’s Lymphomas, Version 3.2016. J. Natl. Compr. Cancer Netw. 2016, 14, 1067–1079. [Google Scholar] [CrossRef]
  3. Veloza, L.; Cavalieri, D.; Missiaglia, E.; Ledoux-Pilon, A.; Bisig, B.; Pereira, B.; Bonnet, C.; Poullot, E.; Quintanilla-Martinez, L.; Dubois, R.; et al. Monomorphic epitheliotropic intestinal T-cell lymphoma comprises morphologic and genomic heterogeneity impacting outcome. Haematologica 2023, 108, 181–195. [Google Scholar] [CrossRef]
  4. Kucuk, C.; Jiang, B.; Hu, X.; Zhang, W.; Chan, J.K.; Xiao, W.; Lack, N.; Alkan, C.; Williams, J.C.; Avery, K.N.; et al. Activating mutations of STAT5B and STAT3 in lymphomas derived from gammadelta-T or NK cells. Nat. Commun. 2015, 6, 6025. [Google Scholar] [CrossRef]
  5. Park, J.; Yang, J.; Wenzel, A.T.; Ramachandran, A.; Lee, W.J.; Daniels, J.C.; Kim, J.; Martinez-Escala, E.; Amankulor, N.; Pro, B.; et al. Genomic analysis of 220 CTCLs identifies a novel recurrent gain-of-function alteration in RLTPR (p.Q575E). Blood 2017, 130, 1430–1440. [Google Scholar] [CrossRef]
  6. Pérez, C.; Mondéjar, R.; García-Díaz, N.; Cereceda, L.; León, A.; Montes, S.; Durán Vian, C.; Pérez Paredes, M.G.; González-Morán, A.; Miguel, V.; et al. Advanced-stage mycosis fungoides: Role of the signal transducer and activator of transcription 3, nuclear factor-κB and nuclear factor of activated T cells pathways. Br. J. Dermatol. 2020, 182, 147–155. [Google Scholar] [CrossRef]
  7. Kiel, M.J.; Velusamy, T.; Rolland, D.; Sahasrabuddhe, A.A.; Chung, F.; Bailey, N.G.; Schrader, A.; Li, B.; Li, J.Z.; Ozel, A.B.; et al. Integrated genomic sequencing reveals mutational landscape of T-cell prolymphocytic leukemia. Blood 2014, 124, 1460–1472. [Google Scholar] [CrossRef]
  8. Koskela, H.L.; Eldfors, S.; Ellonen, P.; van Adrichem, A.J.; Kuusanmaki, H.; Andersson, E.I.; Lagstrom, S.; Clemente, M.J.; Olson, T.; Jalkanen, S.E.; et al. Somatic STAT3 mutations in large granular lymphocytic leukemia. N. Engl. J. Med. 2012, 366, 1905–1913. [Google Scholar] [CrossRef]
  9. Jerez, A.; Clemente, M.J.; Makishima, H.; Koskela, H.; Leblanc, F.; Peng Ng, K.; Olson, T.; Przychodzen, B.; Afable, M.; Gomez-Segui, I.; et al. STAT3 mutations unify the pathogenesis of chronic lymphoproliferative disorders of NK cells and T-cell large granular lymphocyte leukemia. Blood 2012, 120, 3048–3057. [Google Scholar] [CrossRef]
  10. Manso, R.; Sánchez-Beato, M.; González-Rincón, J.; Gómez, S.; Rojo, F.; Mollejo, M.; García-Cosio, M.; Menárguez, J.; Piris, M.A.; Rodríguez-Pinilla, S.M. Mutations in the JAK/STAT pathway genes and activation of the pathway, a relevant finding in nodal Peripheral T-cell lymphoma. Br. J. Haematol. 2018, 183, 497–501. [Google Scholar] [CrossRef]
  11. Han, J.J.; O’Byrne, M.; Stenson, M.J.; Maurer, M.J.; Wellik, L.E.; Feldman, A.L.; McPhail, E.D.; Witzig, T.E.; Gupta, M. Prognostic and therapeutic significance of phosphorylated STAT3 and protein tyrosine phosphatase-6 in peripheral-T cell lymphoma. Blood Cancer J. 2018, 8, 110. [Google Scholar] [CrossRef]
  12. Lin, C.M.; Cooles, F.A.; Isaacs, J.D. Basic Mechanisms of JAK Inhibition. Mediterr. J. Rheumatol. 2020, 31, 100–104. [Google Scholar] [CrossRef]
  13. Tanaka, Y.; Luo, Y.; O’Shea, J.J.; Nakayamada, S. Janus kinase-targeting therapies in rheumatology: A mechanisms-based approach. Nat. Rev. Rheumatol. 2022, 18, 133–145. [Google Scholar] [CrossRef]
  14. Constantinescu, S.N.; Vainchenker, W.; Pecquet, C. Next-Generation JAK Inhibitors in the Treatment of Myeloproliferative Neoplasms. Blood 2026. [Google Scholar] [CrossRef]
  15. Kashyap, A.; Dai, J.; Ni, X. Therapeutic Targeting of the Janus Kinase/Signal Transducer and Activator of Transcription Pathway in Cutaneous T-Cell Lymphoma. Cancers 2025, 17, 568. [Google Scholar] [CrossRef]
  16. Zeiser, R.; Polverelli, N.; Ram, R.; Hashmi, S.K.; Chakraverty, R.; Middeke, J.M.; Musso, M.; Giebel, S.; Uzay, A.; Langmuir, P.; et al. Ruxolitinib for Glucocorticoid-Refractory Chronic Graft-versus-Host Disease. N. Engl. J. Med. 2021, 385, 228–238. [Google Scholar] [CrossRef]
  17. Zeiser, R.; von Bubnoff, N.; Butler, J.; Mohty, M.; Niederwieser, D.; Or, R.; Szer, J.; Wagner, E.M.; Zuckerman, T.; Mahuzier, B.; et al. Ruxolitinib for Glucocorticoid-Refractory Acute Graft-versus-Host Disease. N. Engl. J. Med. 2020, 382, 1800–1810. [Google Scholar] [CrossRef]
  18. Zeiser, R.; Blazar, B.R. Acute Graft-versus-Host Disease—Biologic Process, Prevention, and Therapy. N. Engl. J. Med. 2017, 377, 2167–2179. [Google Scholar] [CrossRef]
  19. Pidala, J.A.; Gooley, T.A.; Luznik, L.; Blazar, B.R. Chronic graft-versus-host disease: Unresolved complication or ancient history? Blood 2024, 144, 1363–1373. [Google Scholar] [CrossRef]
  20. Watson, L.R.; Lew, T.E.; Fox, L.C.; Khot, A.; Weyden, C. Ruxolitinib bridging therapy to allogeneic SCT for high-risk refractory subcutaneous panniculitis-like T-cell lymphoma. Leuk. Lymphoma 2022, 63, 3217–3221. [Google Scholar] [CrossRef]
  21. Jaramillo, S.; Hennemann, H.; Horak, P.; Teleanu, V.; Heilig, C.E.; Hutter, B.; Stenzinger, A.; Glimm, H.; Goeppert, B.; Müller-Tidow, C.; et al. Ruxolitinib is effective in the treatment of a patient with refractory T-ALL. EJHaem 2020, 2, 139–142. [Google Scholar] [CrossRef]
  22. Cao, X.; Mulroney, C.; Wang, H.Y. Treatment of an Indolent T-Cell Lymphoma of the Gastrointestinal Tract Harboring STAT3::JAK2 with Jakafi (Ruxolitinib) with Significant Clinical Improvements. EJHaem 2025, 6, e70047. [Google Scholar] [CrossRef]
  23. Liao, V.; Lavin, L.; Ong, M.M.; Pulitzer, M.P.; Moskowitz, A.J.; Myskowski, P.L.; Geller, S. Oral and Topical Janus Kinase Inhibitors in Patients with Cutaneous T-Cell Lymphoma: A Real-World Single-Center Experience. J. Dermatol. 2025, 52, 1107–1112. [Google Scholar] [CrossRef]
  24. Lévy, R.; Fusaro, M.; Guerin, F.; Chetouani, A.; Moshous, D.; Fischer, A.; Basile, G.; Sepulveda, F.E.; Neven, B. Efficacy of ruxolitinib in subcutaneous panniculitis-like T-cell lymphoma and hemophagocytic lymphohistiocytosis. Blood Adv. 2020, 4, 1383–1387, Erratum in Blood Adv. 2023, 7, 800. [Google Scholar] [CrossRef]
  25. Moskowitz, A.J.; Ghione, P.; Jacobsen, E.; Ruan, J.; Schatz, J.H.; Noor, S.; Myskowski, P.; Vardhana, S.; Ganesan, N.; Hancock, H.; et al. A phase 2 biomarker-driven study of ruxolitinib demonstrates effectiveness of JAK/STAT targeting in T-cell lymphomas. Blood 2021, 138, 2828–2837. [Google Scholar] [CrossRef]
  26. Tegtmeyer, K.; Zhao, J.; Maloney, N.J.; Atassi, G.; Beestrum, M.; Lio, P.A. Off-label studies on tofacitinib in dermatology: A review. J. Dermatol. Treat. 2021, 32, 399–409. [Google Scholar] [CrossRef]
  27. Ando, S.; Kawada, J.I.; Watanabe, T.; Suzuki, M.; Sato, Y.; Torii, Y.; Asai, M.; Goshima, F.; Murata, T.; Shimizu, N.; et al. Tofacitinib induces G1 cell-cycle arrest and inhibits tumor growth in Epstein-Barr virus-associated T and natural killer cell lymphoma cells. Oncotarget 2016, 7, 76793–76805. [Google Scholar] [CrossRef]
  28. Suhl, S.; Lapolla, B.; Kaminsky, A.; Geskin, L.J. Treatment of Sezary syndrome with combination romidepsin and tofacitinib: A case report. JAAD Case Rep. 2024, 55, 69–72. [Google Scholar] [CrossRef]
  29. Gomez-Arteaga, A.; Margolskee, E.; Wei, M.T.; Besien, K.; Inghirami, G.; Horwitz, S. Combined use of tofacitinib (pan-JAK inhibitor) and ruxolitinib (a JAK1/2 inhibitor) for refractory T-cell prolymphocytic leukemia (T-PLL) with a JAK3 mutation. Leuk. Lymphoma 2019, 60, 1626–1631. [Google Scholar] [CrossRef]
  30. Song, Y.; Yoon, D.H.; Yang, H.; Cao, J.; Ji, D.; Koh, Y.; Jing, H.; Eom, H.; Kwak, J.; Lee, W.; et al. Phase I dose escalation and expansion study of golidocitinib, a highly selective JAK1 inhibitor, in relapsed or refractory peripheral T-cell lymphomas. Ann. Oncol. Off. J. Eur. Soc. Med. Oncol. 2023, 34, 1055–1063. [Google Scholar] [CrossRef]
  31. Song, Y.; Malpica, L.; Cai, Q.; Zhao, W.; Zhou, K.; Wu, J.; Zhang, H.; Mehta-Shah, N.; Ding, K.; Liu, Y.; et al. Golidocitinib, a selective JAK1 tyrosine-kinase inhibitor, in patients with refractory or relapsed peripheral T-cell lymphoma (JACKPOT8 Part B): A single-arm, multinational, phase 2 study. Lancet Oncol. 2024, 25, 117–125. [Google Scholar] [CrossRef]
  32. Ishikawa, C.; Senba, M.; Mori, N. Anti-adult T-cell leukemia/lymphoma activity of cerdulatinib, a dual SYK/JAK kinase inhibitor. Int. J. Oncol. 2018, 53, 1681–1690. [Google Scholar] [CrossRef]
  33. Horwitz, S.M.; Feldman, T.A.; Hess, B.T.; Khodadoust, M.S.; Kim, Y.H.; Munoz, J.; Patel, M.R.; Phillips, T.J.; Smith, S.D.; Smith, S.M. A phase 2 study of the dual SYK/JAK inhibitor cerdulatinib demonstrates good tolerability and clinical response in relapsed/refractory peripheral T-cell lymphoma and cutaneous T-cell lymphoma. Blood 2019, 134, 466. [Google Scholar] [CrossRef]
  34. Horwitz, S.M.; Feldman, T.A.; Ye, J.C.; Khodadoust, M.S.; Munoz, J.; Hamlin, P.A.; Kim, Y.H.; Wilcox, R.A.; Patel, M.R.; Coffey, G.; et al. Results from an open-label phase 2a study of cerdulatinib, a dual spleen tyrosine kinase/janus kinase inhibitor, in relapsed/refractory peripheral T-cell lymphoma. Leuk Lymphoma 2025, 66, 1100–1110. [Google Scholar] [CrossRef]
  35. Castillo, D.E.; Romanelli, P.; Lev-Tov, H.; Kerdel, F. A case of erythrodermic mycosis fungoides responding to upadacitinib. JAAD Case Rep. 2022, 30, 91–93. [Google Scholar] [CrossRef] [PubMed]
  36. Kook, H.; Park, S.Y.; Hong, N.; Lee, D.H.; Jung, H.J.; Park, M.Y.; Ahn, J. Severely pruritic mycosis fungoides successfully treated with upadacitinib. J. Dtsch. Dermatol. Ges. 2024, 22, 450–451. [Google Scholar] [CrossRef] [PubMed]
  37. Liu, Z.; Huang, Q.; Ding, T.; Lin, J. A case of recalcitrant folliculotropic mycosis fungoides successfully treated by abrocitinib. Int. J. Dermatol. 2025, 64, 751–753. [Google Scholar] [CrossRef] [PubMed]
  38. Incyte Corporation. Ruxolitinib Prescribing Information. 2011. Available online: https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/202192lbl.pdf (accessed on 5 January 2026).
  39. Pfizer Corportation. Tofacitinib Prescribing Information. 2018. Available online: https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/203214s018lbl.pdf (accessed on 5 January 2026).
  40. AbbVie Corportation. Upadacitinib Prescribing Information. 2022. Available online: https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/211675s003lbl.pdf (accessed on 5 January 2026).
  41. Pfizer Corportation. Abrocitinib Prescribing Information. 2023. Available online: https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/213871s001lbl.pdf (accessed on 5 January 2026).
  42. Murphrey, M.; Waldman, R.A.; Durso, T.; Grant-Kels, J.M. Special editorial: When prescribing Janus kinase inhibitors for dermatologic conditions, be mindful of the Food and Drug Administration’s September 1, 2021, data safety communication. J. Am. Acad. Dermatol. 2022, 86, 42–43. [Google Scholar] [CrossRef]
  43. Ytterberg, S.R.; Bhatt, D.L.; Mikuls, T.R.; Koch, G.G.; Fleischmann, R.; Rivas, J.L.; Germano, R.; Menon, S.; Sun, Y.; Wang, C.; et al. Cardiovascular and Cancer Risk with Tofacitinib in Rheumatoid Arthritis. N. Engl. J. Med. 2022, 386, 316–326. [Google Scholar] [CrossRef]
  44. The Lancet Rheumatology. JAK inhibitors-Friend or Foe? Lancet Rheumatol. 2024, 6, e129. [Google Scholar] [CrossRef]
  45. Cohen, E.; Bozonnat, A.; Battistella, M.; Calvani, J.; Vignon-Pennamen, M.D.; Rivet, J.; Moins-Teisserenc, H.; Ta, V.A.; Ram-Wolff, C.; Bouaziz, J.D.; et al. Severe relapses of cutaneous T-cell lymphoma after treatment of chronic graft-versus-host disease with ruxolitinib. J. Eur. Acad. Dermatol. Venereol. 2024, 38, pe32. [Google Scholar] [CrossRef]
  46. Knapp, C.; Steele, E.; Mengden-Koon, S.; Williams, T.; Fett, N. A Case of Tofacitinib-Induced Lymphomatoid Papulosis with Ocular Involvement. Am. J. Dermatopathol. 2022, 44, 523–525. [Google Scholar] [CrossRef]
  47. Iinuma, S.; Hayashi, K.; Noguchi, A.; Ishida-Yamamoto, A. Lymphomatoid papulosis during upadaci-tinib treatment for rheumatoid arthritis. Eur. J. Dermatol. 2022, 32, 142–143. [Google Scholar] [CrossRef]
  48. Mo, S.; Friedmann, D. Cutaneous T-cell lymphoma in a JAK inhibitor patient: A case report. SAGE Open Med Case Rep. 2024, 12, 2050313X241231491. [Google Scholar] [CrossRef]
  49. Lamolet, M.; Barbarin, C.; Renaud, O.; Sahin, Y.; Wierzbicka-Hainaut, E.; Masson Regnault, M. Acceleration of cutaneous T-cell lymphoma mistaken for atopic dermatitis following JAK inhibitor use. Eur. J. Dermatol. 2023, 33, 686–687. [Google Scholar] [CrossRef]
  50. Martín-Torregrosa, D.; Torres-Navarro, I.; Mansilla-Polo, M.; Alonso-Fernández, G.; Fayos-Gregori, R.; Cózar, V.M.I.; Botella-Estrada, R. Cutaneous T-cell lymphomas initially diagnosed as inflammatory dermatoses and treated with biologics and small molecules. J. Dtsch. Dermatol. Ges. 2025, 24, 91–95. [Google Scholar] [CrossRef]
  51. Liao, V.; Lavin, L.; Pulitzer, M.P.; Stuver, R.; Geller, S. Diagnosis of cutaneous T-cell lymphoma following exposure to biologic agents for atopic dermatitis: A retrospective cohort study from a single tertiary cancer center. J. Am. Acad. Dermatol. 2025, 92, 1394–1395. [Google Scholar] [CrossRef] [PubMed]
  52. Brink, M.; Huisman, F.; Meeuwes, F.O.; van der Poel, M.W.M.; Kersten, M.J.; Wondergem, M.; Böhmer, L.; Woei-A-Jin, F.J.S.H.; Visser, O.; Oostvogels, R.; et al. Treatment strategies and outcome in relapsed peripheral T-cell lymphoma: Results from the Netherlands Cancer Registry. Blood Adv. 2024, 8, 3619–3628. [Google Scholar] [CrossRef] [PubMed]
  53. Moskowitz, A.; Ganesan, N.; Chang, T.; Davey, T.; Hancock, H.; Smith, M.; Assini, A.; Sarmasti, L.; Miller, T.; Gibaldi, A.; et al. Dual-Targeted Therapy with Ruxolitinib Plus Duvelisib for T-Cell Lymphoma. Blood 2024, 144, 463. [Google Scholar] [CrossRef]
  54. Vahabi, S.M.; Bahramian, S.; Esmaeili, F.; Danaei, B.; Kalantari, Y.; Fazeli, P.; Sadeghi, S.; Hajizadeh, N.; Assaf, C.; Etesami, I. JAK Inhibitors in Cutaneous T-Cell Lymphoma: Friend or Foe? A Systematic Review of the Published Literature. Cancers 2024, 16, 861. [Google Scholar] [CrossRef] [PubMed]
Table 1. Adverse effects of JAK inhibitors.
Table 1. Adverse effects of JAK inhibitors.
DrugAdverse Effects
RuxolitinibInfection, thrombocytopenia, anemia, neutropenia, bruising, dizziness, headache [38].
TofacitinibInfection, GI perforation, rheumatoid and psoriatic arthritis, ulcerative colitis, anemia, neutropenia, elevated liver enzymes, elevated lipids, lymphoproliferative disorders [39].
GolidocitinibInfection, thrombocytopenia, anemia, neutropenia, hypertriglyceridemia, hyperuricemia, elevated liver enzymes, pyrexia [31].
CerdulatinibInfection, anemia, neutropenia, elevated lipase and amylase, fatigue [33].
UpadacitinibInfection, GI perforation, anemia, neutropenia, hyperlipidemia, elevated liver enzymes, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, ulcerative colitis [40].
AbrocitinibInfection, cardiovascular events, thrombosis, thrombocytopenia, lymphopenia, lymphoma, lung cancer [41].
Table 2. Clinical trials of JAK inhibitors for T-cell lymphomas.
Table 2. Clinical trials of JAK inhibitors for T-cell lymphomas.
ClinicalTrials.gov IDDrugDiseasePhaseAnticipated Completion Date
NCT05010005Ruxolitinib
Duvelisib		R/R T or NK cell lymphomaIAugust 2027
NCT02974647RuxolitinibR/R T or NK cell lymphomaIINovember 2025
NCT07283822Ruxolitinib
Pembrolizumab		R/R T-cell lymphomaIIJanuary 2029
NCT07278856Ruxolitinib
CHOP		Newly diagnosed nodal T-follicular helper cell lymphomaI31 March 2027
NCT05745714Ruxolitinib
Venetoclax
Dexamethasone
Cyclophosphamide
Cytarabine		R/R precursor T-lymphoblastic lymphoma/leukemiaI/II2 February 2032
NCT06698822Tofacitinib (Topical)CTCLII19 October 2026
NCT07279584GolidocitinibR/R PTCLII31 December 2027
NCT07032532GolidocitinibNewly diagnosed PTCLIIDecember 2028
NCT06757387Golidocitinib
Chidamide		R/R PTCLI/II30 December 2030
NCT07209163Golidocitinib
Linperlisib
Tazemetostat		R/R PTCLI/IIMarch 2027
NCT06739265Golidocitinib
CHOP		Newly diagnosed PTCLI/II1 September 2026
NCT05963347Golidocitinib
CHOP		Newly diagnosed PTCLII31 July 2026
NCT06733051Golidocitinib
Benmelstobart		R/R extranodal NK/T-cell lymphomaIIDecember 2028
NCT07093710Golidocitinib
Mitoxantrone
GemOx		R/R PTCLI/II1 August 2029
NCT06630091Golidocitinib
CHOP		Newly diagnosed PTCLII5 July 2029
NCT07234162Golidocitinib
Chidamide
Pralatrexate
Gemcitabine
Belinostat		R/R PTCLIII31 October 2028
NCT06701344Golidocitinib
CHOP		Intestinal T-cell lymphomaII4 December 2027
NCT07081607Golidocitinib
Azacitadine
Chimamide		PTCLII16 July 2028
NCT06573138Golidocitinib
Anti PD-1 antibody
Selinexor		R/R NK/T-cell lymphomaII1 July 2027
NCT06966154Golidocitinib
Tislelizumab
Selinexor		R/R NK/T-cell lymphomaI/II30 May 2028
NCT07300514GolidocitinibPTCLIII30 December 2029
NCT06855823Golidocitinib
Pomalidomide		R/R PTCLI/IIDecember 2026
NCT04858256PacritinibR/R T-cell lymphomaIINovember 2028
NCT05900089IvarmacitinibR/R NK/T-cell lymphomaI1 June 2026
NCT06519526IvarmacitinibR/R PTCLII31 August 2027
CHOP: cyclophosphamide, doxorubicin, vincristine, and prednisone, CTCL: Cutaneous T-cell lymphoma, NK: Natural killer, PTCL: Peripheral T-cell lymphoma, R/R: Relapsed/refractory.
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Taza, G.; Ahmed, N.; Vaughn, J.L. JAK Inhibitors in the Treatment of T-Cell Lymphomas: Current Evidence and Future Directions. Cancers 2026, 18, 799. https://doi.org/10.3390/cancers18050799

AMA Style

Taza G, Ahmed N, Vaughn JL. JAK Inhibitors in the Treatment of T-Cell Lymphomas: Current Evidence and Future Directions. Cancers. 2026; 18(5):799. https://doi.org/10.3390/cancers18050799

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Taza, Gardenia, Naveed Ahmed, and John L. Vaughn. 2026. "JAK Inhibitors in the Treatment of T-Cell Lymphomas: Current Evidence and Future Directions" Cancers 18, no. 5: 799. https://doi.org/10.3390/cancers18050799

APA Style

Taza, G., Ahmed, N., & Vaughn, J. L. (2026). JAK Inhibitors in the Treatment of T-Cell Lymphomas: Current Evidence and Future Directions. Cancers, 18(5), 799. https://doi.org/10.3390/cancers18050799

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