Next Article in Journal
Generation of Stable Epithelial–Mesenchymal Hybrid Cancer Cells with Tumorigenic Potential
Previous Article in Journal
Identification and Validation of Potentially Clinically Relevant CpG Regions within the Class 2 Tumor Suppressor Gene SFRP1 in Pancreatic Cancer
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Cancers
Volume 15
Issue 3
10.3390/cancers15030682
cancers-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Efficacy and Safety of PD-1/PD-L1 Checkpoint Inhibitors versus Anti-PD-1/PD-L1 Combined with Other Therapies for Tumors: A Systematic Review

by
Yiru Zhang
1,2,
Qigu Yao
1,
Yong Pan
2,
Xinru Fang
1,
Haoying Xu
1,
Tingxiao Zhao
1,2,
Guangqi Zhu
2,
Tianan Jiang
3,4,
Shibo Li
2,* and
Hongcui Cao
1,5,*
1
State Key Laboratory for the Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, 79 Qingchun Rd., Hangzhou 310003, China
2
Department of Infectious Disease, Zhoushan Hospital, Wenzhou Medical University, 739 Dingshen Rd., Zhoushan 316021, China
3
Department of Ultrasound Medicine, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China
4
Key Laboratory of Pulsed Power Translational Medicine of Zhejiang Province, 79 Qingchun Rd., Hangzhou 310003, China
5
Key Laboratory of Diagnosis and Treatment of Aging and Physic-Chemical Injury Diseases of Zhejiang Province, 79 Qingchun Rd., Hangzhou 310003, China
*
Authors to whom correspondence should be addressed.
Cancers 2023, 15(3), 682; https://doi.org/10.3390/cancers15030682
Submission received: 25 November 2022 / Revised: 29 December 2022 / Accepted: 18 January 2023 / Published: 22 January 2023
(This article belongs to the Topic Advances in Anti-Cancer Drugs)
Browse Figures
Versions Notes

Abstract

:

Simple Summary

There is a wide range of choices for combining PD-1/PD-L1 checkpoint inhibitors with other measures in treating tumors, but certain choices of regimens are still controversial. We aimed to investigate the therapeutic efficacy and potential side effects of combination therapy with anti-PD-1/PD-L1 compared to anti-PD-1/PD-L1 monotherapy. Meanwhile, we also explored whether different combination strategies would yield consistent efficacy across different types of tumors. Our study can provide important and useful information for clinicians and encourage the enrollment of more clinical trials for anti-PD-1/PD-L1 combination therapy.

Abstract

Objective: In recent years, the anti-programmed cell death protein-1 and its ligand (PD-1/PD-L1) or combination therapies have been recommended as an alternative emerging choice of treatment for oncology patients. However, the efficacy and adverse events of different combination strategies for the treatment of tumors remain controversial. Methods: PubMed, Embase, Cochrane Library, the American Society of Clinical Oncology (ASCO), and the European Society of Medicine Oncology (ESMO) were searched from database inception until 16 February 2022. The endpoints of objective response rate (ORR), disease control rate (DCR), overall survival (OS), progression-free survival (PFS), and adverse events (AEs) were analyzed from different treatment schemes and tumor types. The protocol was registered in PROSPERO (CRD42022328927). Results: This meta-analysis included forty-eight eligible studies. Combination therapy has improved ORR (RR = 1.40, p < 0.001), DCR (RR = 1.22, p < 0.001), and PFS (the median survival ratio (MSR) was estimated to be 1.475 p < 0.001) compared to anti-PD-1/PD-L1 but had no significant benefit on OS (MSR was estimated to be 1.086 p = 0.117). Besides, combination treatment strategies are more toxic in any grade AEs (RR = 1.13, p < 0.001) and grade 3–5 AEs (RR = 1.81, p < 0.001). Conclusions: Treatment with PD-1/PD-L1 inhibitors in combination with other antitumor therapies improve patients’ ORR, DCR, and PFS compared to anti-PD-1/PD-L1. However, it is regrettable that there is no benefit to OS and an increased risk of AEs in combinatorial therapies.

1. Introduction

In the new global economy, tumors have become a central issue for health. Data from a study suggest that there are approximately 19.3 million new cancer cases and 10.0 million cancer deaths in 2020 worldwide, projected to grow by more than 47% in 2040, which poses a serious threat to the quality of human life [1]. Consequently, how to choose an anti-cancer regimen has long been a question of great interest in a wide range of fields. From the discovery of the cytotoxic T lymphocyte-associated protein 4 (CTLA-4) in the 1980s to the programmed cell death protein 1 (PD-1) in the 1990s [2], immunotherapy has shown promising potential in various malignancies [3]. This shows a need to be explicit about exactly what is meant by the word PD-1. PD-1 is an immune checkpoint receptor in the tumor microenvironment (TME) [4], which is expressed on activated T cells, B cells, and natural killer cells [5]. When binding with the ligand PD-L1 or PD-L2, two motifs of PD-1 were phosphorylated, ending in the suppression of T cell proliferation and response. Therefore, blocking PD-1/PD-L1 with antibodies can strengthen pre-existent antitumor immune activity, which provides patients with a durable anti-tumor immune response [5]. Since the approval of ipilimumab in 2011, immune checkpoint inhibitors (ICIs) have been attracting a lot of interest, and seven of them for the PD-1/PD-L1 pathway have been approved by the FDA (U.S. Food and Drug Administration) so far [6]. This emerging immunomodulatory pathway was recognized by the 2018 Nobel Prize in Medicine and Physiology, which has revolutionized the traditional therapeutic approach to cancer and offers numerous options for cancer treatment [7].
Although this drug is promising, one study reported that one-third of patients had relapsed due to drug resistance [8]. Sharma has discussed the mechanisms of drug resistance, providing the theoretical basis for the combination therapy of PD-1/PD-L1 inhibitors with other treatment strategies to overcome drug resistance [9]. This is why most new trials have been combinatorial therapies since 2014, which to overcome drug resistance associated with monotherapy [10]. For example, one study by Wei examined the trend in anti-PD-1 and anti-CTLA4 combination strategies with favorable outcomes compared to monotherapy [11]. As of December 2021, 5683 clinical trials are assessing the effectiveness of anti-PD-1/PD-L1, with combination therapies leading the way (83%) and monotherapy continuing to decline (17%) [10]. However, a broad-scale study by Boyer reached different conclusions, finding that response rates remain modest for pembrolizumab plus ipilimumab [12]. It is therefore questionable whether different combination strategies and different tumor types produce consistent efficacy. Another point is that monotherapy is usually well-tolerated [13], but does the value of the efficacy brought by the current crowd-promoted combination therapy fail to balance the corresponding adverse effects in most studies? To date, these problems have received scant attention in the current meta-analysis.
Our group has previously explored the efficacy of PD-1/PD-L1 inhibitors plus other therapeutic regimens versus other therapeutic regimens and found the combination to be superior [14]. To further explore, we conducted a meta-analysis of eligible clinical trials to assess the efficacy and safety of single-agent anti-PD-1/PD-L1 versus anti-PD-1/PD-L1 combination therapy in order to provide clinical guidance on the choice of treatment options for patients with different tumors.

2. Materials and Methods

2.1. Search Strategy

We systematically scanned the associated literature published from the inception of the database to 16 February 2022 via a search of PubMed, Embase, and the Cochrane Library. There were no restrictions on region, age, gender, follow-up time, or tumor type. Combined with the retrieval strategy of Medical Subject Headings (MeSH) terms and free text words, we searched for a combination of the following terms: “PD-1”, “PD-L1”, and “tumor”. The specific search form used in PubMed can be downloaded in Supplementary Table S1. In addition to this, we have browsed American Society of Clinical Oncology (ASCO), clinicaltrials.gov, and European Society of Medicine Oncology (ESMO) for related resources that may be useful.

2.2. Selection Criteria

Studies were considered if they met the inclusion criteria as follows: (a) prospective clinical studies and the clinical registration number is available; (b) patients diagnosed with tumor received a combination of PD-1/PD-L1 inhibitors and other therapies (immunotherapy, targeted therapy, radiotherapy, chemotherapy, and other immune regulatory factors) in the experimental group, while treated with anti-PD-1/PD-L1 in the control group; (c) studies reported any of the following endpoints: objective response rate (ORR), disease control rate (DCR), overall survival (OS), progression-free survival (PFS), and adverse events (AEs).
The following studies have been excluded to minimize the risk of bias: (a) not in English; (b) editorials, comments, and case reports; (c) basic experiments; (d) multiple articles that analyzed the same trials.

2.3. Data Extraction Quality Assessment

Data were extracted independently by two researchers (Y. Zhang and Q. Yao) whose disagreements would be settled to reach a majority decision by a third investigator (H. Cao). The following information was picked up from forty-eight studies: first author, publication year, study phase, tumor type, sample size, interventions, PubMed Unique Identifier (PMID), registration number, median follow-up, median age, region, gender, primary results (containing ORR, DCR, median overall survival (mOS), the hazard ratio of OS, median progression-free survival (mPFS), the hazard ratio of PFS), and secondary AEs events (involving any-grade AEs and grade 3–5 AEs). This meta-analysis is composed according to the guidance of Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020.

2.4. Statistical Analysis

The risk ratio (RR) of ORR, DCR, and AEs and the hazard ratio (HR) of OS and PFS were calculated using Review Manager 5.4 (https://training.cochrane.org/, accessed on 16 April 2022). Due to the small number of articles providing HR directly, we also computed summary estimates for mOS and mPFS using Stata Statistical Software 16 (Stata Corp., College Station, TX, USA). In addition to the subgroup analysis of different tumor types and treatment schemes, we also used Cochran’s Q chi-square test and I2 statistics to evaluate the heterogeneity across studies (p < 0.1 and I2 > 50% were considered highly heterogeneous and a random-effects model was chosen, and vice versa for a fixed-effects model). Begg’s, Egger’s, and Harbord’s tests were used when necessary to assess publication bias, with significance set at p < 0.1. All statistical tests were two-sided, with p < 0.05 being regarded as significant.

3. Results

3.1. Eligible Studies and Quality

Through our retrieval strategy, 80,099 articles were finally retrieved from the database. After deleting duplicates, browsing titles and abstracts, and reviewing the full text, a total of 48 eligible clinical controlled trials involving 11,385 patients were included in the meta-analysis. The detailed literature screening and selection process is illustrated in Figure 1. Furthermore, the Cochrane Collaboration tool was applied to assess the quality of the included RCT studies. The results of each project evaluated were classified as high-risk, low-risk, or unclear (Supplementary Figures S1 and S2).

3.2. Study Characteristics

The results demonstrate the basic characteristics of qualified research established from the database in Table 1 and Supplementary Table S2. Five treatments were covered in 48 studies, involving 26 PD-1/PD-L1 + immunotherapy vs. PD-1/PD-L1, 8 PD-1/PD-L1 + targeted therapy vs. PD-1/PD-L1, 8 PD-1/PD-L1 + chemotherapy vs. PD-1/PD-L1, 4 PD-1/PD-L1 + radiotherapy vs. PD-1/PD-L1 and 2 PD-1/PD-L1 + other drugs vs. PD-1/PD-L1. In addition, to make the results more clinically significant, we also diversified the analysis of the efficacy from the perspective of tumor type. Among the forty-eight studies, the vast majority of tumor types included digestive system tumors (n = 11), genitourinary system tumors (n = 8), non-small cell lung cancer (n = 8), head and neck squamous cell carcinoma (n = 7), and melanoma (n = 6). The remaining solid tumors were glioblastoma (n = 2), nasopharyngeal carcinoma (n = 1, including other pathological types such as undifferentiated in addition to squamous cell carcinoma), small cell lung cancer (n = 1), malignant pleural mesothelioma (n = 1), metastatic sarcoma (n = 1), and multiple tumor types (n =1), as well as Hodgkin’s lymphoma (n = 1), among hematologic system tumors.

3.3. Objective Response Rate (ORR)

The objective response rate is defined as the proportion of patients whose tumor volume shrinks to a pre-specified value and can maintain the minimum time requirement, as the sum of the proportion with complete and partial response. According to the treatment protocol, 41 of 48 studies provided direct or indirect access to ORR data. Heterogeneity tests showed greater heterogeneity in the included studies (p < 0.001, I2 = 74%), and effect sizes were combined using a random-effects model. In Figure 2, the results indicate that RR = 1.40, 95% CI (1.22, 1.59), and the difference in ORR was statistically significant in the experimental group compared to the control group (p < 0.001). PD-1/PD-L1 combined with chemotherapy and immunotherapy improved response rates of cancer clinical treatment as evidenced in subgroup analysis. In the subgroup analysis based on specific tumor types (Supplementary Figure S3), ORR was better in the combination group for NSCLC (p = 0.01), SCLC (p = 0.03), genitourinary tumors (p < 0.001), digestive tumors (p < 0.001), and nasopharyngeal carcinoma (p < 0.001). Among them, nasopharyngeal carcinoma and digestive tumors gained more clinical benefits, with RR = 2.67, 95% CI (1.95, 3.66) and RR = 2.41, 95% CI (1.68, 3.46), respectively.

3.4. Disease Control Rate (DCR)

Disease control rate was characterized as the proportion of patients with complete response, partial response, and stable disease among all patients. DCR was reported in 34 studies (Figure 3). Heterogeneity test: p < 0.001, I2 = 74%. The meta-analysis demonstrated RR = 1.22, 95% CI (1.12, 1.34), with a statistically considerable difference in the combination arm as compared to the mono-drug group (p < 0.001). Among the five different combination regimens, those with improved remission rates were chemotherapy [RR = 1.56, 95% CI (1.36, 1.78), p < 0.001], radiotherapy [RR = 1.41, 95% CI (1.04, 1.91), p = 0.03], and targeted therapy [RR = 1.15, 95% CI (1.02, 1.30), p = 0.03]. Similarly, as seen in the forest plot in Supplementary Figure S4, nasopharyngeal cancer [RR = 1.65, 95% CI (1.38, 1.98), p < 0.001], genitourinary tumors [RR = 1.35, 95% CI (1.11, 1.64), p = 0.002], and digestive system tumors [RR = 1.30, 95% CI (1.06, 1.59), p = 0.01] achieved varying degrees of benefit.

3.5. Overall Survival (OS)

Overall survival was defined as the time from when the patient received treatment to the time of death from any cause or the cut-off time for follow-up. Of all the included studies, 11 articles directly provided a hazard ratio for OS. As illustrated in Figure 4 and Supplementary Figure S5, no improvement in OS in the experimental group was seen compared to the control arm (p = 0.64), whether analyzed by treatment or by the tumor as a subgroup.
Since the number of studies with directly available HR was not large, we further extracted the median overall survival of the articles and combined their effect sizes for a more comprehensive analysis of OS (Table 2 and Supplementary Table S3). On the basis of this analysis of overall survival time, in which there was significant heterogeneity (I2 = Please use the update Figure 4.95.2%), the median survival ratio (MSR) was estimated to be 1.086 (p = 0.117), indicating that the median survival time of the intervention group was 1.086 times that of the control group, and the difference was not found to be statistically significant as well. Subgroups were analyzed for differences between groups for different treatment schedules and tumor types, respectively, and their results revealed that (a) there were no statistically significant differences between the experimental group compared with the control arm for different combination regimens (p = 0.343), and (b) there was a statistically significant difference among the different tumor types in the combination group compared to anti-PD-1/PD-L1 (p < 0.001). Surprisingly, adding another drug to the treatment strategy does not appear to result in longer overall survival for tumor patients compared to anti-PD-1/PD-L1.

3.6. Progression-Free Survival (PFS)

Progression-free survival was defined as the time to tumor progression or follow-up endpoint after treatment. The hazard ratio of PFS was available in 13 studies. The subgroup analyses are summarized in Supplementary Figures S6 and S7. When the 13 studies were grouped by therapeutic schedules or tumor types, our meta-analysis showed that no statistically significant amelioration in PFS was observed in all groups except genitourinary tumors compared to the control group; in other words, there was no statistically significant difference between the intervention and control groups (p = 0.15).
Consequently, the same was applied to make full use of the data on the median progression-free survival (Table 3 and Supplementary Table S4). The number of included studies by treatment and by tumor was 38 and 37 respectively. The two numbers are different because one article describing various solid tumors did not provide a tumor-specific median PFS when classified by the tumor. As seen in both tables, there was obvious heterogeneity in the study (I2 =97.5%). In the treatment scheme, the MSR was estimated to be 1.475 (p < 0.001), while it was estimated to be 1.473 (p < 0.001) in the tumor type. The corresponding findings of this meta-analysis demonstrated that the median survival time of the intervention group was 1.475 times and 1.473 times longer than in the control arm, and there tended to be a statistical difference between the two groups as well (p < 0.05). It suggested that although there was no statistical difference in the risk ratio of PFS, the MSR of median progression-free survival in the experimental group was superior to that in the control group.

3.7. Incidence of All-Grade and Grade 3–5 Adverse Events (AEs)

A total of 48 studies with 5993 patients in the experimental groups and 5507 patients in the PD-1/PD-L1 inhibitors arm were included, and the occurrence of all-grade and grade 3–5 AEs were analyzed. Because different studies focus on a variety of AEs, we merged and selected several events with a large number of reports to analyze (Table 4 and Table 5). An analysis of the results showed that the 22 selected all-grade AEs were statistically significant in the experimental group in comparison to the control group (p < 0.05). However, among the six corresponding grade 3–5 AEs, RR was not statistically different (pruritus, thyroid abnormalities, pain, hypothyroidism, constipation, infection). Patients receiving combination therapy were at an increased risk of developing any grade AEs [RR = 1.13, 95% CI (1.08–1.18), p < 0.001] and high-grade AEs [RR = 1.81, 95% CI (1.63–2.01), p < 0.001] versus the monotherapy group. In our included studies, the first three most common all-grade and grade 3–5 adverse reactions were the same, all in the order of fatigue (RR = 1.31 and 1.93), diarrhea (RR = 1.87 and 3.35), and rash (RR = 1.81 and 2.07). The highest risk-averse events were both reduced platelet count, with [RR = 2.83, 95%CI (1.27, 6.29)] and [RR = 6.12, 95%CI (1.86, 20.16)] for all-grade and grade 3–5 AEs, respectively.

3.8. Publication Bias

Both Begg’s test and Egger’s test showed that the included studies had no significant publication bias (p > 0.1) in all the outcome indicators, and the Galbraith diagram (p > 0.1) was also drawn in ORR and DCR (Supplementary Figures S8–S11).

4. Discussion

With the rapid development of oncology and immunology, tumor immunotherapy has made major progress and has become another important pillar of anti-tumor treatments apart from surgery, radiotherapy, and chemotherapy, changing the therapeutic pattern of many tumors. For example, the previous treatment agent for liver cancers mainly constitutes targeted drugs and chemoradiotherapy drugs, supplemented by symptomatic drugs [62]. Now, the clinical trials of PD-1/PD-L1 inhibitors are widely carried out in various solid tumors and have been recommended for early use.
Collectively, the 48 studies in this meta-analysis outline a critical role in the efficacy and safety of PD-1/PD-L1 inhibitors in tumors. Based on the available clinical trials, which were reviewed and summarized as comprehensively as possible, there are two basic taxonomies currently being adopted in research into them in this study. One is the treatment scheme, and the other is the tumor type. The vast majority of patients experienced adverse events to varying degrees, with fatigue being particularly common. Both regimens had their pros and cons, with combination therapy showing superiority over monotherapy in ORR, DCR, and PFS, while monotherapy was superior to combination in AE. Neither was clinically significant in OS. Taken together, when making clinical treatment decisions for patients with different tumors, it may be preferable to conservatively recommend combinatorial therapies to improve patient prognosis while also considering patient tolerance to adverse effects.
The four major endpoints of oncology treatment include ORR, DCR, OS, and PFS, with the first two reflecting the near-term efficacy and the last two being the long-term efficacy indicators. The near-term efficacy indicators mainly assess the direct impact of drugs on tumors, with ORR being the most critical, while the long-term efficacy indicators mainly assess the effects of drugs on patients’ survival time, with OS being the most reliable clinical trial endpoint for evaluating antineoplastic drugs so far [63]. Therefore, we have endeavored to extract and analyze the possible clinical benefits of these four indicators for applications. A comparison of the findings with the study reported elsewhere confirms combination therapy showed numerically higher ORR [64] compared with monotherapy, but not improved OS significantly [65]. In contrast to these earlier findings, however, no evidence of the benefit of PFS was detected in this meta-analysis. The reason for this discrepancy may be attributed to the small number of studies included in this meta-analysis that directly provided the HR of OS and PFS. Since the statistical values of ORR, DCR, and PFS in the combined treatment group were improved than those of the control group, the mortality was also higher due to the higher AE. Moreover, our meta-analysis shows that compared with the control group, the combined treatment group has no advantage in OS HR. But the efficacy of clinical trials is also affected by many factors, such as accessibility and financial burden. Therefore, we propose the following solutions. First of all, symptomatic treatment of AE and prevention of 3–5 levels of AE should be carried out to reduce the death rate caused by AE. Second, more clinical studies and design trials should be included to reduce the impact of other non-research factors.
Therefore, to make the findings more convincing, we also considered median survival as a combined effect size and calculated a median survival ratio point estimate as a further argument for the above speculation. One unanticipated finding was that these results indeed further support the benefit of PFS. These findings are consistent with that of Yang (2020) [66], who also has demonstrated that combination therapy significantly improved ORR and DCR and prolonged mPFS but has not yet impacted overall survival. Inspired by the conjecture presented in the previous article, we venture to speculate that the activity of combination therapy for tumors may be more of a cumulative effect than a synergistic one.
Based on the subgroup analysis of tumor types, the overall efficacy evaluation of long- and short-term efficacy for different cancer types in combination therapy and monotherapy showed consistency with the treatment regimens. The most obvious finding to emerge from the analysis is that compared with the single-drug group, ORR, DCR, and PFS of the digestive system and genitourinary system tumors in the combined treatment group represent better clinical advantages. We observed that these two tumor types accounted for a higher percentage of the included studies. Therefore, based on these data, we infer that this result may be due to the number of studies. To go a step further, a large proportion of studies with small sample sizes are more prone to findings that contradict the conclusions drawn from the results of the combined effects. Recent systematic literature reviews concluded that the superiority of combined anti-CTLA-4 and anti-PD-1 therapy for melanoma and NSCLC in the response rates or OS has been proven to date, which is contrary to our conclusion (p = 0.32 and p = 0.1) [67,68]. In recent years, clinical studies on reversing drug resistance to anti-PD-1 by modulating intestinal flora are in full swing. In one well-known recent experiment, Baruch et al. found a significant increase in the number of immune cell infiltration in melanoma patients who had undergone fecal transplantation, successfully activating the immune response in the patients [69]. Previously, Janney et al. described various possible mechanisms by which intestinal flora affects the treatment of colorectal cancer, suggesting that modulating intestinal flora to overcome immunotherapy resistance may be another viable avenue [70]. Therefore, the other speculation is that combination therapy may be more advantageous in digestive system tumors than in tumors of other systemic origins.
The National Cancer Institute (NCI) provides a grading (severity) scale for each AE term, which allows recognition of relevant clinical manifestations for the early assessment of toxic reactions. Comparison of the findings with those of other studies [13,71,72,73,74,75] confirms that patients with combination therapy are more likely to experience AEs than those in the anti-PD-1/PD-L1 arm. The higher risk of various adverse reactions comes from the digestive system and the hematological system, suggesting that front-line clinical workers are expected to be aware at an early stage and take preventive measures as soon as possible. A recent meta-analysis mentioned that anti-PD-L1 therapy can achieve long-term tumor control by maintaining immune activation [76]. However, excessive immune activation can induce immune-related adverse events (irAE). ICIs may contribute to the development of irAEs by affecting peripheral tolerance to autoantigens, leading to the formation of autoantibodies. The association between the development of immune-related adverse events and improvement in disease prognosis are two sides of the same coin. The occurrence of irAE can be treated with supportive measures such as steroids and other immunosuppressive agents without discontinuation of ICI therapy. Therefore, early diagnoses of irAE, symptom monitoring, and patient education can prevent the exacerbation of AE to higher levels of toxicity.
This study adds to the growing body of research that indicates the response rates and survival of the various combination strategies are not consistently better than those of anti-PD-1/PD-L1. In addition, the efficacy of different types of tumors depends on the specific treatment regimen. Although various similar treatment therapies and tumors can be cross-referenced, specific problems should be analyzed, and no generalization should be made. Thirdly, as to the question of how to balance efficacy and adverse effects, the recommendation of this meta-analysis is that the more potent strategy is advised to improve patient prognosis without compromising patient life and quality of life. Last but not least, given that the combination of nivolumab and ipilimumab is not a cost-effective option compared to nivolumab therapy [77], patients’ financial burdens should also be taken into account when choosing an option.
It is reported that high monocyte count is a poor prognostic factor for patients with solid tumors [78,79]. The prognosis of colorectal cancer and breast cancer patients with neutrophil to lymphocyte ratio >2.5 or increased neutrophil to lymphocyte ratio after surgery was significantly lower [80,81]. In the literature we included, we found that the density of CD8-positive tumor-infiltrating lymphocytes (CD8TIL) was higher, which could improve the prognosis of patients with oral cancer [16].
When anti-tumor drugs are combined, the order of administration is usually determined by the principles of cell dynamics, interaction, and stimulation. In the literature search, we found that the clinical trial of anti-PD-1/PD-L1 combination therapies did not give a clear order of administration. Anti-PD-1/PD-L1, as new anti-tumor drugs, their mechanism of action is different from that of traditional anti-tumor drugs. Due to the different understanding of the interaction between anti-PD-1/PD-L1 and traditional chemicals, there are many differences in the order of their combined use in clinical practice.
Inflammatory factor IFN-γ, inflammatory cells, such as T lymphocytes, can induce high expression of PD-L1, which is helpful in inhibiting tumors [82,83]. Based on the above literature, it is reasonable to speculate that the use of anti-inflammatory drugs can cooperate with PD-1/PD-L1 inhibitors to suppress the tumor immune escape and synergistically enhance the therapeutic effect of PD-1/PD-L1 inhibitors. Current mainstream combination strategies include immuno-oncology (IO) therapies, targeted therapies, chemotherapies, and radiotherapies. Based on the number of new trials started in recent years [84], emerging therapies of interest for the future may lie in combinations with approved therapies such as PARP inhibitors, as well as rising IO targets and agents such as TIGIT, TGFβ/TGFR, TLRs, oncolytic viruses, and cancer vaccines.
Admittedly, the scope of this study was limited in the following terms. First, of the 48 prospective clinical trials enrolled in this study, three were not randomized controlled trials and were not included in the risk of bias assessment. One included two single-arm phase 1 trials; another was a non-comparative phase 2 trial that included two independent trials; the other was a non-randomized controlled clinical phase 1 study. However, these studies meet our nadir criteria and have some implications for our research. Besides, some of the trials studied multiple similarly eligible cohorts simultaneously. We did not find differences by comparison, so the two cohorts with larger sample sizes were selected to reduce bias. Second, the sum of the total number of men and women in some studies did not match the number of interventions. We browsed and summarized the included literature and found that this was because the baseline data was filled in with the initial number of people, while the intervention number represented the number of available people, and people may have dropped out of the study in the middle of the trial so that the numbers were not exactly the same. Third, this meta-analysis did not standardize tumor and adverse effect evaluation criteria. Although there were differences, most studies used RECIST version 1.1 and CTCAE version 4.0. Fourth, a majority of the included studies failed to explore patients with PD-1/PD-L1 expression greater than 50% and less than 50%. Previous research has established that the response rate for patients with PD-L1 TPS of ≥50% was found to be 45.2%, compared to 16.5% and 10.7% among patients with a TPS of 1–49% and <1%, respectively [85]. Although there are no available prospective data on the efficacy of ICI monotherapy versus ICI plus chemotherapy in patients with low tumor PD-L1 expression levels (TPS of <50%), it is suggested that more upcoming clinical trials could be conducted to discuss the efficacy separately according to the expression of PD-1/PD-L1 [86]. Finally, most of our analyses fell into the category of no or mild to moderate heterogeneity (I2 ≤ 75%) and used a more conservative random effects model. In addition, for treatments with greater heterogeneity (I2 > 75%), we performed a subgroup analysis (i.e., by tumor type and treatment regimen). Eventually, high heterogeneity was found in the ORR of anti-PD-1/PD-L1 plus chemotherapy, DCR of the genitourinary system, HNSCC, melanoma, and PFS of anti-PD-1/PD-L1 plus targeted agents. The heterogeneity may be due to the fact that the number of articles eligible for inclusion is not very large.

5. Conclusions

The most obvious finding to emerge from this study is that PD-1/PD-L1 inhibitors combined with chemotherapy and immunotherapy improve ORR, and those with improved DCR were chemotherapy, radiotherapy, and targeted therapy. ORR was better in the combination group for NSCLC, SCLC, genitourinary tumors, digestive tumors, and nasopharyngeal carcinoma, while nasopharyngeal cancer, genitourinary tumors, and digestive system tumors perform better in DCR. PFS in the experimental group was superior to that in the control group. However, the addition of another drug to the treatment strategy does not appear to result in prolonged OS in tumor patients compared to anti-PD-1/PD-L1. In addition, all-grade and grade 3–5 AEs were greater in the experimental group compared to the control group.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/cancers15030682/s1, Figure S1: Risk of bias graph: covers 45 studies on the risk of bias judgments, Table S1: Search strategy, Figure S2: Risk of bias summary: covers 45 studies on the risk of bias judgments, Table S2: Baseline demographics and clinical characteristics, Figure S3: Forest Plot of the Risk ratio of ORR based on tumor types: anti-PD-1/PD-L1 versus combination therapy (digestive system tumors, genitourinary system tumors, non-small cell lung cancer, head and neck squamous cell carcinoma, melanoma, glioblastoma, small cell lung cancer, malignant pleural mesothelioma, nasopharyngeal carcinoma, and classic Hodgkin’s lymphoma), Table S3: Median survival ratio of OS based on tumor types, Figure S4: Forest Plot of the Risk ratio of DCR based on tumor types: anti-PD-1/PD-L1 versus combination therapy (digestive system tumors, genitourinary system tumors, non-small cell lung cancer, head and neck squamous cell carcinoma, melanoma, glioblastoma, small cell lung cancer, malignant pleural mesothelioma, and nasopharyngeal carcinoma), Table S4: Median survival ratio of PFS based on tumor types, Figure S5: Forest Plot of the Hazard ratio of OS based on tumor types: anti-PD-1/PD-L1 versus combination therapy (genitourinary system tumors, non-small cell lung cancer, head and neck squamous cell carcinoma, and melanoma), Figure S6: Forest Plot of the Hazard ratio of PFS based on therapeutic schedules: anti-PD-1/PD-L1 versus combination therapy (immunotherapy, targeted therapy, radiotherapy, chemotherapy, and other drugs), Figure S7: Forest Plot of the Hazard ratio of PFS based on tumor types: anti-PD-1/PD-L1 versus combination therapy (digestive system tumors, genitourinary system tumors, non-small cell lung cancer, head and neck squamous cell carcinoma, and melanoma), Figure S8: Begg’s test (P=0.406), Egger’s test (P=0.931), and Harbord’s test (P=0.952) showed no significant publication bias in ORR, Figure S9: Begg’s test (P=0.448), Egger’s test (P=0.554), and Harbord’s test (P=0.348) showed no significant publication bias in DCR, Figure S10: Begg’s test and Egger’s test (A)Begg’s test (P=0.533) and Egger’s test (P=0.735) showed no significant publication bias in Hazard ratio of OS (B)Begg’s test (P=0.669) and Egger’s test (P=0.383) showed no significant publication bias in Hazard ratio of PFS, Figure S11: Begg’s test and Egger’s test (A)Begg’s test (P=0.803) and Egger’s test (P=0.860) showed no significant publication bias in median OS (B)Begg’s test (P=0.204) and Egger’s test (P=0.952) showed no significant publication bias in median PFS.

Author Contributions

H.C., Y.Z. and Q.Y. contributed to the research conception and design. T.Z., G.Z. and Y.P. performed data analysis. Y.Z., Q.Y., X.F. and H.X. wrote the manuscript. H.C., T.J. and S.L. contributed to the review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the Key Research and Development Program of Zhejiang Province (No. 2023C03046), Zhejiang Province Major Science and Technology Project for Medicine and Health (No. WKJ-ZJ-2329), Development Project of National Major Scientific Research Instrument (No. 82027803), and Fundamental Research Funds for the Central Universities (No. 2022ZFJH003).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data generated or analyzed during this study are included in this article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

  1. Sung, H.; Ferlay, J.; Siegel, R.L.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J. Clin. 2021, 71, 209–249. [Google Scholar] [CrossRef] [PubMed]
  2. Couzin-Frankel, J. Breakthrough of the year 2013. Cancer immunotherapy. Science 2013, 342, 1432–1433. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Postow, M.A.; Callahan, M.K.; Wolchok, J.D. Immune Checkpoint Blockade in Cancer Therapy. J. Clin. Oncol. 2015, 33, 1974–1982. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Topalian, S.L.; Taube, J.M.; Pardoll, D.M. Neoadjuvant checkpoint blockade for cancer immunotherapy. Science 2020, 367, 6477. [Google Scholar] [CrossRef] [PubMed]
  5. Abril-Rodriguez, G.; Ribas, A. SnapShot: Immune Checkpoint Inhibitors. Cancer Cell 2017, 31, 848–848.e1. [Google Scholar] [CrossRef]
  6. Korman, A.J.; Garrett-Thomson, S.C.; Lonberg, N. The foundations of immune checkpoint blockade and the ipilimumab approval decennial. Nat. Rev. Drug Discov. 2021, 21, 509–528. [Google Scholar] [CrossRef]
  7. Wolchok, J. Putting the Immunologic Brakes on Cancer. Cell 2018, 175, 1452–1454. [Google Scholar] [CrossRef] [Green Version]
  8. Ribas, A.; Wolchok, J.D. Cancer immunotherapy using checkpoint blockade. Science 2018, 359, 1350–1355. [Google Scholar] [CrossRef] [Green Version]
  9. Sharma, P.; Hu-Lieskovan, S.; Wargo, J.A.; Ribas, A. Primary, Adaptive, and Acquired Resistance to Cancer Immunotherapy. Cell 2017, 168, 707–723. [Google Scholar] [CrossRef] [Green Version]
  10. Upadhaya, S.; Neftelinov, S.T.; Hodge, J.; Campbell, J. Challenges and opportunities in the PD1/PDL1 inhibitor clinical trial landscape. Nat. Rev. Drug Discov. 2022, 21, 482–483. [Google Scholar] [CrossRef]
  11. Wei, S.C.; Duffy, C.R.; Allison, J.P. Fundamental Mechanisms of Immune Checkpoint Blockade Therapy. Cancer Discov. 2018, 8, 1069–1086. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Boyer, M.; Şendur, M.A.N.; Rodríguez-Abreu, D.; Park, K.; Lee, D.H.; Çiçin, I.; Yumuk, P.F.; Orlandi, F.J.; Leal, T.A.; Molinier, O.; et al. Pembrolizumab Plus Ipilimumab or Placebo for Metastatic Non–Small-Cell Lung Cancer With PD-L1 Tumor Proportion Score ≥ 50%: Randomized, Double-Blind Phase III KEYNOTE-598 Study. J. Clin. Oncol. 2021, 39, 2327–2338. [Google Scholar] [CrossRef] [PubMed]
  13. Zhou, X.; Yao, Z.; Bai, H.; Duan, J.; Wang, Z.; Wang, X.; Zhang, X.; Xu, J.; Fei, K.; Zhang, Z.; et al. Treatment-related adverse events of PD-1 and PD-L1 inhibitor-based combination therapies in clinical trials: A systematic review and meta-analysis. Lancet Oncol. 2021, 22, 1265–1274. [Google Scholar] [CrossRef] [PubMed]
  14. Yao, Q.; Gu, L.; Su, R.; Chen, B.; Cao, H. Efficacy and safety of combination PD-1/PD-L1 checkpoint inhibitors for malignant solid tumours: A systematic review. J. Cell Mol. Med. 2020, 24, 13494–13506. [Google Scholar] [CrossRef] [PubMed]
  15. D’Angelo, S.P.; Mahoney, M.R.; Van Tine, B.A.; Atkins, J.; Milhem, M.M.; Jahagirdar, B.N.; Antonescu, C.R.; Horvath, E.; Tap, W.D.; Schwartz, G.K.; et al. Nivolumab with or without ipilimumab treatment for metastatic sarcoma (Alliance A091401): Two open-label, non-comparative, randomised, phase 2 trials. Lancet Oncol. 2018, 19, 416–426. [Google Scholar] [CrossRef]
  16. Ferrarotto, R.; Bell, D.; Rubin, M.L.; Hutcheson, K.A.; Johnson, J.M.; Goepfert, R.P.; Phan, J.; Elamin, Y.Y.; Torman, D.K.; Warneke, C.L.; et al. Impact of Neoadjuvant Durvalumab with or without Tremelimumab on CD8+ Tumor Lymphocyte Density, Safety, and Efficacy in Patients with Oropharynx Cancer: CIAO Trial Results. Clin. Cancer Res. 2020, 26, 3211–3219. [Google Scholar] [CrossRef] [Green Version]
  17. Ferris, R.; Haddad, R.; Even, C.; Tahara, M.; Dvorkin, M.; Ciuleanu, T.; Clement, P.; Mesia, R.; Kutukova, S.; Zholudeva, L.; et al. Durvalumab with or without tremelimumab in patients with recurrent or metastatic head and neck squamous cell carcinoma: EAGLE, a randomized, open-label phase III study. Ann. Oncol. 2020, 31, 942–950. [Google Scholar] [CrossRef]
  18. Gettinger, S.N.; Redman, M.W.; Bazhenova, L.; Hirsch, F.R.; Mack, P.C.; Schwartz, L.H.; Bradley, J.D.; Stinchcombe, T.E.; Leighl, N.B.; Ramalingam, S.S.; et al. Nivolumab Plus Ipilimumab vs Nivolumab for Previously Treated Patients With Stage IV Squamous Cell Lung Cancer: The Lung-MAP S1400I Phase 3 Randomized Clinical Trial. JAMA Oncol. 2021, 7, 1368. [Google Scholar] [CrossRef]
  19. Janjigian, Y.Y.; Bendell, J.; Calvo, E.; Kim, J.W.; Ascierto, P.A.; Sharma, P.; Ott, P.A.; Peltola, K.; Jaeger, D.; Evans, J.; et al. CheckMate-032 Study: Efficacy and Safety of Nivolumab and Nivolumab Plus Ipilimumab in Patients With Metastatic Esophagogastric Cancer. J. Clin. Oncol. 2018, 36, 2836–2844. [Google Scholar] [CrossRef]
  20. Kaseb, A.O.; Hasanov, E.; Cao, H.S.T.; Xiao, L.; Vauthey, J.-N.; Lee, S.S.; Yavuz, B.G.; Mohamed, Y.I.; Qayyum, A.; Jindal, S.; et al. Perioperative nivolumab monotherapy versus nivolumab plus ipilimumab in resectable hepatocellular carcinoma: A randomised, open-label, phase 2 trial. Lancet Gastroenterol. Hepatol. 2022, 7, 208–218. [Google Scholar] [CrossRef]
  21. Kelley, R.K.; Sangro, B.; Harris, W.; Ikeda, M.; Okusaka, T.; Kang, Y.-K.; Qin, S.; Tai, D.W.-M.; Lim, H.Y.; Yau, T.; et al. Safety, Efficacy, and Pharmacodynamics of Tremelimumab Plus Durvalumab for Patients With Unresectable Hepatocellular Carcinoma: Randomized Expansion of a Phase I/II Study. J. Clin. Oncol. 2021, 39, 2991–3001. [Google Scholar] [CrossRef] [PubMed]
  22. Kelly, R.J.; Lee, J.; Bang, Y.-J.; Almhanna, K.; Blum-Murphy, M.; Catenacci, D.V.; Chung, H.C.; Wainberg, Z.A.; Gibson, M.K.; Lee, K.-W.; et al. Safety and Efficacy of Durvalumab and Tremelimumab Alone or in Combination in Patients with Advanced Gastric and Gastroesophageal Junction Adenocarcinoma. Clin. Cancer Res. 2020, 26, 846–854. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Long, G.V.; Atkinson, V.; Lo, S.; Sandhu, S.; Guminski, A.D.; Brown, M.P.; Wilmott, J.S.; Edwards, J.; Gonzalez, M.; Scolyer, R.A.; et al. Combination nivolumab and ipilimumab or nivolumab alone in melanoma brain metastases: A multicentre randomised phase 2 study. Lancet Oncol. 2018, 19, 672–681. [Google Scholar] [CrossRef] [PubMed]
  24. Long, G.V.; Dummer, R.; Hamid, O.; Gajewski, T.F.; Caglevic, C.; Dalle, S.; Arance, A.; Carlino, M.S.; Grob, J.-J.; Kim, T.M.; et al. Epacadostat plus pembrolizumab versus placebo plus pembrolizumab in patients with unresectable or metastatic melanoma (ECHO-301/KEYNOTE-252): A phase 3, randomised, double-blind study. Lancet Oncol. 2019, 20, 1083–1097. [Google Scholar] [CrossRef] [PubMed]
  25. Omuro, A.; Vlahovic, G.; Lim, M.; Sahebjam, S.; Baehring, J.; Cloughesy, T.; Voloschin, A.; Ramkissoon, S.H.; Ligon, K.L.; Latek, R.; et al. Nivolumab with or without ipilimumab in patients with recurrent glioblastoma: Results from exploratory phase I cohorts of CheckMate 143. Neuro Oncol. 2018, 20, 674–686. [Google Scholar] [CrossRef] [Green Version]
  26. O’Reilly, E.M.; Oh, D.-Y.; Dhani, N.; Renouf, D.J.; Lee, M.A.; Sun, W.; Fisher, G.; Hezel, A.; Chang, S.-C.; Vlahovic, G.; et al. Durvalumab With or Without Tremelimumab for Patients With Metastatic Pancreatic Ductal Adenocarcinoma: A Phase 2 Randomized Clinical Trial. JAMA Oncol. 2019, 5, 1431–1438. [Google Scholar] [CrossRef] [PubMed]
  27. Paz-Ares, L.G.; Ramalingam, S.S.; Ciuleanu, T.-E.; Lee, J.-S.; Urban, L.; Caro, R.B.; Park, K.; Sakai, H.; Ohe, Y.; Nishio, M.; et al. First-Line Nivolumab Plus Ipilimumab in Advanced NSCLC: 4-Year Outcomes From the Randomized, Open-Label, Phase 3 CheckMate 227 Part 1 Trial. J. Thorac. Oncol. 2021, 17, 289–308. [Google Scholar] [CrossRef] [PubMed]
  28. Planchard, D.; Reinmuth, N.; Orlov, S.; Fischer, J.; Sugawara, S.; Mandziuk, S.; Marquez-Medina, D.; Novello, S.; Takeda, Y.; Soo, R.; et al. ARCTIC: Durvalumab with or without tremelimumab as third-line or later treatment of metastatic non-small-cell lung cancer. Ann. Oncol. 2020, 31, 609–618. [Google Scholar] [CrossRef] [Green Version]
  29. Powles, T.; van der Heijden, M.S.; Castellano, D.; Galsky, M.D.; Loriot, Y.; Petrylak, D.P.; Ogawa, O.; Park, S.H.; Lee, J.-L.; De Giorgi, U.; et al. Durvalumab alone and durvalumab plus tremelimumab versus chemotherapy in previously untreated patients with unresectable, locally advanced or metastatic urothelial carcinoma (DANUBE): A randomised, open-label, multicentre, phase 3 trial. Lancet Oncol. 2020, 21, 1574–1588. [Google Scholar] [CrossRef]
  30. Ready, N.E.; Ott, P.A.; Hellmann, M.D.; Zugazagoitia, J.; Hann, C.L.; de Braud, F.; Antonia, S.J.; Ascierto, P.A.; Moreno, V.; Atmaca, A.; et al. Nivolumab Monotherapy and Nivolumab Plus Ipilimumab in Recurrent Small Cell Lung Cancer: Results From the CheckMate 032 Randomized Cohort. J. Thorac. Oncol. 2020, 15, 426–435. [Google Scholar] [CrossRef]
  31. Scherpereel, A.; Mazieres, J.; Greillier, L.; Lantuejoul, S.; Dô, P.; Bylicki, O.; Monnet, I.; Corre, R.; Audigier-Valette, C.; Locatelli-Sanchez, M.; et al. Nivolumab or nivolumab plus ipilimumab in patients with relapsed malignant pleural mesothelioma (IFCT-1501 MAPS2): A multicentre, open-label, randomised, non-comparative, phase 2 trial. Lancet Oncol. 2019, 20, 239–253. [Google Scholar] [CrossRef] [PubMed]
  32. Schoenfeld, J.D.; Hanna, G.J.; Jo, V.Y.; Rawal, B.; Chen, Y.-H.; Catalano, P.S.; Lako, A.; Ciantra, Z.; Weirather, J.L.; Criscitiello, S.; et al. Neoadjuvant Nivolumab or Nivolumab Plus Ipilimumab in Untreated Oral Cavity Squamous Cell Carcinoma. A Phase 2 Open-Label Randomized Clinical Trial. JAMA Oncol. 2020, 6, 1563–1570. [Google Scholar] [CrossRef] [PubMed]
  33. Sharma, P.; Siefker-Radtke, A.; De Braud, F.; Basso, U.; Calvo, E.; Bono, P.; Morse, M.A.; Ascierto, P.A.; Lopez-Martin, J.; Brossart, P.; et al. Nivolumab Alone and With Ipilimumab in Previously Treated Metastatic Urothelial Carcinoma: CheckMate 032 Nivolumab 1 mg/kg Plus Ipilimumab 3 mg/kg Expansion Cohort Results. J. Clin. Oncol. 2019, 37, 1608–1616, Erratum in J. Clin. Oncol. 2019, 37, 2094. [Google Scholar] [CrossRef] [Green Version]
  34. Singh, A.S.; Hecht, J.R.; Rosen, L.; Wainberg, Z.A.; Wang, X.; Douek, M.; Hagopian, A.; Andes, R.; Sauer, L.; Brackert, S.R.; et al. A Randomized Phase II Study of Nivolumab Monotherapy or Nivolumab Combined with Ipilimumab in Patients with Advanced Gastrointestinal Stromal Tumors. Clin. Cancer Res. 2022, 28, 84–94. [Google Scholar] [CrossRef] [PubMed]
  35. Siu, L.L.; Even, C.; Mesía, R.; Remenar, E.; Daste, A.; Delord, J.-P.; Krauss, J.; Saba, N.F.; Nabell, L.; Ready, N.E.; et al. Safety and Efficacy of Durvalumab With or Without Tremelimumab in Patients With PD-L1-Low/Negative Recurrent or Metastatic HNSCC. The Phase 2 CONDOR Randomized Clinical Trial. JAMA Oncol. 2019, 5, 195–203. [Google Scholar] [CrossRef]
  36. Tawbi, H.A.; Schadendorf, D.; Lipson, E.J.; Ascierto, P.A.; Matamala, L.; Gutiérrez, E.C.; Rutkowski, P.; Gogas, H.J.; Lao, C.D.; De Menezes, J.J.; et al. Relatlimab and Nivolumab versus Nivolumab in Untreated Advanced Melanoma. New Engl. J. Med. 2022, 386, 24–34. [Google Scholar] [CrossRef]
  37. Wolchok, J.D.; Chiarion-Sileni, V.; Gonzalez, R.; Grob, J.-J.; Rutkowski, P.; Lao, C.D.; Cowey, C.L.; Schadendorf, D.; Wagstaff, J.; Dummer, R.; et al. Long-Term Outcomes With Nivolumab Plus Ipilimumab or Nivolumab Alone Versus Ipilimumab in Patients With Advanced Melanoma. J. Clin. Oncol. 2022, 40, 127–137. [Google Scholar] [CrossRef]
  38. Zamarin, D.; Burger, R.A.; Sill, M.W.; Powell, D.J., Jr.; Lankes, H.A.; Feldman, M.D.; Zivanovic, O.; Gunderson, C.; Ko, E.; Mathews, C.; et al. Randomized Phase II Trial of Nivolumab Versus Nivolumab and Ipilimumab for Recurrent or Persistent Ovarian Cancer: An NRG Oncology Study. J. Clin. Oncol. 2020, 38, 1814–1823. [Google Scholar] [CrossRef]
  39. Zimmer, L.; Livingstone, E.; Hassel, J.C.; Fluck, M.; Eigentler, T.; Loquai, C.; Haferkamp, S.; Gutzmer, R.; Meier, F.; Mohr, P.; et al. Adjuvant nivolumab plus ipilimumab or nivolumab monotherapy versus placebo in patients with resected stage IV melanoma with no evidence of disease (IMMUNED): A randomised, double-blind, placebo-controlled, phase 2 trial. Lancet 2020, 395, 1558–1568. [Google Scholar] [CrossRef]
  40. Eng, C.; Kim, T.W.; Bendell, J.; Argilés, G.; Tebbutt, N.C.; Di Bartolomeo, M.; Falcone, A.; Fakih, M.; Kozloff, M.; Segal, N.H.; et al. Atezolizumab with or without cobimetinib versus regorafenib in previously treated metastatic colorectal cancer (IMblaze370): A multicentre, open-label, phase 3, randomised, controlled trial. Lancet Oncol. 2019, 20, 849–861. [Google Scholar] [CrossRef]
  41. Gogas, H.; Dréno, B.; Larkin, J.; Demidov, L.; Stroyakovskiy, D.; Eroglu, Z.; Ferrucci, P.F.; Pigozzo, J.; Rutkowski, P.; Mackiewicz, J.; et al. Cobimetinib plus atezolizumab in BRAFV600 wild-type melanoma: Primary results from the randomized phase III IMspire170 study. Ann. Oncol. 2021, 32, 384–394. [Google Scholar] [CrossRef] [PubMed]
  42. Lee, M.S.; Ryoo, B.-Y.; Hsu, C.-H.; Numata, K.; Stein, S.; Verret, W.; Hack, S.P.; Spahn, J.; Liu, B.; Abdullah, H.; et al. Atezolizumab with or without bevacizumab in unresectable hepatocellular carcinoma (GO30140): An open-label, multicentre, phase 1b study. Lancet Oncol. 2020, 21, 808–820. [Google Scholar] [CrossRef] [PubMed]
  43. McDermott, D.F.; Huseni, M.A.; Atkins, M.B.; Motzer, R.J.; Rini, B.I.; Escudier, B.; Fong, L.; Joseph, R.W.; Pal, S.K.; Reeves, J.A.; et al. Clinical activity and molecular correlates of response to atezolizumab alone or in combination with bevacizumab versus sunitinib in renal cell carcinoma. Nat. Med. 2018, 24, 749–757. [Google Scholar] [CrossRef] [PubMed]
  44. Nayak, L.; Molinaro, A.M.; Peters, K.B.; Clarke, J.L.; Jordan, J.T.; de Groot, J.F.; Nghiemphu, P.L.; Kaley, T.J.; Colman, H.; McCluskey, C.; et al. Randomized Phase II and Biomarker Study of Pembrolizumab plus Bevacizumab versus Pembrolizumab Alone for Patients with Recurrent Glioblastoma. Clin. Cancer Res. 2021, 27, 1048–1057. [Google Scholar] [CrossRef] [PubMed]
  45. Taylor, M.H.; Betts, C.B.; Maloney, L.; Nadler, E.; Algazi, A.; Guarino, M.J.; Nemunaitis, J.; Jimeno, A.; Patel, P.; Munugalavadla, V.; et al. Safety and Efficacy of Pembrolizumab in Combination with Acalabrutinib in Advanced Head and Neck Squamous Cell Carcinoma: Phase 2 Proof-of-Concept Study. Clin. Cancer Res. 2021, 28, 903–914. [Google Scholar] [CrossRef]
  46. Yarchoan, M.; Cope, L.; Ruggieri, A.N.; Anders, R.A.; Noonan, A.M.; Goff, L.W.; Goyal, L.; Lacy, J.; Li, D.; Patel, A.K.; et al. Multicenter randomized phase II trial of atezolizumab with or without cobimetinib in biliary tract cancers. J. Clin. Investig. 2021, 131, e152670. [Google Scholar] [CrossRef]
  47. Zhang, T.; Harrison, M.R.; O’Donnell, P.H.; Alva, A.S.; Hahn, N.M.; Appleman, L.J.; Cetnar, J.; Burke, J.M.; Fleming, M.T.; Milowsky, M.I.; et al. A randomized phase 2 trial of pembrolizumab versus pembrolizumab and acalabrutinib in patients with platinum-resistant metastatic urothelial cancer. Cancer 2020, 126, 4485–4497. [Google Scholar] [CrossRef]
  48. Altorki, N.K.; McGraw, T.E.; Borczuk, A.C.; Saxena, A.; Port, J.L.; Stiles, B.M.; Lee, B.E.; Sanfilippo, N.J.; Scheff, R.J.; Pua, B.B.; et al. Neoadjuvant durvalumab with or without stereotactic body radiotherapy in patients with early-stage non-small-cell lung cancer: A single-centre, randomised phase 2 trial. Lancet Oncol. 2021, 22, 824–835. [Google Scholar] [CrossRef]
  49. McBride, S.; Sherman, E.; Tsai, C.J.; Baxi, S.; Aghalar, J.; Eng, J.; Zhi, W.I.; McFarland, D.; Michel, L.S.; Young, R.; et al. Randomized Phase II Trial of Nivolumab With Stereotactic Body Radiotherapy Versus Nivolumab Alone in Metastatic Head and Neck Squamous Cell Carcinoma. J. Clin. Oncol. 2021, 39, 30–37. [Google Scholar] [CrossRef]
  50. Papadopoulos, K.P.; Johnson, M.L.; Lockhart, A.C.; Moore, K.N.; Falchook, G.S.; Formenti, S.C.; Naing, A.; Carvajal, R.D.; Rosen, L.S.; Weiss, G.J.; et al. First-In-Human Study of Cemiplimab Alone or In Combination with Radiotherapy and/or Low-dose Cyclophosphamide in Patients with Advanced Malignancies. Clin. Cancer Res. 2020, 26, 1025–1033. [Google Scholar] [CrossRef]
  51. Theelen, W.S.M.E.; Peulen, H.M.U.; Lalezari, F.; Van Der Noort, V.; De Vries, J.F.; Aerts, J.G.J.V.; Dumoulin, D.W.; Bahce, I.; Niemeijer, A.-L.N.; De Langen, A.J.; et al. Effect of Pembrolizumab After Stereotactic Body Radiotherapy vs Pembrolizumab Alone on Tumor Response in Patients With Advanced Non–Small Cell Lung Cancer: Results of the PEMBRO-RT Phase 2 Randomized Clinical Trial. JAMA Oncol. 2019, 5, 1276–1282. [Google Scholar] [CrossRef] [PubMed]
  52. Burtness, B.; Harrington, K.J.; Greil, R.; Soulières, D.; Tahara, M.; de Castro, G., Jr.; Psyrri, A.; Basté, N.; Neupane, P.; Bratland, A.; et al. Pembrolizumab alone or with chemotherapy versus cetuximab with chemotherapy for recurrent or metastatic squamous cell carcinoma of the head and neck (KEYNOTE-048): A randomised, open-label, phase 3 study. Lancet 2019, 394, 1915–1928. [Google Scholar] [CrossRef] [PubMed]
  53. Fang, W.; Yang, Y.; Ma, Y.; Hong, S.; Lin, L.; He, X.; Xiong, J.; Li, P.; Zhao, H.; Huang, Y.; et al. Camrelizumab (SHR-1210) alone or in combination with gemcitabine plus cisplatin for nasopharyngeal carcinoma: Results from two single-arm, phase 1 trials. Lancet Oncol. 2018, 19, 1338–1350. [Google Scholar] [CrossRef] [PubMed]
  54. Galsky, M.D.; Arija, J.Á.A.; Bamias, A.; Davis, I.D.; De Santis, M.; Kikuchi, E.; Garcia-Del-Muro, X.; De Giorgi, U.; Mencinger, M.; Izumi, K.; et al. Atezolizumab with or without chemotherapy in metastatic urothelial cancer (IMvigor130): A multicentre, randomised, placebo-controlled phase 3 trial. Lancet 2020, 395, 1547–1557. [Google Scholar] [CrossRef]
  55. Levy, B.P.; Giaccone, G.; Besse, B.; Felip, E.; Garassino, M.C.; Gomez, M.D.; Garrido, P.; Piperdi, B.; Ponce-Aix, S.; Menezes, D.; et al. Randomised phase 2 study of pembrolizumab plus CC-486 versus pembrolizumab plus placebo in patients with previously treated advanced non-small cell lung cancer. Eur. J. Cancer 2019, 108, 120–128. [Google Scholar] [CrossRef]
  56. Nie, J.; Wang, C.; Liu, Y.; Yang, Q.; Mei, Q.; Dong, L.; Li, X.; Liu, J.; Ku, W.; Zhang, Y.; et al. Addition of Low-Dose Decitabine to Anti–PD-1 Antibody Camrelizumab in Relapsed/Refractory Classical Hodgkin Lymphoma. J. Clin. Oncol. 2019, 37, 1479–1489. [Google Scholar] [CrossRef]
  57. Powles, T.; Csőszi, T.; Özgüroğlu, M.; Matsubara, N.; Géczi, L.; Cheng, S.Y.-S.; Fradet, Y.; Oudard, S.; Vulsteke, C.; Barrera, R.M.; et al. Pembrolizumab alone or combined with chemotherapy versus chemotherapy as first-line therapy for advanced urothelial carcinoma (KEYNOTE-361): A randomised, open-label, phase 3 trial. Lancet Oncol. 2021, 22, 931–945. [Google Scholar] [CrossRef]
  58. Shitara, K.; Van Cutsem, E.; Bang, Y.-J.; Fuchs, C.; Wyrwicz, L.; Lee, K.-W.; Kudaba, I.; Garrido, M.; Chung, H.C.; Lee, J.; et al. Efficacy and Safety of Pembrolizumab or Pembrolizumab Plus Chemotherapy vs Chemotherapy Alone for Patients With First-line, Advanced Gastric Cancer: The KEYNOTE-062 Phase 3 Randomized Clinical Trial. JAMA Oncol. 2020, 6, 1571–1580. [Google Scholar] [CrossRef] [PubMed]
  59. Ueno, M.; Ikeda, M.; Morizane, C.; Kobayashi, S.; Ohno, I.; Kondo, S.; Okano, N.; Kimura, K.; Asada, S.; Namba, Y.; et al. Nivolumab alone or in combination with cisplatin plus gemcitabine in Japanese patients with unresectable or recurrent biliary tract cancer: A non-randomised, multicentre, open-label, phase 1 study. Lancet Gastroenterol. Hepatol. 2019, 4, 611–621. [Google Scholar] [CrossRef]
  60. Gutierrez, M.; Moreno, V.; Heinhuis, K.M.; Olszanski, A.J.; Spreafico, A.; Ong, M.; Chu, Q.S.; Carvajal, R.D.; Trigo, J.; Ochoa de Olza, M.; et al. OX40 Agonist BMS-986178 Alone or in Combination With Nivolumab and/or Ipilimumab in Patients With Advanced Solid Tumors. Clin. Cancer Res. 2021, 27, 460–472. [Google Scholar] [CrossRef]
  61. Spigel, D.; Jotte, R.; Nemunaitis, J.; Shum, M.; Schneider, J.; Goldschmidt, J.; Eisenstein, J.; Berz, D.; Seneviratne, L.; Socoteanu, M.; et al. Randomized Phase 2 Studies of Checkpoint Inhibitors Alone or in Combination With Pegilodecakin in Patients With Metastatic NSCLC (CYPRESS 1 and CYPRESS 2). J. Thorac. Oncol. 2021, 16, 327–333. [Google Scholar] [CrossRef] [PubMed]
  62. Garuti, F.; Neri, A.; Avanzato, F.; Gramenzi, A.; Rampoldi, D.; Rucci, P.; Farinati, F.; Giannini, E.G.; Piscaglia, F.; Rapaccini, G.L.; et al. The changing scenario of hepatocellular carcinoma in Italy: An update. Liver Int. 2021, 41, 585–597. [Google Scholar] [CrossRef] [PubMed]
  63. Research C for DE and. Clinical Trial Endpoints for the Approval of Cancer Drugs and Biologics. U.S. Food and Drug Ad-ministration. Published 25 January 2021. Available online: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/clinical-trial-endpoints-approval-cancer-drugs-and-biologics (accessed on 7 May 2022).
  64. Xu, Y.; Hezam, K.; Ali, M.G.; Wang, Y.; Zhang, J. The efficacy and safety of Nivolumab combined with Ipilimumab in the immunotherapy of cancer: A meta-analysis. Immunopharmacol. Immunotoxicol. 2021, 43, 386–394. [Google Scholar] [CrossRef] [PubMed]
  65. Chemotherapy Plus Immune Check-Point Inhibitors in Metastatic Bladder Cancer—IOS Press. Available online: https://content.iospress.com/articles/bladder-cancer/blc190260 (accessed on 7 May 2022).
  66. Yang, Y.; Jin, G.; Pang, Y.; Huang, Y.; Wang, W.; Zhang, H.; Tuo, G.; Wu, P.; Wang, Z.; Zhu, Z. Comparative Efficacy and Safety of Nivolumab and Nivolumab Plus Ipilimumab in Advanced Cancer: A Systematic Review and Meta-Analysis. Front. Pharmacol. 2020, 11, 40. [Google Scholar] [CrossRef]
  67. Espíndola, L.M.; Salhab, R.M.; Dos Anjos, C.; Garicochea, B.; Munhoz, R.R. Is It Better to Use Ipilimumab Combined With a PD-1 Inhibitor or a PD-1 Inhibitor Alone as Initial Immunotherapy in Patients With Metastatic Melanoma? Clin. Ski. Cancer 2017, 2, 10–17. [Google Scholar] [CrossRef]
  68. Hellmann, M.D.; Paz-Ares, L.; Bernabe Caro, R.; Zurawski, B.; Kim, S.-W.; Carcereny Costa, E.; Park, K.; Alexandru, A.; Lupinacci, L.; de la Mora Jimenez, E.; et al. Nivolumab plus Ipilimumab in Advanced Non–Small-Cell Lung Cancer. N. Engl. J. Med. 2019, 381, 2020–2031. [Google Scholar] [CrossRef]
  69. Baruch, E.N.; Youngster, I.; Ben-Betzalel, G.; Ortenberg, R.; Lahat, A.; Katz, L.; Adler, K.; Dick-Necula, D.; Raskin, S.; Bloch, N.; et al. Fecal microbiota transplant promotes response in immunotherapy-refractory melanoma patients. Science 2020, 371, 602–609. [Google Scholar] [CrossRef]
  70. Janney, A.; Powrie, F.; Mann, E.H. Host–microbiota maladaptation in colorectal cancer. Nature 2020, 585, 509–517. [Google Scholar] [CrossRef]
  71. Zhou, S.; Khanal, S.; Zhang, H. Risk of immune-related adverse events associated with ipilimumab-plus-nivolumab and nivolumab therapy in cancer patients. Ther. Clin. Risk Manag. 2019, 15, 211–221. [Google Scholar] [CrossRef] [Green Version]
  72. Ji, H.-H.; Tang, X.-W.; Dong, Z.; Song, L.; Jia, Y.-T. Adverse Event Profiles of Anti-CTLA-4 and Anti-PD-1 Monoclonal Antibodies Alone or in Combination: Analysis of Spontaneous Reports Submitted to FAERS. Clin. Drug Investig. 2019, 39, 319–330. [Google Scholar] [CrossRef]
  73. Abdelhafeez, A.; Shohdy, K.S.; Ibrahim, W. Safety of Combination Immune Checkpoint Inhibitors Compared to Monotherapy; A Systematic Review and Meta-Analysis. Cancer Investig. 2020, 38, 150–157. [Google Scholar] [CrossRef] [PubMed]
  74. Cramer, J.D.; Burtness, B.; Ferris, R.L. Immunotherapy for head and neck cancer: Recent advances and future directions. Oral Oncol. 2019, 99, 104460. [Google Scholar] [CrossRef]
  75. Taylor, M.H.; Lee, C.-H.; Makker, V.; Rasco, D.; Dutcus, C.E.; Wu, J.; Stepan, D.E.; Shumaker, R.C.; Motzer, R.J. Phase IB/II Trial of Lenvatinib Plus Pembrolizumab in Patients With Advanced Renal Cell Carcinoma, Endometrial Cancer, and Other Selected Advanced Solid Tumors. J. Clin. Oncol. 2020, 38, 1154–1163. [Google Scholar] [CrossRef]
  76. Hussaini, S.; Chehade, R.; Boldt, R.G.; Raphael, J.; Blanchette, P.; Vareki, S.M.; Fernandes, R. Association between immune-related side effects and efficacy and benefit of immune checkpoint inhibitors—A systematic review and meta-analysis. Cancer Treat. Rev. 2021, 92, 102134. [Google Scholar] [CrossRef] [PubMed]
  77. Oh, A.; Tran, D.M.; McDowell, L.C.; Keyvani, D.; Barcelon, J.A.; Merino, O.; Wilson, L. Cost-Effectiveness of Nivolumab-Ipilimumab Combination Therapy Compared with Monotherapy for First-Line Treatment of Metastatic Melanoma in the United States. J. Manag. Care Spéc. Pharm. 2017, 23, 653–664. [Google Scholar] [CrossRef] [Green Version]
  78. Facciorusso, A.; Del Prete, V.; Crucinio, N.; Serviddio, G.; Vendemiale, G.; Muscatiello, N. Lymphocyte-to-monocyte ratio predicts survival after radiofrequency ablation for colorectal liver metastases. World J. Gastroenterol. 2016, 22, 4211–4218. [Google Scholar] [CrossRef] [PubMed]
  79. Nishijima, T.F.; Muss, H.B.; Shachar, S.S.; Tamura, K.; Takamatsu, Y. Prognostic value of lymphocyte-to-monocyte ratio in patients with solid tumors: A systematic review and meta-analysis. Cancer Treat. Rev. 2015, 41, 971–978. [Google Scholar] [CrossRef] [PubMed]
  80. Chang, Z.; Zheng, J.; Ma, Y.; Zhao, J.; Wang, C.; Liu, Z. The neutrophil-to-lymphocyte ratio as a predictor for recurrence of colorectal liver metastases following radiofrequency ablation. Med. Oncol. 2014, 31, 855. [Google Scholar] [CrossRef]
  81. Jia, W.; Wu, J.; Jia, H.; Yang, Y.; Zhang, X.; Chen, K.; Su, F. The Peripheral Blood Neutrophil-To-Lymphocyte Ratio Is Superior to the Lymphocyte-To-Monocyte Ratio for Predicting the Long-Term Survival of Triple-Negative Breast Cancer Patients. PLoS ONE 2015, 10, e0143061. [Google Scholar] [CrossRef]
  82. Ayers, M.; Lunceford, J.; Nebozhyn, M.; Murphy, E.; Loboda, A.; Kaufman, D.R.; Albright, A.; Cheng, J.D.; Kang, S.P.; Shankaran, V.; et al. IFN-γ–related mRNA profile predicts clinical response to PD-1 blockade. J. Clin. Investig. 2017, 127, 2930–2940. [Google Scholar] [CrossRef]
  83. Hashimoto, K.; Nishimura, S.; Ito, T.; Akagi, M. Characterization of PD-1/PD-L1 immune checkpoint expression in soft tissue sarcomas. Eur. J. Histochem. 2021, 65, 3203. [Google Scholar] [CrossRef] [PubMed]
  84. Upadhaya, S.; Neftelino, S.T.; Hodge, J.P.; Oliva, C.; Campbell, J.R.; Yu, J.X. Combinations take centre stage in PD1/PDL1 inhibitor clinical trials. Nat. Rev. Drug Discov. 2021, 20, 168–169. [Google Scholar] [CrossRef] [PubMed]
  85. Garon, E.B.; Rizvi, N.A.; Hui, R.; Leighl, N.; Balmanoukian, A.S.; Eder, J.P.; Patnaik, A.; Aggarwal, C.; Gubens, M.; Horn, L.; et al. Pembrolizumab for the Treatment of Non–Small-Cell Lung Cancer. N. Engl. J. Med. 2015, 372, 2018–2028. [Google Scholar] [CrossRef] [PubMed]
  86. Doroshow, D.B.; Bhalla, S.; Beasley, M.B.; Sholl, L.M.; Kerr, K.M.; Gnjatic, S.; Wistuba, I.I.; Rimm, D.L.; Tsao, M.S.; Hirsch, F.R. PD-L1 as a biomarker of response to immune-checkpoint inhibitors. Nat. Rev. Clin. Oncol. 2021, 18, 345–362. [Google Scholar] [CrossRef]
Cancers 15 00682 g001 550
Figure 1. Flow chart of study selection.
Figure 1. Flow chart of study selection.
Cancers 15 00682 g001
Cancers 15 00682 g002 550
Figure 2. Forest Plot of the Risk ratio of ORR based on therapeutic schedules: anti-PD-1/PD-L1 versus combination therapy (immunotherapy, targeted therapy, radiotherapy, chemotherapy, and other drugs). Boyer 2021 [12], Ferris 2020 [17], Gettinger 2021 [18], Janjigian 2018 [19], Kelley 2021 [21], Kelly 2019 [22], Long 2018 [23], Long 2019 [24], Omuro 2017 [25], O’Reilly 2019 [26], Paz-Ares 2021 [27], Planchard 2020 [28], Powles 2020 [29], Ready 2019 [30], Scherpereel 2019 [31], Sharma 2019 [33], Singh 2021 [34], Siu 2018 [35], Wolchok 2021 [37], Zamarin 2020 [38], Eng 2019 [40], Gogas 2020 [41], Lee 2020 [42], McDermott 2018 [43], Nayak 2020 [44], Taylor 2022 [45], Yarchoan 2021 [46], Zhang 2020 [47], Altorki 2021 [48], McBride 2020 [49], Papadopoulos 2019 [50], Theelen 2019 [51], Burtness 2019 [52], Fang 2018 [53], Galsky 2020 [54], Levy 2019 [55], Nie 2019 [56], Powles 2021 [57], Shitara 2020 [58], Ueno 2019 [59], Gutierrez 2020 [60], Spigel 2020 [61].
Figure 2. Forest Plot of the Risk ratio of ORR based on therapeutic schedules: anti-PD-1/PD-L1 versus combination therapy (immunotherapy, targeted therapy, radiotherapy, chemotherapy, and other drugs). Boyer 2021 [12], Ferris 2020 [17], Gettinger 2021 [18], Janjigian 2018 [19], Kelley 2021 [21], Kelly 2019 [22], Long 2018 [23], Long 2019 [24], Omuro 2017 [25], O’Reilly 2019 [26], Paz-Ares 2021 [27], Planchard 2020 [28], Powles 2020 [29], Ready 2019 [30], Scherpereel 2019 [31], Sharma 2019 [33], Singh 2021 [34], Siu 2018 [35], Wolchok 2021 [37], Zamarin 2020 [38], Eng 2019 [40], Gogas 2020 [41], Lee 2020 [42], McDermott 2018 [43], Nayak 2020 [44], Taylor 2022 [45], Yarchoan 2021 [46], Zhang 2020 [47], Altorki 2021 [48], McBride 2020 [49], Papadopoulos 2019 [50], Theelen 2019 [51], Burtness 2019 [52], Fang 2018 [53], Galsky 2020 [54], Levy 2019 [55], Nie 2019 [56], Powles 2021 [57], Shitara 2020 [58], Ueno 2019 [59], Gutierrez 2020 [60], Spigel 2020 [61].
Cancers 15 00682 g002
Cancers 15 00682 g003 550
Figure 3. Forest Plot of the Risk ratio of DCR based on therapeutic schedules: anti-PD-1/PD-L1 versus combination therapy (immunotherapy, targeted therapy, radiotherapy, chemotherapy, and other drugs). Boyer 2021 [12], Ferris 2020 [17], Janjigian 2018 [19], Kelley 2021 [21], Kelly 2019 [22], Long 2018 [23], Long 2019 [24], Omuro 2017 [25], O’Reilly 2019 [26], Paz-Ares 2021 [27], Powles 2020 [29], Ready 2019 [30], Scherpereel 2019 [31], Sharma 2019 [33], Singh 2021 [34], Siu 2018 [35], Wolchok 2021 [37], Zamarin 2020 [38], Eng 2019 [40], Gogas 2020 [41], Lee 2020 [42], Taylor 2022 [45], Yarchoan 2021 [46], Zhang 2020 [47], Altorki 2021 [48], Papadopoulos 2019 [50], Theelen 2019 [51], Burtness 2019 [52], Fang 2018 [53], Galsky 2020 [54], Levy 2019 [55], Powles 2021 [57], Ueno 2019 [59], Gutierrez 2020 [60], Spigel 2020 [61].
Figure 3. Forest Plot of the Risk ratio of DCR based on therapeutic schedules: anti-PD-1/PD-L1 versus combination therapy (immunotherapy, targeted therapy, radiotherapy, chemotherapy, and other drugs). Boyer 2021 [12], Ferris 2020 [17], Janjigian 2018 [19], Kelley 2021 [21], Kelly 2019 [22], Long 2018 [23], Long 2019 [24], Omuro 2017 [25], O’Reilly 2019 [26], Paz-Ares 2021 [27], Powles 2020 [29], Ready 2019 [30], Scherpereel 2019 [31], Sharma 2019 [33], Singh 2021 [34], Siu 2018 [35], Wolchok 2021 [37], Zamarin 2020 [38], Eng 2019 [40], Gogas 2020 [41], Lee 2020 [42], Taylor 2022 [45], Yarchoan 2021 [46], Zhang 2020 [47], Altorki 2021 [48], Papadopoulos 2019 [50], Theelen 2019 [51], Burtness 2019 [52], Fang 2018 [53], Galsky 2020 [54], Levy 2019 [55], Powles 2021 [57], Ueno 2019 [59], Gutierrez 2020 [60], Spigel 2020 [61].
Cancers 15 00682 g003
Cancers 15 00682 g004 550
Figure 4. Forest Plot of the Hazard ratio of OS based on therapeutic schedules: anti-PD-1/PD-L1 versus combination therapy (immunotherapy, targeted therapy, radiotherapy, chemotherapy, and other drugs). Boyer 2021 [12], Gettinger 2021 [18], Long 2019 [24], Planchard 2020 [28], Siu 2018 [35], Wolchok 2021 [37], Zamarin 2020 [38], Gogas 2020 [41], Theelen 2019 [51], Levy 2019 [55], Spigel 2020 [61].
Figure 4. Forest Plot of the Hazard ratio of OS based on therapeutic schedules: anti-PD-1/PD-L1 versus combination therapy (immunotherapy, targeted therapy, radiotherapy, chemotherapy, and other drugs). Boyer 2021 [12], Gettinger 2021 [18], Long 2019 [24], Planchard 2020 [28], Siu 2018 [35], Wolchok 2021 [37], Zamarin 2020 [38], Gogas 2020 [41], Theelen 2019 [51], Levy 2019 [55], Spigel 2020 [61].
Cancers 15 00682 g004
Table
Table 1. Main characteristic of included studies.
Table 1. Main characteristic of included studies.
AuthorPhaseTumorSample SizeInterventionsPMIDRN
ExperimentalControl
Boyer 2021 [12]IIINSCLC284284Pembrolizumab + IpilimumabPembrolizumab + Placebo33513313NCT03302234
D’Angelo 2018 [15]IISarcoma4243Nivolumab + IpilimumabNivolumab29370992NCT02500797
Ferrarotto 2020 [16]IOropharynx cancer1415Durvalumab + TremelimumabDurvalumab32269052NCT03144778
Ferris 2020 [17]IIIHNSCC247240Durvalumab + TremelimumabDurvalumab32294530NCT02369874
Gettinger 2021 [18]IIINSCLC125127Nivolumab + ipilimumabNivolumab34264316NCT02785952
Janjigian 2018 [19]I/IIEsophagogastric cancer5259Nivolumab + ipilimumabNivolumab30110194NCT01928394
Kaseb 2022 [20]IIHCC1413 Nivolumab + ipilimumabNivolumab35065057NCT03222076
Kelley 2021 [21]I/IIHCC75104Durvalumab + tremelimumabDurvalumab34292792NCT02519348
Kelly 2019 [22]Ib/IIGastric or GEJ cancer2724Durvalumab + tremelimumabDurvalumab31676670NCT02340975
Long 2018 [23]IIMelanoma3525Nivolumab + ipilimumabNivolumab29602646NCT02374242
Long 2019 [24]IIIMelanoma354352Pembrolizumab + EpacadostatPembrolizumab + Placebo31221619NCT02752074
Omuro 2017 [25]IMlioblastoma1010 Nivolumab + IpilimumabNivolumab29106665NCT02017717
O’Reilly 2019 [26]IImPDAC3232Durvalumab + TremelimumabDurvalumab31318392NCT02558894
Paz-Ares 2021 [27]IIINSCLC396396Nivolumab + IpilimumabNivolumab34648948NCT02477826
Planchard 2020 [28]IIINSCLC174117Durvalumab + TremelimumabDurvalumab32201234NCT02352948
Powles 2020 [29]IIIUrothelial carcinoma342346Durvalumab + TremelimumabDurvalumab32971005NCT02516241
Ready 2019 [30]I/IISCLC96147Nivolumab + IpilimumabNivolumab31629915NCT01928394
Scherpereel 2019 [31]IIMPM6263 Nivolumab + IpilimumabNivolumab30660609NCT02716272
Schoenfeld 2020 [32]IIOCSCC1514Nivolumab + IpilimumabNivolumab32852531NCT02919683
Sharma 2019 [33]I/IIUrothelial carcinoma10478Nivolumab + IpilimumabNivolumab31100038NCT01928394
Singh 2021 [34]IIGIST1619 Nivolumab + IpilimumabNivolumab34407970NCT02880020
Siu 2018 [35]IIHNSCC13367Durvalumab + TremelimumabDurvalumab30383184NCT02319044
Tawbi 2022 [36]II/IIIMelanoma355359Nivolumab + RelatlimabNivolumab34986285NCT03470922
Wolchok 2021 [37]IIIMelanoma314316Nivolumab + IpilimumabNivolumab34818112NCT01844505
Zamarin 2020 [38]IIEOC5149Nivolumab + IpilimumabNivolumab32275468NCT02498600
Zimmer 2020 [39]IIMelanoma5659Nivolumab + IpilimumabNivolumab32416781NCT02523313
Eng 2019 [40]IIIColorectal cancer18390Atezolizumab + CobimetinibAtezolizumab31003911NCT02788279
Gogas 2020 [41]IIIMelanoma222224Atezolizumab + CobimetinibPembrolizumab33309774NCT03273153
Lee 2020 [42]IbHCC6059Atezolizumab + BevacizumabAtezolizumab32502443NCT02715531
McDermott 2018 [43]IIRCC101103Atezolizumab + BevacizumabAtezolizumab29867230NCT01984242
Nayak 2020 [44]IIGlioblastoma5030Pembrolizumab + BevacizumabPembrolizumab33199490NCT02337491
Taylor 2022 [45]IIHNSCC3739Pembrolizumab + AcalabrutinibPembrolizumab34862248NCT02454179
Yarchoan 2021 [46]IIBTC3839Atezolizumab + CobimetinibAtezolizumab34907910NCT03201458
Zhang 2020 [47]IIUrothelial carcinoma4035Pembrolizumab + AcalabrutinibPembrolizumab32757302NCT02351739
Altorki 2021 [48]IINSCLC3030Durvalumab + SBRTDurvalumab34015311NCT02904954
McBride 2020 [49]IIHNSCC3230Nivolumab + SBRTNivolumab32822275NCT02684253
Papadopoulos 2019 [50]ISolid Tumors2418Cemiplimab + hfRTCemiplimab31796520NCT02383212
Theelen 2019 [51]IINSCLC3640Pembrolizumab + SBRTPembrolizumab 31294749NCT02492568
Burtness 2019 [52]IIIHNSCC281301Pembrolizumab + ChemotherapyPembrolizumab31679945NCT02358031
Fang 2018 [53]INPC2393Camrelizumab + ChemotherapyCamrelizumab30213452NCT02721589NCT03121716
Galsky 2020 [54]IIIUrothelial carcinoma451362Atezolizumab + ChemotherapyAtezolizumab32416780NCT02807636
Levy 2019 [55]IINSCLC5149Pembrolizumab + CC-486Pembrolizumab + Placebo30654297NCT02546986
Nie 2019 [56]IIcHL4219Camrelizumab + DecitabineCamrelizumab31039052NCT02961101NCT03250962
Powles 2021 [57]IIIUrothelial carcinoma351307Pembrolizumab + ChemotherapyPembrolizumab34051178NCT02853305
Shitara 2020 [58]IIIGastric Cancer257256Pembrolizumab + ChemotherapyPembrolizumab32880601NCT02494583
Ueno 2019 [59]IBTC3030Nivolumab + ChemotherapyNivolumab31109808JapicCTI-153098
Gutierrez 2020 [60]I/IIaBladder cancer62BMS-986178 + NivolumabNivolumab33148673NCT02737475
Spigel 2020 [61]IINSCLC5150Pembrolizumab + PegilodecakinPembrolizumab33166722NCT03382899NCT03382912
Abbreviations: NSCLC, non-small cell lung cancer; HNSCC, head and neck squamous cell carcinoma; HCC, hepatocellular carcinoma; GEJ, gastroesophageal junction; mPDAC, metastatic pancreatic ductal adenocarcinoma; SCLC, small cell lung cancer; MPM, malignant pleural mesothelioma; OCSCC, Oral Cavity Squamous Cell Carcinoma; GIST, Gastrointestinal Stromal Tumors; EOC, epithelial ovarian cancer; RCC, renal cell carcinoma; BTC, biliary tract cancer; NPC, nasopharyngeal carcinoma; cHL, classic Hodgkin lymphoma; SBRT, stereotactic body radiotherapy; hfRT, hypofractionated radiotherapy, PMID, PubMed Unique Identifier; RN, Registration Number. Three studies had the same NCT number because the clinical trial investigated six tumor types simultaneously and published multiple articles with the same number (NCT01928394). One study analyzed two single-arm phase 1 trials of patients with nasopharyngeal carcinoma and had the same primary outcome indicators, but was a non-randomized controlled trial (NCT02721589, NCT03121716). Both clinical trials enrolled in this single-center study investigated anti-PD-L1 alone or in combination with decitabine for Hodgkin’s lymphoma, with essentially identical inclusion and exclusion criteria and the same primary endpoint (NCT02961101, NCT03250962). The study included two NCT numbers (NCT03382899, NCT03382912) because Pegilodecakin combined two kinds of PD-L1. Since both cohorts had the same outcome, we selected the larger cohort for statistical purposes (NCT03382899).
Table
Table 2. Median survival ratio of OS based on therapeutic schedules.
Table 2. Median survival ratio of OS based on therapeutic schedules.
Subgroup and Author (Year)ES[95% Conf. Interval]%Weight
PD-1 + Immunotherapy vs. PD-1
Omuro 2017 [25]0.8850.5641.3872.17
Schrpereel 2019 [31]1.3361.1211.5923.35
Singh 2021 [34]0.3270.2350.4562.68
Zamarin 2020 [38]1.2891.0601.5683.27
Planchard 2020 [28]1.1501.0251.2903.55
O’Reilly 2019 [26]0.8610.6751.0983.08
Wolchok 2021 [37]1.9541.8072.1133.64
Siu 2018 [35]1.2671.1001.4583.48
Paz-Ares 2021 [27]1.0891.0161.1683.66
Boyer 2021 [12]0.9770.9001.0613.63
Ready 2019 [30]0.8250.7270.9353.52
Sharma 2019 [33]0.7470.6460.8643.46
Ferris 2020 [17]0.8550.7830.9353.62
Kelley 2021 [21]1.2381.0701.4343.46
Kelly 2019 [22]2.7062.0563.5602.94
D’Angelo 2018 [15]1.3361.0811.6533.21
Gettinger 2021 [18]0.9090.8041.0293.53
Powles 2020 [29]1.1441.0621.2333.65
Janjigian 2018 [19]0.7740.6430.9323.31
Subgroup, DL1.0590.9201.22063.20
PD-1 + target therapy vs. PD-1
Eng 2019 [40]1.2491.1101.4073.54
Nayak 2020 [44]0.8540.6861.0643.18
Taylor 2022 [45]1.0100.8071.2653.16
Zhang 2020 [47]0.5530.4410.6933.15
Subgroup, DL0.8850.6201.26213.03
PD-1 + radiotherapy vs. PD-1
McBride 2020 [49]0.9790.7601.2613.03
Theelen 2019 [51]2.0921.6712.6203.16
Subgroup, DL1.4340.6813.0196.19
PD-1 + chemotherapy vs. PD-1
Burtness 2019 [52]0.8720.8040.9463.63
Shitara 2020 [58]1.1791.0811.2863.62
Ueno 2019 [59]2.9622.2993.8143.03
Galsky 2020 [54]1.0190.9511.0923.66
Powles 2021 [57]1.0901.0101.1763.64
Subgroup, DL1.2221.0061.48417.59
Overall, DL1.0860.9801.203100.00
Tests of subgroup effect size = 1; Cochran’s Q statistics for heterogeneity; PD-1 + immunotherapy vs. PD-1: z =0.797, p= 0.426; I2 =95.8%; PD-1 + target therapy vs. PD-1: z =-0.676, p = 0.499; I2= 92.8%; PD-1 + radiotherapy vs. PD-1: z =0.950, p = 0.342; I2 = 94.8%; PD-1 + chemotherapy vs. PD-1: z =2.024, p = 0.043; I2 = 95.7%; Overall: z =1.568, p = 0.117; I2 = 95.2%; Between: p = 0.343.
Table
Table 3. Median survival ratio of PFS based on therapeutic schedules.
Table 3. Median survival ratio of PFS based on therapeutic schedules.
Subgroup and Author (Year)ES[95% Conf. Interval]% Weight
PD-1 + Immunotherapy vs. PD-1
Kaseb 2022 [20]2.0781.4253.0302.29
Omuro 2017 [25]0.7890.5041.2382.13
Scherpereel 2019 [31]1.4001.1751.6682.67
Singh 2021 [34]0.7100.5100.9892.39
Zamarin 2020 [38]1.9501.6032.3722.64
Planchard 2020 [28]1.1291.0061.2662.74
O’Reilly 2019 [26]1.0000.7841.2752.56
Long 2019 [24]0.9590.8911.0332.77
Long 2018 [23]5.3084.1216.8362.54
Tawbi 2022 [36]2.1962.0402.3632.77
Wolchok 2021 [37]1.6671.5411.8022.77
Siu 2018 [35]1.0530.9141.2122.71
Paz-Ares 2021 [27]1.2141.1331.3022.77
Boyer 2021 [12]0.9760.8991.0602.76
Ready 2019 [30]1.0710.9451.2152.73
Sharma 2019 [33]0.9290.8031.0742.70
Kelley 2021 [21]1.0480.9051.2142.70
Kelly 2019 [22]1.1250.8551.4802.50
D’Angelo 2018 [15]2.4121.9502.9832.61
Gettinger 2021 [18]1.3101.1581.4832.73
Powles 2020 [29]1.6091.493 1.7342.77
Janjigian 2018 [19]1.1430.9491.3772.65
Subgroup, DL1.3371.1571.54457.88
PD-1 + target therapy vs. PD-1
Eng 2019 [40]0.9850.8741.1092.73
McDermott 2018 [43]1.9181.6722.2002.71
Gogas 2020 [41]0.9650.8761.0632.75
Nayak 2020 [44]2.8672.3033.5702.60
Yarchoan 2021 [46]1.9521.5332.4842.56
Taylor 2022 [45]1.5881.2681.9892.59
Lee 2020 [42]1.6471.3761.9712.66
Zhang 2020 [47]1.3751.0971.7242.59
Subgroup, DL1.5591.1892.04421.20
PD-1 + radiotherapy vs. PD-1
Papadopoulos 2019 [50]1.5831.1702.1422.45
McBride 2020 [49]1.3681.0631.7622.54
Theelen 2019 [51]3.4742.7744.3492.59
Subgroup, DL1.9681.068 3.6257.58
PD-1 + chemotherapy vs. PD-1
Burtness 2019 [52]2.1301.9642.3112.76
Levy 2019 [55]0.7250.5960.8822.64
Shitara 2020 [58]3.4503.1643.7622.76
Ueno 2019 [59]3.0002.3293.8642.54
Subgroup, DL2.0041.1783.40810.70
PD-1 + other vs. PD-1
Spigel 2020 [61]1.0330.8501.2552.64
Subgroup, DL1.0330.8501.2552.64
Overall, DL1.4751.2901.688100.00
Tests of subgroup effect size = 1; Cochran’s Q statistics for heterogeneity. PD-1 + immunotherapy vs. PD-1: z =3.950, p = 0.000; I2 = 96.7%; PD-1 + target therapy vs. PD-1: z =3.211, p = 0.001; I2 =95.6%; PD-1 + radiotherapy vs. PD-1: z =2.171, p = 0.030; I2 =94.0%; PD-1 + chemotherapy vs. PD-1: z =2.564, p = 0.010; I2 = 98.6%; PD-1 + other vs. PD-1: z =0.324, p = 0.746; Overall: z =5.674, p = 0.000; I2 =97.5%; Between: p = 0.021.
Table
Table 4. Subgroup analysis of any grade adverse events.
Table 4. Subgroup analysis of any grade adverse events.
Experimental vs. ControlNo. of StudiesRR95% CIpHeterogeneity (I2)
Any grade adverse events381.13[1.08, 1.18]<0.00189%
Any grade fatigue421.31[1.15, 1.50]<0.00162%
Any grade diarrhea371.87[1.58, 2.21]<0.00159%
Any grade rash371.81[1.51, 2.16]<0.00164%
Any grade pruritus 341.48[1.34, 1.64]<0.00139%
Any grade nausea311.75[1.32, 2.33]<0.00180%
Any grade thyroid abnormalities311.22[1.11, 1.35]<0.00126%
Any grade decreased appetite301.59[1.27, 2.00]<0.00169%
Any grade elevated enzymes291.93[1.61, 2.33]<0.00158%
Any grade hypothyroidism271.2[1.06, 1.35]0.0037%
Any grade pain271.24[1.03, 1.49]0.0256%
Any grade anemia262.03[1.54, 2.67]<0.00168%
Any grade pyrexia 251.89[1.44, 2.48]<0.00155%
Any grade vomiting222.34[1.77, 3.08]<0.00156%
Any grade decreased white-cell count202.56[1.16, 5.67]0.0283%
Any grade decreased platelet count192.83[1.27, 6.29]0.0180%
Any grade constipation181.79[1.35, 2.38]<0.00163%
Any grade asthenia151.51[1.32, 1.72]<0.00123%
Any grade infection 111.65[1.36, 2.01]<0.00112%
Any grade serious event 111.44[1.21, 1.72]<0.00157%
Any grade treatment-related Adverse Events Leading to Discontinuation 111.83[1.46, 2.29]<0.0010
Any grade treatment-related serious adverse events102.35[1.97, 2.81]<0.00111%
Table
Table 5. Subgroup analysis of 3–5 grade adverse events.
Table 5. Subgroup analysis of 3–5 grade adverse events.
Experimental vs. ControlNo. of StudiesRR95% CIpHeterogeneity(I2)
3–5 grade adverse events391.81[1.63, 2.01]<0.00177%
3–5 grade fatigue 411.93[1.71, 2.18]<0.00139%
3–5 grade diarrhea343.35[2.46, 4.57]<0.0016%
3–5 grade rash342.07[1.45, 2.93]<0.00131%
3–5 grade pruritus312[0.89, 4.46]=0.090%
3–5 grade elevated enzymes302.05[1.44, 2.92]<0.00155%
3–5 grade nausea 293.06[2.02, 4.65]<0.00137%
3–5 grade decreased appetite282.06[1.35, 3.16]<0.00124%
3–5 grade thyroid abnormalities271.82[0.83, 3.97]0.130%
3–5 grade anemia 254.51[2.64, 7.70]<0.00160%
3–5 grade pain250.97[0.66, 1.43]0.880%
3–5 grade hypothyroidism 241.13[0.40, 3.18]0.810%
3–5 grade decreased white-cell count213.44[1.06, 11.19]0.0454%
3–5 grade pyrexia212.67[1.42, 5.05]0.0020%
3–5 grade vomiting203.91[1.51, 10.07]0.00563%
3–5 grade decreased platelet count196.12[1.86, 20.16]0.00366%
3–5 grade asthenia172.39[1.68, 3.40]<0.0018%
3–5 grade constipation170.82[0.36, 1.90]0.650%
3–5 grade infection 121.25[1.00, 1.55]0.0535%
3–5 grade treatment-related Adverse Events Leading to Discontinuation83.4[2.26, 5.12]<0.0010%
3–5 grade treatment-related serious adverse events62.84[1.65, 4.86]<0.0010%
3–5 serious event42.29[1.48, 3.53]<0.0010%
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Zhang, Y.; Yao, Q.; Pan, Y.; Fang, X.; Xu, H.; Zhao, T.; Zhu, G.; Jiang, T.; Li, S.; Cao, H. Efficacy and Safety of PD-1/PD-L1 Checkpoint Inhibitors versus Anti-PD-1/PD-L1 Combined with Other Therapies for Tumors: A Systematic Review. Cancers 2023, 15, 682. https://doi.org/10.3390/cancers15030682

AMA Style

Zhang Y, Yao Q, Pan Y, Fang X, Xu H, Zhao T, Zhu G, Jiang T, Li S, Cao H. Efficacy and Safety of PD-1/PD-L1 Checkpoint Inhibitors versus Anti-PD-1/PD-L1 Combined with Other Therapies for Tumors: A Systematic Review. Cancers. 2023; 15(3):682. https://doi.org/10.3390/cancers15030682

Chicago/Turabian Style

Zhang, Yiru, Qigu Yao, Yong Pan, Xinru Fang, Haoying Xu, Tingxiao Zhao, Guangqi Zhu, Tianan Jiang, Shibo Li, and Hongcui Cao. 2023. "Efficacy and Safety of PD-1/PD-L1 Checkpoint Inhibitors versus Anti-PD-1/PD-L1 Combined with Other Therapies for Tumors: A Systematic Review" Cancers 15, no. 3: 682. https://doi.org/10.3390/cancers15030682

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop