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Comprehensive Evaluation of Anti-PD-1, Anti-PD-L1, Anti-CTLA-4 and Their Combined Immunotherapy in Clinical Trials: A Systematic Review and Meta-analysis
by
Chen, Wei
, Jiang, Bin
, Zhang, Zhengyu
, Wu, Jian
, Cen, Chao
, Wang, Ying
, Xiang, Ze
, Li, Jiayuan
, Zhai, Guanghua
, Meng, Yiling
, Berglund, Björn
in
Bayesian analysis
/ cancer immunotherapy
/ Cancer therapies
/ Chemotherapy
/ Clinical trials
/ CTLA-4 protein
/ cytotoxic T lymphocyte antigen-4 (CTLA-4)
/ Drugs
/ FDA approval
/ immune checkpoint inhibitor
/ Immune checkpoint inhibitors
/ Immunosuppressive agents
/ Immunotherapy
/ Kidney cancer
/ Lung cancer
/ Medical prognosis
/ Melanoma
/ Meta-analysis
/ Ovarian cancer
/ Patients
/ PD-1 protein
/ PD-L1 protein
/ Pembrolizumab
/ Pharmacology
/ programmed death-1 (PD-1)
/ programmed death-ligand-1 (PD-L1)
/ Squamous cell carcinoma
/ Standard of care
/ Survival
/ Systematic review
2022
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Comprehensive Evaluation of Anti-PD-1, Anti-PD-L1, Anti-CTLA-4 and Their Combined Immunotherapy in Clinical Trials: A Systematic Review and Meta-analysis
by
Chen, Wei
, Jiang, Bin
, Zhang, Zhengyu
, Wu, Jian
, Cen, Chao
, Wang, Ying
, Xiang, Ze
, Li, Jiayuan
, Zhai, Guanghua
, Meng, Yiling
, Berglund, Björn
in
Bayesian analysis
/ cancer immunotherapy
/ Cancer therapies
/ Chemotherapy
/ Clinical trials
/ CTLA-4 protein
/ cytotoxic T lymphocyte antigen-4 (CTLA-4)
/ Drugs
/ FDA approval
/ immune checkpoint inhibitor
/ Immune checkpoint inhibitors
/ Immunosuppressive agents
/ Immunotherapy
/ Kidney cancer
/ Lung cancer
/ Medical prognosis
/ Melanoma
/ Meta-analysis
/ Ovarian cancer
/ Patients
/ PD-1 protein
/ PD-L1 protein
/ Pembrolizumab
/ Pharmacology
/ programmed death-1 (PD-1)
/ programmed death-ligand-1 (PD-L1)
/ Squamous cell carcinoma
/ Standard of care
/ Survival
/ Systematic review
2022
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Do you wish to request the book?
Comprehensive Evaluation of Anti-PD-1, Anti-PD-L1, Anti-CTLA-4 and Their Combined Immunotherapy in Clinical Trials: A Systematic Review and Meta-analysis
by
Chen, Wei
, Jiang, Bin
, Zhang, Zhengyu
, Wu, Jian
, Cen, Chao
, Wang, Ying
, Xiang, Ze
, Li, Jiayuan
, Zhai, Guanghua
, Meng, Yiling
, Berglund, Björn
in
Bayesian analysis
/ cancer immunotherapy
/ Cancer therapies
/ Chemotherapy
/ Clinical trials
/ CTLA-4 protein
/ cytotoxic T lymphocyte antigen-4 (CTLA-4)
/ Drugs
/ FDA approval
/ immune checkpoint inhibitor
/ Immune checkpoint inhibitors
/ Immunosuppressive agents
/ Immunotherapy
/ Kidney cancer
/ Lung cancer
/ Medical prognosis
/ Melanoma
/ Meta-analysis
/ Ovarian cancer
/ Patients
/ PD-1 protein
/ PD-L1 protein
/ Pembrolizumab
/ Pharmacology
/ programmed death-1 (PD-1)
/ programmed death-ligand-1 (PD-L1)
/ Squamous cell carcinoma
/ Standard of care
/ Survival
/ Systematic review
2022
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Comprehensive Evaluation of Anti-PD-1, Anti-PD-L1, Anti-CTLA-4 and Their Combined Immunotherapy in Clinical Trials: A Systematic Review and Meta-analysis
Journal Article
Comprehensive Evaluation of Anti-PD-1, Anti-PD-L1, Anti-CTLA-4 and Their Combined Immunotherapy in Clinical Trials: A Systematic Review and Meta-analysis
2022
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Overview
Immunotherapy with immune checkpoint inhibitor (ICI) drugs is gradually becoming a hot topic in cancer treatment. To comprehensively evaluate the safety and efficacy of ICI drugs, we employed the Bayesian model and conducted a network meta-analysis in terms of progression-free survival (PFS), overall survival (OS) and severe adverse events (AEs). Our study found that treatment with ipilimumab was significantly worse than standard therapies in terms of PFS, whereas treatment with cemiplimab significantly improved PFS. The results also indicated that cemiplimab was the best choice for PFS. Treatment with nivolumab, pembrolizumab and nivolumab plus ipilimumab significantly improved OS compared to standard therapies. In terms of OS, cemiplimab was found to be the best choice, whereas avelumab was the worst. In terms of severe AEs, atezolizumab, avelumab, durvalumab, nivolumab, and pembrolizumab all significantly reduced the risk of grade 3 or higher AEs compared to standard therapy. The least likely to be associated with severe AEs were as follows: cemiplimab, avelumab, nivolumab, atezolizumab, and camrelizumab, with nivolumab plus ipilimumab to be the worst. Therefore, different ICI drug therapies may pose different risks in terms of PFS, OS and severe AEs. Our study may provide new insights and strategies for the clinical practice of ICI drugs.
Publisher
Frontiers Media SA,Frontiers Media S.A
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