Meta-Analysis of Efficacy From CTLA-4 and PD-1/PD-L1 Inhibitors in Cancer Patients

Immune checkpoint inhibitors (ICIs) have been approved to prolong overall survival (OS), compared to other treatments. However, the recent studies reported consistent and inconsistent results. Hence, we conducted this meta-analysis to evaluate the efficacy of ICIs. The articles were identified by se...

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Published inFrontiers in oncology Vol. 12; p. 876098
Main Authors Xu, Li, Yan, Xin, Ding, Weiyue
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 28.04.2022
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Abstract Immune checkpoint inhibitors (ICIs) have been approved to prolong overall survival (OS), compared to other treatments. However, the recent studies reported consistent and inconsistent results. Hence, we conducted this meta-analysis to evaluate the efficacy of ICIs. The articles were identified by searching PubMed, Embase, and Google Scholar published up to December 2021. A total of 12,126 participants (6,450 cases and 5,676 controls) were involved in the meta-analysis. Median OS and median progression-free survival (PFS) were selected to evaluate the efficacy of cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed cell death 1 (PD-1), and programmed death ligand 1 (PD-L1) inhibitors (ipilimumab, nivolumab or pembrolizumab, and atezolizumab, respectively). Utilizing the random-effect model, hazard ratios (HRs) with 95 confidence intervals (CIs) were calculated by R software. We observed a significant association between cancer patients and ICIs in OS (HR = 0.79, CI = 0.74-0.84) and PFS (HR = 0.80, CI = 0.75-0.86). The meta-analysis suggested that ICIs were associated with obvious improvements in PFS and OS compared with non-ICI therapies.
AbstractList IntroductionImmune checkpoint inhibitors (ICIs) have been approved to prolong overall survival (OS), compared to other treatments. However, the recent studies reported consistent and inconsistent results. Hence, we conducted this meta-analysis to evaluate the efficacy of ICIs.Materials and MethodsThe articles were identified by searching PubMed, Embase, and Google Scholar published up to December 2021. A total of 12,126 participants (6,450 cases and 5,676 controls) were involved in the meta-analysis. Median OS and median progression-free survival (PFS) were selected to evaluate the efficacy of cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed cell death 1 (PD-1), and programmed death ligand 1 (PD-L1) inhibitors (ipilimumab, nivolumab or pembrolizumab, and atezolizumab, respectively). Utilizing the random-effect model, hazard ratios (HRs) with 95 confidence intervals (CIs) were calculated by R software.ResultsWe observed a significant association between cancer patients and ICIs in OS (HR = 0.79, CI = 0.74–0.84) and PFS (HR = 0.80, CI = 0.75–0.86).ConclusionsThe meta-analysis suggested that ICIs were associated with obvious improvements in PFS and OS compared with non-ICI therapies.
Immune checkpoint inhibitors (ICIs) have been approved to prolong overall survival (OS), compared to other treatments. However, the recent studies reported consistent and inconsistent results. Hence, we conducted this meta-analysis to evaluate the efficacy of ICIs.IntroductionImmune checkpoint inhibitors (ICIs) have been approved to prolong overall survival (OS), compared to other treatments. However, the recent studies reported consistent and inconsistent results. Hence, we conducted this meta-analysis to evaluate the efficacy of ICIs.The articles were identified by searching PubMed, Embase, and Google Scholar published up to December 2021. A total of 12,126 participants (6,450 cases and 5,676 controls) were involved in the meta-analysis. Median OS and median progression-free survival (PFS) were selected to evaluate the efficacy of cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed cell death 1 (PD-1), and programmed death ligand 1 (PD-L1) inhibitors (ipilimumab, nivolumab or pembrolizumab, and atezolizumab, respectively). Utilizing the random-effect model, hazard ratios (HRs) with 95 confidence intervals (CIs) were calculated by R software.Materials and MethodsThe articles were identified by searching PubMed, Embase, and Google Scholar published up to December 2021. A total of 12,126 participants (6,450 cases and 5,676 controls) were involved in the meta-analysis. Median OS and median progression-free survival (PFS) were selected to evaluate the efficacy of cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed cell death 1 (PD-1), and programmed death ligand 1 (PD-L1) inhibitors (ipilimumab, nivolumab or pembrolizumab, and atezolizumab, respectively). Utilizing the random-effect model, hazard ratios (HRs) with 95 confidence intervals (CIs) were calculated by R software.We observed a significant association between cancer patients and ICIs in OS (HR = 0.79, CI = 0.74-0.84) and PFS (HR = 0.80, CI = 0.75-0.86).ResultsWe observed a significant association between cancer patients and ICIs in OS (HR = 0.79, CI = 0.74-0.84) and PFS (HR = 0.80, CI = 0.75-0.86).The meta-analysis suggested that ICIs were associated with obvious improvements in PFS and OS compared with non-ICI therapies.ConclusionsThe meta-analysis suggested that ICIs were associated with obvious improvements in PFS and OS compared with non-ICI therapies.
Immune checkpoint inhibitors (ICIs) have been approved to prolong overall survival (OS), compared to other treatments. However, the recent studies reported consistent and inconsistent results. Hence, we conducted this meta-analysis to evaluate the efficacy of ICIs. The articles were identified by searching PubMed, Embase, and Google Scholar published up to December 2021. A total of 12,126 participants (6,450 cases and 5,676 controls) were involved in the meta-analysis. Median OS and median progression-free survival (PFS) were selected to evaluate the efficacy of cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed cell death 1 (PD-1), and programmed death ligand 1 (PD-L1) inhibitors (ipilimumab, nivolumab or pembrolizumab, and atezolizumab, respectively). Utilizing the random-effect model, hazard ratios (HRs) with 95 confidence intervals (CIs) were calculated by R software. We observed a significant association between cancer patients and ICIs in OS (HR = 0.79, CI = 0.74-0.84) and PFS (HR = 0.80, CI = 0.75-0.86). The meta-analysis suggested that ICIs were associated with obvious improvements in PFS and OS compared with non-ICI therapies.
Author Xu, Li
Yan, Xin
Ding, Weiyue
AuthorAffiliation 1 College of Computer Science and Technology, Harbin Engineering University , Harbin , China
3 School of Mathematics, Harbin Institute of Technology , Harbin , China
2 Key Laboratory of Symbolic Computation and Knowledge Engineering of Ministry of Education, Jilin University , Changchun , China
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Keywords programmed cell death 1
cytotoxic T-lymphocyte-associated protein 4
progression-free survival
meta-analysis
overall survival
programmed death ligand 1
immune checkpoint inhibitors
Language English
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This article was submitted to Cancer Genetics, a section of the journal Frontiers in Oncology
Edited by: Liang Cheng, Harbin Medical University, China
Reviewed by: Xiangtao Li, Jilin University, China; Yang Yu, Shenyang Normal University, China
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Snippet Immune checkpoint inhibitors (ICIs) have been approved to prolong overall survival (OS), compared to other treatments. However, the recent studies reported...
IntroductionImmune checkpoint inhibitors (ICIs) have been approved to prolong overall survival (OS), compared to other treatments. However, the recent studies...
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SubjectTerms cytotoxic T-lymphocyte-associated protein 4
immune checkpoint inhibitors
meta-analysis
Oncology
overall survival
programmed cell death 1
progression-free survival
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Title Meta-Analysis of Efficacy From CTLA-4 and PD-1/PD-L1 Inhibitors in Cancer Patients
URI https://www.ncbi.nlm.nih.gov/pubmed/35574317
https://www.proquest.com/docview/2665106003
https://pubmed.ncbi.nlm.nih.gov/PMC9097585
https://doaj.org/article/47d95bbee3eb4cd2aa55f2e9f791fe33
Volume 12
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