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 in | Frontiers in oncology Vol. 12; p. 876098 |
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Language | English |
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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. |
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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 |
AuthorAffiliation_xml | – name: 1 College of Computer Science and Technology, Harbin Engineering University , Harbin , China – name: 3 School of Mathematics, Harbin Institute of Technology , Harbin , China – name: 2 Key Laboratory of Symbolic Computation and Knowledge Engineering of Ministry of Education, Jilin University , Changchun , China |
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CitedBy_id | crossref_primary_10_3389_fonc_2023_1160824 crossref_primary_10_3390_cancers14215289 crossref_primary_10_1631_jzus_B2300492 |
Cites_doi | 10.1001/jamanetworkopen.2021.7728 10.1016/S0140-6736(16)00587-0 10.1056/NEJMoa1104621 10.2307/2533446 10.1136/bmj.315.7109.629 10.3322/caac.21660 10.1093/annonc/mdz453.004 10.1016/S1470-2045(15)70076-8 10.1016/S0140-6736(15)01281-7 10.1016/S0140-6736(16)32517-X 10.1200/JCO.2016.71.8023 10.1016/S1470-2045(14)70189-5 10.1634/theoncologist.2015-0507 10.1158/2326-6066.CIR-16-0237 10.1093/annonc/mds213 10.1200/JCO.2016.67.6601 10.1002/cpt.394 10.1056/NEJMoa1507643 10.1016/j.it.2019.02.002 10.1056/NEJMoa1504627 10.1056/NEJMoa1003466 10.1016/j.annonc.2021.01.071 10.1016/S0140-6736(20)30230-0 10.1200/JCO.2016.69.1584 10.1093/annonc/mdz094 10.1038/471561a 10.1056/NEJMoa1613683 10.1111/cas.15059 10.1016/S1470-2045(15)00083-2 10.1200/JCO.20.00793 10.1158/1078-0432.CCR-16-0712 10.1515/hmbci-2017-0022 10.1186/s13045-016-0277-y |
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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 |
License | Copyright © 2022 Xu, Yan and Ding. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 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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Title | Meta-Analysis of Efficacy From CTLA-4 and PD-1/PD-L1 Inhibitors in Cancer Patients |
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