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      Association of Sex, Age, and Eastern Cooperative Oncology Group Performance Status With Survival Benefit of Cancer Immunotherapy in Randomized Clinical Trials : A Systematic Review and Meta-analysis

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          Key Points

          Question

          Are different sex, age, and Eastern Cooperative Oncology Group performance status (0 vs ≥1) factors associated with the same benefit with immune checkpoint inhibitor immunotherapy compared with non–immune checkpoint inhibitor control therapy in the treatment of advanced cancers?

          Findings

          In this meta-analysis of 37 randomized clinical trials involving 23 760 patients, no evidence of a significant difference in overall survival benefit from immune checkpoint inhibitors over control therapy between patients with different sex, age, or Eastern Cooperative Oncology Group performance status was found.

          Meaning

          The results of this meta-analysis suggest that immunotherapy may confer a survival benefit in the treatment of advanced cancer regardless of patient sex, age, and performance status and should not be restricted based on these characteristics.

          Abstract

          Importance

          Sex, age, and Eastern Cooperative Oncology Group (ECOG) performance status (PS) may affect immune response. However, the association of these factors with the survival benefit of cancer immunotherapy with immune checkpoint inhibitors (ICIs) remains unclear.

          Objective

          To assess the potential sex, age, and ECOG PS differences of immunotherapy survival benefit in patients with advanced cancer.

          Data Sources

          PubMed, Web of Science, Embase, and Scopus were searched from inception to August 31, 2019.

          Study Selection

          Published randomized clinical trials comparing overall survival (OS) in patients with advanced cancer treated with ICI immunotherapy vs non-ICI control therapy were included.

          Data Extraction and Synthesis

          Pooled OS hazard ratio (HR) and 95% CI for patients of different sex, age (<65 and ≥65 years) or ECOG PS (0 and ≥1) were calculated separately using a random-effects model, and the heterogeneity between paired estimates was assessed using an interaction test by pooling study-specific interaction HRs. This study followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guideline.

          Main Outcomes and Measures

          The difference in survival benefit of ICIs between sex, age (<65 vs ≥65 years), and ECOG PS (0 vs ≥1), as well as the difference stratified by cancer type, line of therapy, agent of immunotherapy, and immunotherapy strategy in the intervention arm.

          Results

          Thirty-seven phase 2 or 3 randomized clinical trials involving 23 760 patients were included. An OS benefit of immunotherapy was found for both men (HR, 0.75; 95% CI, 0.71-0.81) and women (HR, 0.79; 95% CI, 0.72-0.88); for both younger (<65 years: HR, 0.77; 95% CI, 0.71-0.83) and older (≥65 years: HR, 0.78; 95% CI, 0.72-0.84) patients; and for both patients with ECOG PS 0 (HR, 0.81; 95% CI, 0.73-0.90) and PS greater than or equal to 1 (HR, 0.79; 95% CI, 0.74-0.84). No significant difference of relative benefit from immunotherapy over control therapy was found in patients of different sex ( P = .25, I 2  = 19.02%), age ( P = .94, I 2  = 15.57%), or ECOG PS ( P = .74, I 2  = 0%). No significant difference was found in subgroup analyses by cancer type, line of therapy, agent of immunotherapy, and immunotherapy strategy in the intervention arm.

          Conclusions and Relevance

          This meta-analysis found no evidence of an association of sex, age (<65 vs ≥65 years), or ECOG PS (0 vs ≥1) with cancer immunotherapy survival benefit. This finding suggests that the use of ICIs in advanced cancer should not be restricted to certain patients in sex, age, or ECOG PS categories.

          Abstract

          This meta-analysis examines the association of sex, age, and Eastern Cooperative Oncology Group performance status with overall survival in patients treated with immune checkpoint inhibitors for advanced cancer.

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          Most cited references16

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          • Abstract: found
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          Combined nivolumab and ipilimumab versus ipilimumab alone in patients with advanced melanoma: 2-year overall survival outcomes in a multicentre, randomised, controlled, phase 2 trial.

          Results from phase 2 and 3 trials in patients with advanced melanoma have shown significant improvements in the proportion of patients achieving an objective response and prolonged progression-free survival with the combination of nivolumab (an anti-PD-1 antibody) plus ipilimumab (an anti-CTLA-4 antibody) compared with ipilimumab alone. We report 2-year overall survival data from a randomised controlled trial assessing this treatment in previously untreated advanced melanoma.
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            Cancer immunotherapy efficacy and patients' sex: a systematic review and meta-analysis

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              Randomized, Double-Blind, Phase III Trial of Ipilimumab Versus Placebo in Asymptomatic or Minimally Symptomatic Patients With Metastatic Chemotherapy-Naive Castration-Resistant Prostate Cancer

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                Author and article information

                Journal
                JAMA Netw Open
                JAMA Netw Open
                JAMA Netw Open
                JAMA Network Open
                American Medical Association
                2574-3805
                7 August 2020
                August 2020
                7 August 2020
                : 3
                : 8
                : e2012534
                Affiliations
                [1 ]The Comprehensive Cancer Center of Drum Tower Hospital, Clinical Cancer Institute of Nanjing University, Nanjing, China
                [2 ]Division of Medical Oncology, Mayo Clinic, Rochester, Minnesota
                [3 ]Division of Hematology, Mayo Clinic, Rochester, Minnesota
                [4 ]Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston
                Author notes
                Article Information
                Accepted for Publication: May 16, 2020.
                Published: August 7, 2020. doi:10.1001/jamanetworkopen.2020.12534
                Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2020 Yang F et al. JAMA Network Open.
                Corresponding Author: Yucai Wang, MD, PhD, Division of Hematology, Mayo Clinic, 200 First St SW, Rochester, MN 55905 ( wang.yucai@ 123456mayo.edu ).
                Author Contributions: Drs Yang and Y. Wang had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
                Concept and design: Yang, Molina, Chintakuntlawar, Wei, Liu, M. L. Wang, Y. Wang.
                Acquisition, analysis, or interpretation of data: Yang, Markovic, Molina, Halfdanarson, Pagliaro, Li, L. Wang, Nowakowski, M. L. Wang, Y. Wang.
                Drafting of the manuscript: Yang, Chintakuntlawar, M. L. Wang, Y. Wang.
                Critical revision of the manuscript for important intellectual content: All authors.
                Statistical analysis: Yang, Y. Wang.
                Administrative, technical, or material support: Yang, Halfdanarson, Nowakowski, M. L. Wang, Y. Wang.
                Supervision: Yang, Molina, Halfdanarson, Chintakuntlawar, Wei, Liu, M. L. Wang, Y. Wang.
                Conflict of Interest Disclosures: Dr Halfdanarson reported receiving personal fees from Curium, Terumo, Lexicon, and ScioScientific; serving as a consult or on an advisory board without personal compensation from Advanced Accelerator Applications and Ipsen; and receiving grants from Ipsen, Thermo Fisher Scientific, and Basilea outside the submitted work. Dr M. L. Wang reported receiving grants, personal fees, and nonfinancial support from Janssen, AstraZeneca, Acerta Pharma, Pharmacyclics, Kite Pharma, Celgene, and Loxo Oncology; grants and nonfinancial support from VelosBio, BeiGene, BioInvent, and Verastem; grants from Eli Lilly and Aviara; personal fees and nonfinancial support from Juno Therapeutics; and personal fees from Guidepoint Global and Pulse Biosciences outside the submitted work. No other disclosures were reported.
                Article
                zoi200474
                10.1001/jamanetworkopen.2020.12534
                7414387
                32766800
                5725a4cc-1923-43c8-a5cf-214e0095b133
                Copyright 2020 Yang F et al. JAMA Network Open.

                This is an open access article distributed under the terms of the CC-BY License.

                History
                : 12 November 2019
                : 16 May 2020
                Categories
                Research
                Original Investigation
                Online Only
                Oncology

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