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Efficacy of PD-1 & PD-L1 inhibitors in older adults: a meta-analysis
BACKGROUND: Immune checkpoint inhibitors targeting PD-1/PD-L1 pathway demonstrated promising activities in variety of malignancies, however little is known regarding their efficacy in adults aged ≥65 years. METHODS: We conducted a systematic review and a study-level meta-analysis to explore efficacy...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885356/ https://www.ncbi.nlm.nih.gov/pubmed/29618381 http://dx.doi.org/10.1186/s40425-018-0336-8 |
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author | Elias, Rawad Giobbie-Hurder, Anita McCleary, Nadine Jackson Ott, Patrick Hodi, F. Stephen Rahma, Osama |
author_facet | Elias, Rawad Giobbie-Hurder, Anita McCleary, Nadine Jackson Ott, Patrick Hodi, F. Stephen Rahma, Osama |
author_sort | Elias, Rawad |
collection | PubMed |
description | BACKGROUND: Immune checkpoint inhibitors targeting PD-1/PD-L1 pathway demonstrated promising activities in variety of malignancies, however little is known regarding their efficacy in adults aged ≥65 years. METHODS: We conducted a systematic review and a study-level meta-analysis to explore efficacy of ICIs based on age, younger vs older than 65 years. We included in this analysis randomized controlled phase II or III studies in patients with metastatic solid tumors that compared efficacy of PD-1 or PD-L1 inhibitors to a non-PD-1/PD-L1 inhibitor. Aggregated estimates of overall survival (OS) and progression-free survival (PFS) are based on random/mixed effects (RE) models to allow for heterogeneity between the studies. RESULTS: Initial search identified 53 articles, 17 were randomized controlled trials that compared nivolumab, pembrolizumab or atezolizumab to chemotherapy or targeted therapy. Only 9 trials reported hazard ratiios (HR) for OS based on age and were included in this meta-analysis. Out of those studies seven reported HR for PFS but only 4 studies included subgroup-analysis based on age for PFS. The overall estimated random-effects HR for death was 0.64 with 95% CI of 0.54–0.76 in patients ≥65 years vs. 0.68 with 95% CI of 0.61–0.75 in patients < 65 years. The overall estimated random-effects for HR for progression was 0.74 with 95% CI of 0.60–0.92 in patients ≥65 years vs. 0.73 with 95% CI of 0.61–0.88 in patients < 65 years. CONCLUSIONS: PD-1 (nivolumab and pembrolizumab) and PD-L1 (atezolizumab) inhibitors had comparable efficacy in adults younger vs ≥ 65 years. |
format | Online Article Text |
id | pubmed-5885356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58853562018-04-09 Efficacy of PD-1 & PD-L1 inhibitors in older adults: a meta-analysis Elias, Rawad Giobbie-Hurder, Anita McCleary, Nadine Jackson Ott, Patrick Hodi, F. Stephen Rahma, Osama J Immunother Cancer Research Article BACKGROUND: Immune checkpoint inhibitors targeting PD-1/PD-L1 pathway demonstrated promising activities in variety of malignancies, however little is known regarding their efficacy in adults aged ≥65 years. METHODS: We conducted a systematic review and a study-level meta-analysis to explore efficacy of ICIs based on age, younger vs older than 65 years. We included in this analysis randomized controlled phase II or III studies in patients with metastatic solid tumors that compared efficacy of PD-1 or PD-L1 inhibitors to a non-PD-1/PD-L1 inhibitor. Aggregated estimates of overall survival (OS) and progression-free survival (PFS) are based on random/mixed effects (RE) models to allow for heterogeneity between the studies. RESULTS: Initial search identified 53 articles, 17 were randomized controlled trials that compared nivolumab, pembrolizumab or atezolizumab to chemotherapy or targeted therapy. Only 9 trials reported hazard ratiios (HR) for OS based on age and were included in this meta-analysis. Out of those studies seven reported HR for PFS but only 4 studies included subgroup-analysis based on age for PFS. The overall estimated random-effects HR for death was 0.64 with 95% CI of 0.54–0.76 in patients ≥65 years vs. 0.68 with 95% CI of 0.61–0.75 in patients < 65 years. The overall estimated random-effects for HR for progression was 0.74 with 95% CI of 0.60–0.92 in patients ≥65 years vs. 0.73 with 95% CI of 0.61–0.88 in patients < 65 years. CONCLUSIONS: PD-1 (nivolumab and pembrolizumab) and PD-L1 (atezolizumab) inhibitors had comparable efficacy in adults younger vs ≥ 65 years. BioMed Central 2018-04-04 /pmc/articles/PMC5885356/ /pubmed/29618381 http://dx.doi.org/10.1186/s40425-018-0336-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Elias, Rawad Giobbie-Hurder, Anita McCleary, Nadine Jackson Ott, Patrick Hodi, F. Stephen Rahma, Osama Efficacy of PD-1 & PD-L1 inhibitors in older adults: a meta-analysis |
title | Efficacy of PD-1 & PD-L1 inhibitors in older adults: a meta-analysis |
title_full | Efficacy of PD-1 & PD-L1 inhibitors in older adults: a meta-analysis |
title_fullStr | Efficacy of PD-1 & PD-L1 inhibitors in older adults: a meta-analysis |
title_full_unstemmed | Efficacy of PD-1 & PD-L1 inhibitors in older adults: a meta-analysis |
title_short | Efficacy of PD-1 & PD-L1 inhibitors in older adults: a meta-analysis |
title_sort | efficacy of pd-1 & pd-l1 inhibitors in older adults: a meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885356/ https://www.ncbi.nlm.nih.gov/pubmed/29618381 http://dx.doi.org/10.1186/s40425-018-0336-8 |
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