@article{de3b749257f84412af82463cf151f18c,
title = "The Predictive and Prognostic Nature of Programmed Death-Ligand 1 in Malignant Pleural Mesothelioma: A Systematic Literature Review",
abstract = "Introduction: Given the emergence of combination of programmed cell death protein-1 and CTLA4 pathway blockade as effective treatment options in malignant pleural mesothelioma (MPM), there is interest in the extent to which programmed death-ligand 1 (PD-L1) expression may be prognostic of clinical outcomes and predictive of response to anti–programmed death (ligand) 1 (PD-[L]1) therapies. Methods: MEDLINE and EMBASE electronic databases were searched until November 4, 2020. English-language randomized trials and observational studies that reported clinical outcomes and PD-L1 expression in adult patients (>18 or >20 y) with MPM were included. Forest plots were used to descriptively summarize clinical outcome data across studies. Results: A total of 29 publications were identified providing data on the research question. Among the studies in which anti–PD-(L)1 therapies were not specified to have been used, 63% (10 of 16) found patients with tumors expressing PD-L1 (typically >1%) to have poorer survival than those with tumors expressing lower levels of PD-L1. Among the studies in which anti–PD-(L)1 therapies were used, 83% (five of six) did not reveal an association between survival and PD-L1 tumor expression. The single study directly comparing outcomes between those treated and untreated with anti–PD-(L)1 therapies across different PD-L1 cutoffs did not identify any differences between the groups. Conclusions: The quality and consistency of the existing evidence base are currently insufficient to draw conclusions regarding a prognostic or predictive role of PD-L1 in MPM. Furthermore, high-quality studies on this topic are required to support the use of PD-L1 as a biomarker in MPM.",
keywords = "Biomarker, Mesothelioma, PD-L1, Predictive, Prognostic",
author = "Mansfield, {Aaron S.} and Brown, {Rebecca J.} and Cormac Sammon and Daumont, {Melinda J.} and Mike McKenna and Sanzari, {Jenine K.} and Forde, {Patrick M.}",
note = "Funding Information: Disclosure: Dr. Mansfield reports receiving research support from Novartis and Verily; having remuneration to his institution for participation on advisory boards for AbbVie, AstraZeneca, Bristol-Myers Squibb, Genentech, and Janssen; receiving travel support and payment from Shanghai Roche Pharmaceuticals Ltd; and being a nonremunerated director of the Mesothelioma Applied Research Foundation. Drs. Brown and Sammon are full-time employees at PHMR. PHMR received financial support from Bristol-Myers Squibb for the work, including the development of the literature review and preparation of the manuscript. Dr. Daumont is a full-time employee of Bristol-Myers Squibb and owns stock in Bristol-Myers Squibb. Mr. McKenna{\textquoteright}s company provides consultancy services to Bristol-Myers Squibb. Dr. Sanzari is an employee of Bristol-Myers Squibb. Dr. Forde reports receiving research funding to his institution from AstraZeneca , Bristol-Myers Squibb , Corvus, and Novartis; serving as a consultant for Amgen , AstraZeneca , Bristol-Myers Squibb , Daiichi, G1 Therapeutics, Genentech , Iteos, Janssen, Novartis , Sanofi , and Surface; serving as a DSMB member for Polaris and Flame; and being a nonremunerated director of the Mesothelioma Applied Research Foundation. Funding Information: Disclosure: Dr. Mansfield reports receiving research support from Novartis and Verily; having remuneration to his institution for participation on advisory boards for AbbVie, AstraZeneca, Bristol-Myers Squibb, Genentech, and Janssen; receiving travel support and payment from Shanghai Roche Pharmaceuticals Ltd; and being a nonremunerated director of the Mesothelioma Applied Research Foundation. Drs. Brown and Sammon are full-time employees at PHMR. PHMR received financial support from Bristol-Myers Squibb for the work, including the development of the literature review and preparation of the manuscript. Dr. Daumont is a full-time employee of Bristol-Myers Squibb and owns stock in Bristol-Myers Squibb. Mr. McKenna's company provides consultancy services to Bristol-Myers Squibb. Dr. Sanzari is an employee of Bristol-Myers Squibb. Dr. Forde reports receiving research funding to his institution from AstraZeneca, Bristol-Myers Squibb, Corvus, and Novartis; serving as a consultant for Amgen, AstraZeneca, Bristol-Myers Squibb, Daiichi, G1 Therapeutics, Genentech, Iteos, Janssen, Novartis, Sanofi, and Surface; serving as a DSMB member for Polaris and Flame; and being a nonremunerated director of the Mesothelioma Applied Research Foundation. Publisher Copyright: {\textcopyright} 2022 The Authors",
year = "2022",
month = may,
doi = "10.1016/j.jtocrr.2022.100315",
language = "English (US)",
volume = "3",
journal = "JTO Clinical and Research Reports",
issn = "2666-3643",
publisher = "Elsevier Inc.",
number = "5",
}