@article{bdcf6e4d3ef3482a9247182c93edb7a2,
title = "Randomized Double-Blind Phase II Study of Maintenance Pembrolizumab Versus Placebo after First-Line Chemotherapy in Patients with Metastatic Urothelial Cancer",
abstract = "PURPOSE Platinum-based chemotherapy for first-line treatment of metastatic urothelial cancer is typically administered for a fixed duration followed by observation until progression. “Switch maintenance” therapy with PD-1 blockade at the time of chemotherapy cessation may be attractive for mechanistic and pragmatic reasons. PATIENTS AND METHODS Patients with metastatic urothelial cancer achieving at least stable disease on first-line platinum-based chemotherapy were enrolled. Patients were randomly assigned double-blind 1:1 to switch maintenance pembrolizumab 200 mg intravenously once every 3 weeks versus placebo for up to 24 months. Patients with disease progression on placebo could cross over to pembrolizumab. The primary objective was to determine the progression-free survival. Secondary objectives included determining overall survival as well as treatment outcomes according to PD-L1 combined positive score (CPS). RESULTS Between December 2015 and November 2018, 108 patients were randomly assigned to pembrolizumab (n 5 55) or placebo (n 5 53). The objective response rate was 23% with pembrolizumab and 10% with placebo. Treatment-emergent grade 3-4 adverse events occurred in 59% receiving pembrolizumab and 38% of patients receiving placebo. Progression-free survival was significantly longer with maintenance pembrolizumab versus placebo (5.4 months [95% CI, 3.1 to 7.3 months] v 3.0 months [95% CI; 2.7 to 5.5 months]; hazard ratio, 0.65; log-rank P 5 .04; maximum efficiency robust test P 5 .039). Median overall survival was 22 months (95% CI, 12.9 months to not reached) with pembrolizumab and 18.7 months (95% CI, 11.4 months to not reached) with placebo. There was no significant interaction between PD-L1 CPS $ 10 and treatment arm for progression-free survival or overall survival. CONCLUSION Switch maintenance pembrolizumab leads to additional objective responses in patients achieving at least stable disease with first-line platinum-based chemotherapy and prolongs progression-free survival in patients with metastatic urothelial cancer.",
author = "Galsky, {Matthew D.} and Amir Mortazavi and Milowsky, {Matthew I.} and Saby George and Sumati Gupta and Fleming, {Mark T.} and Dang, {Long H.} and Geynisman, {Daniel M.} and Radhika Walling and Alter, {Robert S.} and Mohamad Kassar and Jue Wang and Shilpa Gupta and Nancy Davis and Joel Picus and George Philips and Quinn, {David I.} and {Kenneth Haines}, G. and Hahn, {Noah M.} and Qianqian Zhao and Menggang Yu and Pal, {Sumanta K.}",
note = "Funding Information: Supported by Merck and by the Tisch Cancer Institute Cancer Center Grant No. P30 CA196521. Janssen Oncology (Inst), Dendreon (Inst), Novartis (Inst), Bristol-Myers Squibb (Inst), Merck (Inst), AstraZeneca (Inst), Genentech/Roche (Inst) Acerta Pharma (Inst), Genentech/Roche (Inst), Merck (Inst), Novartis (Inst), Seattle Genetics (Inst), Mirati Therapeutics (Inst), Bristol-Myers Squibb (Inst), Roche (Inst), Astellas Pharma (Inst) Merck (Inst), Acerta Pharma (Inst), Roche/Genentech (Inst), Bristol-Myers Squibb (Inst), Seattle Genetics (Inst), Astellas Pharma (Inst), Clovis Oncology (Inst), Inovio Pharmaceuticals (Inst), AstraZeneca (Inst), X4 Pharmaceuticals (Inst), Mirati Therapeutics (Inst), Boehringer Ingelheim (Inst), Constellation Pharmaceuticals (Inst), Jounce Therapeutics (Inst), Syndax (Inst), Innocrin Pharma (Inst), MedImmune (Inst), Cerulean Pharma (Inst), Incyte (Inst) Pfizer (Inst), Merck (Inst), Agensys (Inst), Novartis (Inst), Bristol-Myers Squibb (Inst), Bayer (Inst), Eisai (Inst), Seattle Genetics/Astellas (Inst), Calithera Biosciences (Inst), Immunomedics (Inst), Corvus Pharmaceuticals (Inst) Mirati Therapeutics (Inst), Novartis (Inst), Pfizer (Inst), Viralytics (Inst), Hoosier Cancer Research Network (Inst), Rexahn Pharmaceuticals (Inst), Five Prime Therapeutics (Inst), Incyte (Inst), MedImmune (Inst), Merck (Inst), Bristol-Myers Squibb (Inst), Clovis Oncology (Inst), LSK (Inst), QED (Inst) Genentech (Inst), Merck (Inst), Calithera Biosciences (Inst), Astellas Pharma (Inst) Astellas Medivation (Inst), Pfizer (Inst), MedImmune (Inst), Merck (Inst), Moderna Therapeutics (Inst), Bristol-Myers Squibb (Inst), Incyte (Inst) AstraZeneca (Inst), Hoffman-LaRoche (Inst), Pfizer (Inst), Merck (Inst), Incyte (Inst), Mirati Therapeutics (Inst), Seattle Genetics/Astellas (Inst), Calithera Biosciences (Inst), Taris BioMedical (Inst), Immunomedics (Inst), Bristol-Myers Squibb (Inst), Jounce Therapeutics (Inst), Exelixis (Inst) BioClin Therapeutics (Inst), Agensys (Inst), Mirati Therapeutics (Inst), Innocrin Pharma (Inst), Rexahn Pharmaceuticals (Inst), Endocyte (Inst), Seattle Genetics (Inst), BioClin Therapeutics (Inst), TRACON Pharma (Inst), eFFECTOR Therapeutics (Inst) Millennium (Inst), Genentech/Roche (Inst), Sanofi (Inst), GlaxoSmithKline (Inst), Merck (Inst), Pfizer (Inst) Genentech/Roche (Inst), Merck (Inst), Bristol-Myers Squibb (Inst), AstraZeneca/MedImmune (Inst), Principa Biopharma (Inst), Acerta Pharma (Inst), Incyte (Inst), Seattle Genetics/Astellas (Inst), Astex Pharmaceuticals (Inst), Pieris Pharmaceuticals (Inst) Medivation Funding Information: Supported by Merck and by the Tisch Cancer Institute Cancer Center Grant No. P30 CA196521. Publisher Copyright: {\textcopyright} 2020 by American Society of Clinical Oncology",
year = "2020",
month = apr,
day = "10",
doi = "10.1200/JCO.19.03091",
language = "English (US)",
volume = "38",
pages = "1797--1806",
journal = "Journal of Clinical Oncology",
issn = "0732-183X",
publisher = "American Society of Clinical Oncology",
number = "16",
}