In a phase II study reported in the Journal of Clinical Oncology, Matthew D. Galsky, MD, and colleagues found that maintenance pembrolizumab produced additional responses and improved progression-free survival vs placebo in patients with metastatic urothelial cancer who had at least stable disease on first-line platinum-based chemotherapy.
Matthew D. Galsky, MD
In the U.S. investigator-initiated double-blind trial, 108 patients with at least stable disease on first-line chemotherapy were randomly assigned between December 2015 and November 2018 to receive 200 mg of pembrolizumab once every 3 weeks (n = 55) or placebo (n = 53) for up to 24 months. Patients with disease progression on placebo could cross over to receive pembrolizumab. The primary outcome measure was progression-free survival.
Responses and Progression-Free Survival
Among 43 patients treated with pembrolizumab and 42 treated with placebo without complete response on chemotherapy, objective response was observed in 23% of those receiving pembrolizumab and 10% of those receiving placebo, including complete response in 9% vs 0%. Median progression-free survival was 5.4 months in the pembrolizumab group vs 3.0 months in the placebo group (hazard ratio [HR] = 0.65, P =.04).
Median overall survival was 22 months vs 18.7 months (HR = 0.91, 95% confidence interval = 0.52–1.59). Among 27 patients treated with placebo who crossed over to pembrolizumab after disease progression, the objective response rate was 22%, median progression-free survival after crossover was 2.7 months, and median overall survival after crossover was 15.8 months.
Among patients with available data, programmed cell death ligand 1 (PD-L1) combined positive score (CPS) was ≥ 10 in 30% of patients treated with pembrolizumab and 30% of patients treated with placebo. No significant interactions between PD-L1 CPS ≥ 10 and treatment group were observed for progression-free survival (P = .5) or overall survival (P = .9).
Grade 3 or 4 adverse events occurred in 59% of patients (grade 4 in 15%) of the pembrolizumab group vs 38% (all grade 3) of the placebo group. Immune-related adverse events requiring systemic steroid treatment occurred in 20% of patients initially randomly assigned to treatment with pembrolizumab. One patient in the pembrolizumab group died due to a treatment-related adverse event (hepatitis).
The investigators concluded, “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.”
Dr. Galsky, of Tisch Cancer Institute, Mount Sinai School of Medicine, is the corresponding author for the Journal of Clinical Oncology article.
Disclosure: The study was supported by Merck and by a National Cancer Institute grant to Tisch Cancer Institute Cancer Center. For full disclosures of the study authors, visit ascopubs.org.The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.