Comparative Effectiveness of Immune Checkpoint Inhibitors in Patients with Platinum-Refractory Advanced Urothelial Carcinoma.
J Urol. 2020 Oct 20;:101097JU0000000000001412
Authors: Swami U, Haaland B, Kessel A, Nussenzveig R, Louis Maughan B, Esther J, Sirohi D, Pal SK, Grivas P, Agarwal N
Abstract
PURPOSE: Five programmed cell death protein 1 (PD-1) or its ligand (L1) inhibitors are approved for treatment of platinum-refractory locally advanced/unresectable or metastatic urothelial carcinoma. However, their comparative effectiveness is unknown. Herein we compared time to initiation of third therapy or death (TTTTD) and overall survival (OS) with different PD-1/L1 inhibitors in patients with platinum-refractory metastatic urothelial carcinoma.
METHODS: Patient-level data from a real-world de-identified database was extracted. Comparative effectiveness was inferred via Cox proportional hazards model, weighted by matching weights. Each patient's propensity for each treatment was modeled via random forest, based on potential drivers of treatment selection. A propensity score for each therapy was used to calculate a matching weight, targeting the same estimand as 1:1 matching of treatment groups with balance among potential confounders. Eligibility criteria included diagnosis of metastatic urothelial carcinoma, receipt of first-line treatment with a platinum-based chemotherapy, followed by initiation of single-agent PD-1/L1 inhibitor after disease progression from 8/1/2016 through 5/1/2019.
RESULTS: Overall 609 patients were eligible for analysis. Median TTTTD with atezolizumab, nivolumab, and pembrolizumab was 4.2, 5.3, and 4.5 months and median OS was 6.4, 8.0, and 8.3 months, respectively. Matching weighted analyses did not show strong evidence of differences among PD-1/L1 inhibitors in terms of TTTTD and OS.
CONCLUSIONS: In this large real-world cohort, effectiveness in terms of TTTTD and OS with PD-1/L1 inhibitors in patients with platinum-refractory locally advanced/unresectable or metastatic urothelial carcinoma was similar.
PMID: 33080152 [PubMed - as supplied by publisher]
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