Programmed Death-1 or Programmed Death Ligand-1 Blockade in Patients with Platinum-resistant Metastatic Urothelial Cancer: A Systematic Review and Meta-analysis.


Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 01 02 2019
accepted: 23 05 2019
pubmed: 16 6 2019
medline: 18 12 2020
entrez: 16 6 2019
Statut: ppublish

Résumé

Several anti-programmed death-1 (anti-PD-1) and anti-programmed death ligand-1 (anti-PD-L1) antibodies have been approved by regulatory authorities for treatment of platinum-resistant metastatic urothelial cancer (mUC). The impact of these therapies on survival, and comparability of PD-1 versus PD-L1 blockade are unknown. To determine the restricted mean survival time (RMST) of patients with platinum-resistant mUC treated with PD-1/PD-L1 inhibitors and to compare RMSTs in patients treated with PD-1 versus PD-L1 inhibitors. We searched for phase 1, 2, and 3 clinical trials that assessed PD-1 or PD-L1 inhibition for patients with platinum-resistant mUC. Literature review and study selection, data abstraction, and risk of bias assessment were performed by two reviewers. Survival data were reconstructed using an algorithm that derives individual time-to-event data from published Kaplan-Meier curves. The RMST with 95% confidence interval (CIs) was calculated. From 836 references, six clinical trials were included. Survival data were reconstructed for 1315 and 736 patients treated with PD-1/PD-L1 inhibitors and chemotherapy, respectively. The RMSTs with PD-1/PD-L1 blockade up to 12 and 18mo of follow-up were 7.8mo (95% CI 7.6, 8.1) and 10mo (95% CI 9.7, 10.5), respectively. A network meta-analysis of two randomized trials revealed no significant difference in the RMST up to 18mo with PD-1 versus PD-L1 blockade (1.0mo; 95% CI -0.5, 2.3mo). Using reconstructed survival data from all six trials, the RMSTs with PD-1 versus PD-L1 blockade up to 12 and 18mo follow-up were 7.8mo (95% CI 7.7, 8.2) versus 7.8mo (95% CI 7.5, 8.2) and 10.1mo (95% CI 9.6, 10.7) versus 10mo (95% CI 9.5, 10.6), respectively. Our RMST estimates may be used as benchmarks to contextualize survival outcomes and inform future trial design with PD-1/PD-L1 inhibitors. PD-1 versus PD-L1 blockade in patients with mUC yields comparable survival outcomes. In this study, we found that outcomes for patients with metastatic bladder cancer treated with programmed death-1 and programmed death ligand-1 inhibitors, who received prior platinum-based chemotherapy, were similar.

Identifiants

pubmed: 31200951
pii: S0302-2838(19)30444-0
doi: 10.1016/j.eururo.2019.05.037
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
B7-H1 Antigen 0
CD274 protein, human 0
Platinum Compounds 0

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

782-789

Informations de copyright

Copyright © 2019 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Auteurs

Scot A Niglio (SA)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Rachel Jia (R)

Institute for Health Care Delivery Science, Population Health Science and Policy, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Jiayi Ji (J)

Institute for Health Care Delivery Science, Population Health Science and Policy, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Samuel Ruder (S)

Internal Medicine, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Vaibhav G Patel (VG)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Alberto Martini (A)

Urology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

John P Sfakianos (JP)

Urology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Kathryn E Marqueen (KE)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Nikhil Waingankar (N)

Urology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Reza Mehrazin (R)

Urology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Peter Wiklund (P)

Urology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Urology, Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden.

William K Oh (WK)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Madhu Mazumdar (M)

Institute for Health Care Delivery Science, Population Health Science and Policy, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Bart S Ferket (BS)

Institute for Health Care Delivery Science, Population Health Science and Policy, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Matthew D Galsky (MD)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Electronic address: matthew.galsky@mssm.edu.

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Classifications MeSH