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Randomized phase III KEYNOTE-045 trial of pembrolizumab versus paclitaxel, docetaxel, or vinflunine in recurrent advanced urothelial cancer: results of >2 years of follow-up

Authors :
Lawrence Fong
Yves Fradet
Winald R. Gerritsen
David I. Quinn
David J. Vaughn
Daniel P. Petrylak
Joaquim Bellmunt
Howard Gurney
Dean F. Bajorin
R. de Wit
Stéphane Culine
Toni K. Choueiri
J.-L. Lee
Miguel Angel Climent
N. J. Vogelzang
Tara L. Frenkl
Andrea Necchi
Kijoeng Nam
Cora N. Sternberg
Rodolfo F. Perini
Medical Oncology
Fradet, Y
Bellmunt, J
Vaughn, Dj
Lee, Jl
Fong, L
Vogelzang, Nj
Climent, Ma
Petrylak, Dp
Choueiri, Tk
Necchi, A
Gerritsen, W
Gurney, H
Quinn, Di
Culine, S
Sternberg, Cn
Nam, K
Frenkl, Tl
Perini, Rf
de Wit, R
Bajorin, Df
Source :
Annals of oncology : official journal of the European Society for Medical Oncology, vol 30, iss 6, Annals of Oncology, Annals of Oncology, 30(6), 970-976. Elsevier Ltd., Annals of Oncology, 30, 6, pp. 970-976, Annals of Oncology, 30, 970-976
Publication Year :
2019
Publisher :
eScholarship, University of California, 2019.

Abstract

Background Novel second-line treatments are needed for patients with advanced urothelial cancer (UC). Interim analysis of the phase III KEYNOTE-045 study showed a superior overall survival (OS) benefit of pembrolizumab, a programmed death 1 inhibitor, versus chemotherapy in patients with advanced UC that progressed on platinum-based chemotherapy. Here we report the long-term safety and efficacy outcomes of KEYNOTE-045. Patients and methods Adult patients with histologically/cytologically confirmed UC whose disease progressed after first-line, platinum-containing chemotherapy were enrolled. Patients were randomly assigned 1 : 1 to receive pembrolizumab [200 mg every 3 weeks (Q3W)] or investigator's choice of paclitaxel (175 mg/m2 Q3W), docetaxel (75 mg/m2 Q3W), or vinflunine (320 mg/m2 Q3W). Primary end points were OS and progression-free survival (PFS) per Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST v1.1) by blinded independent central radiology review (BICR). A key secondary end point was objective response rate per RECIST v1.1 by BICR. Results A total of 542 patients were enrolled (pembrolizumab, n = 270; chemotherapy, n = 272). Median follow-up as of 26 October 2017 was 27.7 months. Median 1- and 2-year OS rates were higher with pembrolizumab (44.2% and 26.9%, respectively) than chemotherapy (29.8% and 14.3%, respectively). PFS rates did not differ between treatment arms; however, 1- and 2-year PFS rates were higher with pembrolizumab. The objective response rate was also higher with pembrolizumab (21.1% versus 11.0%). Median duration of response to pembrolizumab was not reached (range 1.6+ to 30.0+ months) versus chemotherapy (4.4 months; range 1.4+ to 29.9+ months). Pembrolizumab had lower rates of any grade (62.0% versus 90.6%) and grade ≥3 (16.5% versus 50.2%) treatment-related adverse events than chemotherapy. Conclusions Long-term results (>2 years' follow-up) were consistent with those of previously reported analyses, demonstrating continued clinical benefit of pembrolizumab over chemotherapy for efficacy and safety for treatment of locally advanced/metastatic, platinum-refractory UC. Trial registration ClinicalTrials.gov: NCT02256436.

Details

ISSN :
02256436 and 09237534
Database :
OpenAIRE
Journal :
Annals of oncology : official journal of the European Society for Medical Oncology, vol 30, iss 6, Annals of Oncology, Annals of Oncology, 30(6), 970-976. Elsevier Ltd., Annals of Oncology, 30, 6, pp. 970-976, Annals of Oncology, 30, 970-976
Accession number :
edsair.doi.dedup.....4a4a787c095cc0fd203a7dd10ec701e7