Treatment of Metastatic Urothelial Carcinoma After Previous Cisplatin-based Chemotherapy for Localized Disease: A Retrospective Comparison of Different Chemotherapy Regimens

Olivia A. Do, Lorin A. Ferris, Sarah K. Holt, Jorge D. Ramos, Lauren C. Harshman, Elizabeth R. Plimack, Simon J. Crabb, Sumanta K. Pal, Ugo De Giorgi, Sylvain Ladoire, Jack Baniel, Andrea Necchi, Ulka N. Vaishampayan, Aristotelis Bamias, Joaquim Bellmunt, Sandy Srinivas, Tanya B. Dorff, Matt D. Galsky, Evan Y. Yu*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Background: Optimal chemotherapy for patients who received cisplatin for localized urothelial carcinoma (UC) and develop metastatic disease is unclear. We compared the efficacy of platinum-based (PBC) versus non–platinum-based (NPBC) first-line chemotherapy for metastasis. Patients and Methods: Data were collected from the Retrospective International Study of Cancers of the Urothelial Tract (RISC), a database of 3024 patients from 28 international academic centers from 2005 to 2012. Patient inclusion criteria included: (1) predominant UC; (2) any primary tumor site; (3) cT2-4, cN0-N2, cM0; (4) prior receipt of perioperative/radiation cisplatin-containing chemotherapy; and (5) receipt of cytotoxic chemotherapy in the first-line metastatic setting. Multivariate Cox proportional hazards models were used to show progression-free survival (PFS) and overall survival (OS) from the first day of chemotherapy for metastatic disease to date of censor. Results: Eligibility criteria was met by 132 patients (n = 74 PBC; n = 58 NPBC). The median OS was 8.13 months (interquartile range, 4.87-16.64 months) and 8.77 months (interquartile range, 4.01-13.49 months) for PBC and NPBC, respectively. Neither OS (hazard ratio [HR], 1.04; 95% confidence interval [CI], 0.64-1.69; P =.87) nor PFS (HR, 0.86; 95% CI, 0.56-1.31; P =.48) differed for PBC versus NPBC. However, for patients who received chemotherapy more than a year after perioperative/radiation chemotherapy, OS was superior for PBC over NPBC (HR, 0.31; 95% CI, 0.10-0.92; P =.03). Conclusions: There is no significant outcome difference between PBC and NPBC in patients with metastatic UC who previously received cisplatin-based chemotherapy for localized disease. However, if over a year has elapsed, return to PBC is associated with superior OS.

Original languageEnglish
Pages (from-to)125-134
Number of pages10
JournalClinical Genitourinary Cancer
Volume19
Issue number2
DOIs
StatePublished - Apr 2021

Funding

FundersFunder number
Ology Medical Education
Rainier Therapeutics
Sinai Icahn School of Medicine, NCCN
Sotio
Bristol-Myers Squibb
Pfizer
Astellas Pharma US
AstraZeneca14/588,503
Bayer
Genentech
Merck
Novartis
Roche
American Society of Clinical Oncology
AbbVie
Meso Scale Diagnostics
University of Michigan
Icahn School of Medicine at Mount Sinai20120322792
Takeda Pharmaceuticals U.S.A.
Janssen Pharmaceuticals
Merck Sharp and Dohme
Exelixis
Ipsen Biopharmaceuticals
Clovis Oncology
Myriad Genetics
Incyte
Advanced Accelerator Applications
Eisai
Agricultural University of Athens

    Keywords

    • Bladder cancer
    • First-line
    • Neoadjuvant
    • Platinum
    • Survival

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