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


Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
04 2021
Historique:
received: 18 07 2020
revised: 27 10 2020
accepted: 30 10 2020
pubmed: 15 12 2020
medline: 10 8 2021
entrez: 14 12 2020
Statut: ppublish

Résumé

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. 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. 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). 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.

Sections du résumé

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.

Identifiants

pubmed: 33309564
pii: S1558-7673(20)30248-2
doi: 10.1016/j.clgc.2020.10.006
pii:
doi:

Substances chimiques

Cisplatin Q20Q21Q62J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

125-134

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Olivia A Do (OA)

School of Medicine, University of Washington School of Medicine, Seattle, WA.

Lorin A Ferris (LA)

School of Medicine, University of Washington School of Medicine, Seattle, WA.

Sarah K Holt (SK)

Department of Urology, University of Washington Medical Center, Seattle, WA.

Jorge D Ramos (JD)

Seagen Inc, Bothell, WA.

Lauren C Harshman (LC)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.

Elizabeth R Plimack (ER)

Division of Genitourinary Medical Oncology, Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA.

Simon J Crabb (SJ)

University of Southampton, Clinical Trials Unit, MP131, Southampton General Hospital, Southampton, Hants, United Kingdom.

Sumanta K Pal (SK)

Department of Medical Oncology & Therapeutics Research, City of Hope Comprehensive Cancer Center, Duarte, CA.

Ugo De Giorgi (U)

Department of Medical Oncology, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola FC, Italy.

Sylvain Ladoire (S)

Georges Francois Leclerc Cancer Center INSERM U1231, Dijon, France.

Jack Baniel (J)

Department of Urology, Rabin Medical Center, Tel Aviv University, Petah Tikva, Israel.

Andrea Necchi (A)

Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.

Ulka N Vaishampayan (UN)

Department of Internal Medicine/Oncology, University of Michigan, Ann Arbor, MI.

Aristotelis Bamias (A)

Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece.

Joaquim Bellmunt (J)

Department of Medical Oncology, Beth Israel Deaconess Medical Center, Boston, MA.

Sandy Srinivas (S)

Department of Medicine/Oncology, Stanford Cancer Institute, Palo Alto, CA.

Tanya B Dorff (TB)

Department of Medical Oncology & Therapeutics Research, City of Hope Comprehensive Cancer Center, Duarte, CA.

Matt D Galsky (MD)

Department of Medicine, Division of Oncology, Mount Sinai Hospital, New York, NY.

Evan Y Yu (EY)

Division of Oncology, Department of Medicine, University of Washington, Seattle Cancer Care Alliance, Seattle, WA. Electronic address: evanyu@uw.edu.

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