Efficacy of Platinum Rechallenge in Metastatic Urothelial Carcinoma After Previous Platinum-Based Chemotherapy for Metastatic Disease.

Antineoplastic agents Cisplatin Drug therapy Platinum compounds Urinary bladder neoplasms Urologic neoplasms carboplatin combination

Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
12 2021
Historique:
received: 20 04 2021
accepted: 23 07 2021
pubmed: 7 8 2021
medline: 22 12 2021
entrez: 6 8 2021
Statut: ppublish

Résumé

Fit patients with metastatic urothelial carcinoma (mUC) receive first-line platinum-based combination chemotherapy (fPBC) as standard of care and may receive additional later-line chemotherapy after progression. Our study compares outcomes with subsequent platinum-based chemotherapy (sPBC) versus subsequent non-platinum-based chemotherapy (sNPBC). Patients from 27 international centers in the Retrospective International Study of Cancers of the Urothelium (RISC) who received fPBC for mUC and at least two cycles of subsequent chemotherapy were included in this study. A multivariable Cox proportional hazards model compared overall survival (OS) and progression-free survival (PFS). One hundred thirty-five patients received sPBC and 161 received sNPBC. Baseline characteristics were similar between groups, except patients who received sPBC had higher baseline hemoglobin, higher disease control rate with fPBC, and longer time since fPBC. OS was superior in the sPBC group (median 7.9 vs 5.5 months) in a model adjusting for comorbidity burden, performance status, liver metastases, number of fPBC cycles received, best response to fPBC, and time since fPBC (hazard ratio, 0.72; 95% confidence interval, 0.53-0.98; p = .035). There was no difference in PFS. More patients in the sPBC group achieved disease control than in the sNPBC group (57.4% vs 44.8%; p = .041). Factors associated with achieving disease control in the sPBC group but not the sNPBC group included longer time since fPBC, achieving disease control with fPBC, and absence of liver metastases. After receiving fPBC for mUC, patients who received sPBC had better OS and disease control. This may help inform the choice of subsequent chemotherapy in patients with mUC. Patients with progressive metastatic urothelial carcinoma after first-line platinum-based combination chemotherapy may now receive immuno-oncology agents, erdafitinib, enfortumab vedotin, or sacituzumab govitecan-hziy; however, those ineligible for these later-line therapies or who progress after receiving them may be considered for subsequent chemotherapy. In this retrospective study of 296 patients, survival outcomes and disease control rates were better in those receiving subsequent platinum-based rechallenge compared with non-platinum-based chemotherapy, suggesting that patients should receive platinum rechallenge if clinically able. Disease control with platinum rechallenge was more likely with prior first-line platinum having achieved disease control, longer time since first-line platinum, and absence of liver metastases.

Sections du résumé

BACKGROUND
Fit patients with metastatic urothelial carcinoma (mUC) receive first-line platinum-based combination chemotherapy (fPBC) as standard of care and may receive additional later-line chemotherapy after progression. Our study compares outcomes with subsequent platinum-based chemotherapy (sPBC) versus subsequent non-platinum-based chemotherapy (sNPBC).
MATERIALS AND METHODS
Patients from 27 international centers in the Retrospective International Study of Cancers of the Urothelium (RISC) who received fPBC for mUC and at least two cycles of subsequent chemotherapy were included in this study. A multivariable Cox proportional hazards model compared overall survival (OS) and progression-free survival (PFS).
RESULTS
One hundred thirty-five patients received sPBC and 161 received sNPBC. Baseline characteristics were similar between groups, except patients who received sPBC had higher baseline hemoglobin, higher disease control rate with fPBC, and longer time since fPBC. OS was superior in the sPBC group (median 7.9 vs 5.5 months) in a model adjusting for comorbidity burden, performance status, liver metastases, number of fPBC cycles received, best response to fPBC, and time since fPBC (hazard ratio, 0.72; 95% confidence interval, 0.53-0.98; p = .035). There was no difference in PFS. More patients in the sPBC group achieved disease control than in the sNPBC group (57.4% vs 44.8%; p = .041). Factors associated with achieving disease control in the sPBC group but not the sNPBC group included longer time since fPBC, achieving disease control with fPBC, and absence of liver metastases.
CONCLUSION
After receiving fPBC for mUC, patients who received sPBC had better OS and disease control. This may help inform the choice of subsequent chemotherapy in patients with mUC.
IMPLICATIONS FOR PRACTICE
Patients with progressive metastatic urothelial carcinoma after first-line platinum-based combination chemotherapy may now receive immuno-oncology agents, erdafitinib, enfortumab vedotin, or sacituzumab govitecan-hziy; however, those ineligible for these later-line therapies or who progress after receiving them may be considered for subsequent chemotherapy. In this retrospective study of 296 patients, survival outcomes and disease control rates were better in those receiving subsequent platinum-based rechallenge compared with non-platinum-based chemotherapy, suggesting that patients should receive platinum rechallenge if clinically able. Disease control with platinum rechallenge was more likely with prior first-line platinum having achieved disease control, longer time since first-line platinum, and absence of liver metastases.

Identifiants

pubmed: 34355457
doi: 10.1002/onco.13925
pmc: PMC8649023
doi:

Substances chimiques

Platinum 49DFR088MY

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1026-1034

Informations de copyright

© 2021 AlphaMed Press.

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Auteurs

Risa L Wong (RL)

Department of Medicine, University of Washington, Seattle, Washington, USA.
Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.

Lorin A Ferris (LA)

Department of Medicine, University of Washington, Seattle, Washington, USA.

Olivia A Do (OA)

Department of Medicine, University of Washington, Seattle, Washington, USA.

Sarah K Holt (SK)

Department of Urology, University of Washington, Seattle, Washington, USA.

Jorge D Ramos (JD)

Department of Medicine, University of Washington, Seattle, Washington, USA.
Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.

Simon J Crabb (SJ)

Cancer Sciences Unit, University of Southampton, Southampton, United Kingdom.

Cora N Sternberg (CN)

Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, New York, USA.

Joaquim Bellmunt (J)

Hospital Del Mar, Barcelona, Spain.

Sylvain Ladoire (S)

Georges-François Leclerc Cancer Center, Dijon, France.

Ugo De Giorgi (U)

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori IRCCS, Meldola, Italy.

Lauren C Harshman (LC)

Dana-Farber Cancer Institute, Boston, Massachusetts, USA.

Ulka N Vaishampayan (UN)

Karmanos Cancer Institute, Wayne State University, Detroit, Michigan, USA.

Andrea Necchi (A)

Fondazione IRCCS Instituto Nazionale dei Tumori, Milan, Italy.

Sandy Srinivas (S)

Stanford University, Palo Alto, California, USA.

Sumanta K Pal (SK)

City of Hope Comprehensive Cancer Center, Duarte, California, USA.

Guenter Niegisch (G)

Department of Urology, Medical Faculty, Heinrich-Heine-University, Germany.

Tanya B Dorff (TB)

University of Southern California Norris Comprehensive Cancer Center, Los Angeles, California, USA.

Matthew D Galsky (MD)

Mount Sinai Medical Center, New York, New York, USA.

Evan Y Yu (EY)

Department of Medicine, University of Washington, Seattle, Washington, USA.
Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.

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