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Treatment-related skin reactions in enfortumab vedotin as a surrogate marker of survival and treatment response.

Authors :
Nagayama, Jun
Inoue, Satoshi
Sai, Hiroki
Hayakawa, Akira
Yuguchi, Yuri
Suzuki, Tomohide
Matsui, Hirotaka
Yuba, Takuma
Morishita, Koya
Akamatsu, Shusuke
Source :
International Journal of Clinical Oncology. Feb2025, Vol. 30 Issue 2, p267-276. 10p.
Publication Year :
2025

Abstract

Background: Treatment-related skin reactions (TRSRs) induced by enfortumab vedotin (EV) targeting nectin-4 are among the most common adverse events. However, their association with survival and treatment response is poorly understood. Methods: We retrospectively identified patients who received EV from December 2021 to April 2023 at Nagoya University Hospital and its affiliated facilities and extracted clinical data from their medical records. We evaluated cancer-specific survival (CSS) and progression-free survival (PFS) as survival outcomes and overall response rate (ORR) and disease control rate (DCR) as treatment responses between patients with and without TRSRs. Results: In total, 67 eligible patients were identified. Thirty-four patients experienced TRSRs, and the remaining 33 did not experience TRSRs. The median follow-up period was 8 months. Patients in the TRSRs group demonstrated significantly longer median CSS (15 vs. 8 months; p = 0.003) and median PFS (10 vs. 5 months; p < 0.001) than the non-TRSRs. Regarding treatment response, the patients in the TRSRs group showed a favorable, albeit nonsignificant, treatment response trend compared with those in the non-TRSRs group (ORR, 73.5% vs. 51.5%; p = 0.107; DCR, 91.2 % vs. 81.8%; p = 0.444). Conclusions: Patients with TRSRs demonstrated more prolonged survival and superior treatment responses to EV treatment. The role of TRSR as a surrogate marker of EV's efficacy should be further explored in prospective and sufficiently powered studies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13419625
Volume :
30
Issue :
2
Database :
Academic Search Index
Journal :
International Journal of Clinical Oncology
Publication Type :
Academic Journal
Accession number :
182613331
Full Text :
https://doi.org/10.1007/s10147-024-02672-3