Enfortumab Vedotin-related Cutaneous Toxicity and Radiographic Response in Patients with Urothelial Cancer: A Single-center Experience and Review of the Literature.

Advanced urothelial cancer African American Bladder cancer Cutaneous adverse events Disease response Enfortumab vedotin Metastatic urothelial cancer Skin toxicity Upper tract urothelial cancer Urothelial cancer

Journal

European urology open science
ISSN: 2666-1683
Titre abrégé: Eur Urol Open Sci
Pays: Netherlands
ID NLM: 101771568

Informations de publication

Date de publication:
Mar 2023
Historique:
accepted: 10 01 2023
entrez: 23 2 2023
pubmed: 24 2 2023
medline: 24 2 2023
Statut: epublish

Résumé

Enfortumab vedotin (EV) is an antibody-drug conjugate approved for the treatment of refractory advanced urothelial cancer. Cutaneous toxicity is well described but has not been correlated with response. In this retrospective single-center study, data from patients treated with more than one dose of EV between December 2017 and June 2022 were analyzed. Of 56 patients with a median age of 69 yr, 41 (73.2%) were male and 27 (48.2%) had any-grade skin toxicity. For all 51 patients evaluable by physician-assessed Response Evaluation Criteria in Solid Tumors (RECIST) criteria, the response rate was 41.2%. For those with cutaneous toxicity, the response rate was 57.7%; for those without cutaneous toxicity, it was 24.0% ( We evaluated patients with urothelial cancer who were treated at our institution with enfortumab vedotin (EV). We found that patients who experienced the common side effect of any type of skin toxicity, such as rash or itching, were more likely to have improvement in their cancer from EV treatment than those who did not experience skin toxicity. Patients with higher weight and body mass index when starting EV tended to have more skin toxicity. We conclude that presence of skin toxicity might help doctors make decisions about how to manage the care of patients with EV in the future.

Identifiants

pubmed: 36820243
doi: 10.1016/j.euros.2023.01.002
pii: S2666-1683(23)00002-2
pmc: PMC9937876
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100-103

Informations de copyright

© 2023 The Authors.

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Auteurs

Evangelia Vlachou (E)

The Johns Hopkins Greenberg Bladder Cancer Institute, Baltimore, MD, USA.

Andres Matoso (A)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Urology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

David McConkey (D)

The Johns Hopkins Greenberg Bladder Cancer Institute, Baltimore, MD, USA.

Yuezhou Jing (Y)

The James Buchanan Brady Urological Institute, Johns Hopkins University, Baltimore, MD, USA.

Burles Avner Johnson (BA)

The Johns Hopkins Greenberg Bladder Cancer Institute, Baltimore, MD, USA.
Johns Hopkins University Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.

Noah M Hahn (NM)

The Johns Hopkins Greenberg Bladder Cancer Institute, Baltimore, MD, USA.
The James Buchanan Brady Urological Institute, Johns Hopkins University, Baltimore, MD, USA.
Johns Hopkins University Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.

Jean Hoffman-Censits (J)

The Johns Hopkins Greenberg Bladder Cancer Institute, Baltimore, MD, USA.
The James Buchanan Brady Urological Institute, Johns Hopkins University, Baltimore, MD, USA.
Johns Hopkins University Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.

Classifications MeSH