New and topics: enfortumab vedotin mechanisms of response and resistance in urothelial cancer - What do we understand so far?

Publication/Presentation Date

10-1-2021

Abstract

Enfortumab vedotin (EV) was FDA approved in December 2019 for platinum- and checkpoint-refractory urothelial cancer based on an exceptional 44% response rate, and is currently approved for use after platinum and checkpoint inhibitor therapy. Enfortumab is an antibody-drug conjugate that targets Nectin-4, which is widely expressed in urothelial cancer. Despite this ample target, clinical benefit is not achieved by all patients, and mechanisms of treatment resistance are undescribed. Herein we summarize what is known to date regarding coorelative findings and subgroup analysis and EV response, including novel biopsy data in patients with tumor progression post EV.

Volume

39

Issue

10

First Page

619

Last Page

622

ISSN

1873-2496

Disciplines

Business Administration, Management, and Operations | Health and Medical Administration | Management Sciences and Quantitative Methods

PubMedID

34148797

Department(s)

Administration and Leadership

Document Type

Article

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