Enfortumab vedotin induced cutaneous manifestations

Enfortumab vedotin(EV) comprises of an anti–nectin-4 monoclonal antibody bound to the chemotherapeutic agent called monomethyl auristatin E, forming an antibody-drug conjugate. It is currently approved for the treatment of locally advanced or metastatic urothelial carcinoma after disease progression on two prior lines of therapy including chemotherapy and immunotherapy. Since nectin-4 is also expressed on the surface of keratinocytes, cutaneous adverse effects are common. Our clinical image depicts a cutaneous adverse reaction to EV and its resolution after discontinuation of EV.

Authors

Publication Details

Journal
Advances in Clinical Medical Research and Healthcare Delivery
Published
2025-02-04
DOI
https://doi.org/10.53785/2769-2779.1269
Primary Topic
Autoimmune Bullous Skin Diseases
Type
article
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article

Enfortumab vedotin induced cutaneous manifestations

Farhan Imran, Zeni Kharel
Advances in Clinical Medical Research and Healthcare Delivery
Autoimmune Bullous Skin Diseases
article

Enfortumab vedotin induced cutaneous manifestations

Farhan Imran, Zeni Kharel
article en

Abstract

Enfortumab vedotin(EV) comprises of an anti–nectin-4 monoclonal antibody bound to the chemotherapeutic agent called monomethyl auristatin E, forming an antibody-drug conjugate. It is currently approved for the treatment of locally advanced or metastatic urothelial carcinoma after disease progression on two prior lines of therapy including chemotherapy and immunotherapy. Since nectin-4 is also expressed on the surface of keratinocytes, cutaneous adverse effects are common. Our clinical image depicts a cutaneous adverse reaction to EV and its resolution after discontinuation of EV.

Advances in Clinical Medical Research and Healthcare DeliveryVol. 5(1)
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Openalex Percentile: Top 97%
Autoimmune Bullous Skin Diseases
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Enfortumab vedotin induced cutaneous manifestations — Farhan Imran, Zeni Kharel · Advances in Clinical Medical Research and Healthcare Delivery (2025) | TGRS Research Map | TGRS