Topical Immunotherapy for Actinic Keratosis and Field Cancerization.

5-fluorouracil actinic keratosis anti PDL-1 cancerization field diclofenac disodium imiquimod immunosuppression immunotherapy nicotinamide photodynamic therapy solid organ transplant vitamin D

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
12 Mar 2024
Historique:
received: 09 02 2024
revised: 03 03 2024
accepted: 08 03 2024
medline: 28 3 2024
pubmed: 28 3 2024
entrez: 28 3 2024
Statut: epublish

Résumé

This comprehensive review delves into various immunotherapeutic approaches for the management of actinic keratoses (AKs), precancerous skin lesions associated with UV exposure. Although there are treatments whose main mechanism of action is immune modulation, such as imiquimod or diclofenac, other treatments, apart from their main effect on dysplastic cells, exert some immunological action, which in the end contributes to their efficacy. While treatments like 5-fluorouracil, imiquimod, photodynamic therapy, and nicotinamide are promising in the management of AKs, especially in immunocompetent individuals, their efficacy is somewhat reduced in solid organ transplant recipients due to immunosuppression. The analysis extends to optimal combination, focusing on cryoimmunotherapy as the most relevant. New immunotherapies include resimiquimod, ingenol disoxate, N-phosphonacetyl-L-aspartate (PALA), or anti-PD1 that have shown promising results, although more studies are needed in order to standardize their use.

Identifiants

pubmed: 38539468
pii: cancers16061133
doi: 10.3390/cancers16061133
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Instituto de Salud Carlos III Ministerio de Ciencia e innovación, Feder Funds (FIS PI21/00953 and PI21/00315) and the Research Group of the Government of Aragon B59-23D Dermatología y Fotobiología.
ID : Instituto de Salud Carlos III Ministerio de Ciencia e innovación, Feder Funds (FIS PI21/00953 and PI21/00315) and the Research Group of the Government of Aragon B59-23D Dermatología y Fotobiología.

Auteurs

Laura Bernal Masferrer (L)

Service of Dermatology, Miguel Servet University Hospital, 50009 Zaragoza, Spain.

Tamara Gracia Cazaña (T)

Service of Dermatology, Miguel Servet University Hospital, 50009 Zaragoza, Spain.

Isabel Bernad Alonso (I)

Service of Dermatology, Miguel Servet University Hospital, 50009 Zaragoza, Spain.

Marcial Álvarez-Salafranca (M)

Service of Dermatology, Miguel Servet University Hospital, 50009 Zaragoza, Spain.

Manuel Almenara Blasco (M)

Service of Dermatology, Miguel Servet University Hospital, 50009 Zaragoza, Spain.

María Gallego Rentero (M)

Department of Biology, Universidad Autónoma de Madrid, 28049 Madrid, Spain.

Ángeles Juarranz de la Fuente (Á)

Department of Biology, Universidad Autónoma de Madrid, 28049 Madrid, Spain.

Yolanda Gilaberte (Y)

Service of Dermatology, Miguel Servet University Hospital, 50009 Zaragoza, Spain.

Classifications MeSH