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Immunotherapy in Basal Cell Carcinoma

Overview
Journal J Clin Med
Specialty General Medicine
Date 2024 Oct 16
PMID 39407789
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Abstract

Basal cell carcinoma (BCC) is the most frequent of all cancers, with an increasing incidence. The first line therapy is surgical excision, but topical therapies can be used in low-risk superficial BCCs, while the more advanced, unresectable, or metastatic BCCs benefit from systemic therapies with hedgehog inhibitors and immunotherapy. The purpose of this review is to highlight local and systemic immunotherapies and their efficacy in the management of BCCs. Local therapies can be considered in superficial and low-risk nodular BCCs, with imiquimod frequently used for its antitumor and immunoregulatory properties. Imiquimod alone demonstrated higher histological clearance rates, but patients treated with imiquimod experienced more adverse events than ones treated with other therapies. Imiquimod can be used as an adjuvant before Mohs micrographic surgery and can also be combined with other local therapies, like curettage, electrodesiccation, cryosurgery, and photodynamic therapy, with some treatment methods yielding results comparable with the surgery. Interferons and Interleukin-2 were evaluated in a small number of studies with different results. Systemic immunotherapies with programmed death-ligand 1 (PD-L1) inhibitors showed inconsistent results in patients with advanced BCCs, being effective in some patients that progressed on or were intolerant to hedgehog pathway inhibitors (HHI).

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References
1.
Sanchez V, Carpio E, Fardales V, Martinez B, Arias A, Brito E . Long-term follow-up of patients with high-risk facial basal cell carcinoma treated with interferon. An Bras Dermatol. 2024; 99(3):391-397. PMC: 11074603. DOI: 10.1016/j.abd.2023.08.009. View

2.
Potestio L, Scalvenzi M, Lallas A, Martora F, Guerriero L, Fornaro L . Efficacy and Safety of Cemiplimab for the Management of Non-Melanoma Skin Cancer: A Drug Safety Evaluation. Cancers (Basel). 2024; 16(9). PMC: 11083599. DOI: 10.3390/cancers16091732. View

3.
Habets J, Tank B, Vuzevski V, van Reede E, Stolz E, van Joost T . Characterization of the mononuclear infiltrate in basal cell carcinoma: a predominantly T cell-mediated immune response with minor participation of Leu-7+ (natural killer) cells and Leu-14+ (B) cells. J Invest Dermatol. 1988; 90(3):289-92. DOI: 10.1111/1523-1747.ep12456065. View

4.
Dessinioti C, Stratigos A . Immunotherapy and Its Timing in Advanced Basal Cell Carcinoma Treatment. Dermatol Pract Concept. 2023; 13(4). PMC: 10656142. DOI: 10.5826/dpc.1304a252. View

5.
Urosevic M, Dummer R, Conrad C, Beyeler M, Laine E, Burg G . Disease-independent skin recruitment and activation of plasmacytoid predendritic cells following imiquimod treatment. J Natl Cancer Inst. 2005; 97(15):1143-53. DOI: 10.1093/jnci/dji207. View