Successful treatment with avapritinib in patient with mucosal metastatic melanoma.

KIT inhibitor avapritinib mucosal melanoma targeted therapy vulvar melanoma

Journal

Therapeutic advances in medical oncology
ISSN: 1758-8340
Titre abrégé: Ther Adv Med Oncol
Pays: England
ID NLM: 101510808

Informations de publication

Date de publication:
2020
Historique:
received: 28 01 2020
accepted: 07 07 2020
entrez: 22 8 2020
pubmed: 22 8 2020
medline: 22 8 2020
Statut: epublish

Résumé

Metastatic vulvar melanoma is a rare and aggressive disease and survival is usually poor. Vulvar melanomas harbor BRAF V600 mutations only infrequently; consequently, target therapy is a rare therapeutic option and immunotherapy usually has only a weak effect. On the other hand, KIT mutations are rare in cutaneous melanomas, but relatively frequent in mucosal melanomas, particularly in vulvar-vaginal melanomas, and can be a therapeutic target. Herein, we report a clinical case of a patient with metastatic vulvar melanoma, harboring an exon 17 c-KIT mutation, treated with avapritinib (BLU-285) - a highly potent and selective oral kinase inhibitor designed to treat imatinib-resistant gastro-intestinal stromal tumors (GIST) by targeting KIT/PDGFRα activation loop mutants (exons 17/18). After failure of the combination of ipilimumab + nivolumab first and then nivolumab alone, the patient received avapritinib 300 mg/daily for central nervous system (CNS), lymph-nodal, right adrenal gland, lung, and subcutaneous metastases. Best response was partial remission, according to RECIST 1.1 criteria. Time to treatment progression was 11 months. Main toxicities were grade 2 cutaneous vasculitis that required avapritinib discontinuation, and grade 2 uveitis of unknown origin, treated by vitrectomy and empiric antibiotic and antiviral therapy due to negative cultural tests. Uveitis was detected at the time of progression and therapy was definitively discontinued. In conclusion, avapritinib proved to be effective even in the presence of a pretreated disease, a high tumor burden, and brain metastases. In our experience, treatment was feasible and toxicity manageable. Considering the lack of effective therapies and the poor outcome of the disease, determination of c-KIT mutations should be performed routinely in cases of metastatic mucosal melanoma.

Identifiants

pubmed: 32821296
doi: 10.1177/1758835920946158
pii: 10.1177_1758835920946158
pmc: PMC7406922
doi:

Types de publication

Case Reports

Langues

eng

Pagination

1758835920946158

Informations de copyright

© The Author(s), 2020.

Déclaration de conflit d'intérêts

Conflict of interest statement: Cocorocchio E.: paid consultant for Roche, Novartis, BMS Ferrucci PF: paid consultant for Roche, Novartis, BMS, Amgen, MSD.

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Auteurs

Emilia Cocorocchio (E)

Division of Medical Oncology of Melanoma, Soft Tissue Sarcoma and Rare Tumors, Istituto Europeo di Oncologia IRCCS, Via Giuseppe Ripamonti 435, Milano, 20141, Italy.

Laura Pala (L)

Division of Medical Oncology of Melanoma, Soft Tissue Sarcoma and Rare Tumors, Istituto Europeo di Oncologia IRCCS, Milan, Italy.

Fabio Conforti (F)

Division of Medical Oncology of Melanoma, Soft Tissue Sarcoma and Rare Tumors, Istituto Europeo di Oncologia IRCCS, Milan, Italy.

Elena Guerini-Rocco (E)

Pathology and Laboratory Medicine Department, Istituto Europeo di Oncologia IRCCS, Milan, Italy.

Tommaso De Pas (T)

Division of Medical Oncology of Melanoma, Soft Tissue Sarcoma and Rare Tumors, Istituto Europeo di Oncologia IRCCS, Milan, Italy.

Pier Francesco Ferrucci (PF)

Department of Experimental Oncology, Istituto Europeo di Oncologia IRCCS, Milan, Italy.

Classifications MeSH