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Clinical benefit with tebentafusp in a patient with GNAQ mutant metastatic blue nevus-associated melanoma

  • Matthew R. Kudelka
  • , Allison L. Richards
  • , Philip Friedlander
  • , Jedd D. Wolchok
  • , Andrea P. Moy
  • , Alexander N. Shoushtari

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Melanoma arising in association with a blue nevus (BN) is rare but has molecular similarities to uveal melanoma (UM), including GNAQ/11 mutations. Tebentafusp was recently approved for UM based on improved overall survival in a phase 3 study. We hypothesized that tebentafusp may be active in BN-associated melanoma. Here, we present a case of metastatic BN-associated melanoma with rapid response and ∼1 year of disease control on tebentafusp. We also explore molecular and histological features of secondary resistance. Our case highlights that PD-1-resistant melanomas should be screened for GNAQ/11 mutations, as tebentafusp may be a treatment option in this extremely rare disease.

Original languageEnglish
Article numbere009609
JournalJournal for ImmunoTherapy of Cancer
Volume12
Issue number11
DOIs
StatePublished - 17 Nov 2024

Keywords

  • Bispecific T cell engager - BiTE
  • Immunotherapy
  • Melanoma

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