Mucosal melanoma arising in an advanced, unresectable, or metastatic setting presents distinct molecular features from cutaneous melanoma. When a KIT mutation is identified, it defines a specific, actionable subgroup that warrants a tailored treatment approach.
This protocol applies to patients with advanced, unresectable, or metastatic mucosal melanoma in whom molecular testing has confirmed a KIT mutation. Mucosal melanoma exhibits a higher KIT mutation rate than cutaneous melanoma, making routine molecular profiling essential to identify this targetable alteration.
DOI: 10.1200/EDBK-25-473858
MM exhibits a higher KIT mutation rate than CM, which may contribute to its greater responsiveness to KIT inhibitors than acral or sun-damaged melanomas.
the distinct genomic landscape of mucosal melanoma (MM; eg, KIT and NRAS mutations) underlines the need for routine molecular testing to identify actionable targets and tailor therapies, such as KIT inhibitors for KIT-mutant tumors or MEK inhibitors for NRAS-mutant cases.
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