Multidisciplinary Care for Melanoma of Unknown Primary: Experience in the Era of Molecular Profiling

Ann Surg Oncol. 2020 Dec;27(13):5240-5247. doi: 10.1245/s10434-020-09112-2. Epub 2020 Sep 9.

Abstract

Background: Melanoma of unknown primary (MUP) accounts for approximately 3% of melanoma diagnoses. This study sought to evaluate treatment and outcomes for a modern MUP cohort.

Methods: A retrospective review of MUP was performed at a tertiary referral cancer center.

Results: Of 815 melanoma patients, 67 (8.2%) had MUP. Men were more likely to have MUP than women (67% vs. 55%; p = 0.04). The most common sites of MUP were lymph nodes (28%), visceral solid organs (25%), brain (16%), and skin/subcutaneous tissues (10%). Of the patients who underwent tumor genomic profiling, 52% harbored pathogenic BRAF mutations. Of the 24 patients who underwent multi-gene panel testing, all had pathogenic mutations and 21 (88%) had mutations in addition to or exclusive of BRAF, including 11 patients (46%) with telomerase reverse transcriptase promoter mutations. Checkpoint inhibitors (39%) and BRAF-MEK inhibitors (7%) were the most common first-line treatments. Upfront surgical resection was used for 25% of the MUP patients, and 12 of these resections were for curative intent. During a median follow-up period of 22.1 months, the median overall survival (OS) was not met for the patients with MUP isolated to lymph nodes. At 56.8 months, 75% of these patients were alive. The median OS was 37.4 months for skin/soft tissue MUP, 33.3 months for single solid organ viscera MUP, and 29.8 months for metastatic brain MUP.

Conclusion: Multigene panel testing identified pathogenic mutations in all tested MUP patients and frequently identified targets outside BRAF. Despite advanced stage, aggressive multimodal therapy for MUP can be associated with 5-year OS and should be pursued for appropriate candidates.

MeSH terms

  • Female
  • Humans
  • Lymph Nodes
  • Male
  • Melanoma* / genetics
  • Melanoma* / therapy
  • Mutation
  • Neoplasms, Unknown Primary* / genetics
  • Neoplasms, Unknown Primary* / therapy
  • Proto-Oncogene Proteins B-raf / genetics
  • Retrospective Studies
  • Skin Neoplasms* / genetics
  • Skin Neoplasms* / therapy

Substances

  • Proto-Oncogene Proteins B-raf