Mohs Micrographic Surgery Using MART-1 Immunostain in the Treatment of Invasive Melanoma and Melanoma In Situ

Dermatol Surg. 2016 Jun;42(6):733-44. doi: 10.1097/DSS.0000000000000725.

Abstract

Background: Mohs micrographic surgery (MMS) with melanoma antigen recognized by T-cell (MART-1) immunostaining is an effective treatment of cutaneous melanoma.

Objective: To determine the efficacy of MMS with MART-1 immunostain in the management of invasive and in situ melanoma.

Methods and materials: A retrospective cohort study evaluated 2,114 melanomas in 1,982 patients excised using MMS and MART-1 immunostain. The margins required for excision were calculated based on Breslow thickness, location, and size. Survival and local recurrence rates were calculated and compared with those of historical controls.

Results: The mean follow-up period was 3.73 years. Local recurrence was identified in 0.49% (7/1,419) of primary melanomas. Approximately 82% of melanomas were excised with ≤6-mm margins. The surgical margin was significantly related to tumor location and size but not to Breslow thickness. The five-year Kaplan-Meier local recurrence and disease-specific survival rates were 0.59 ± 0.30 and 98.53 ± 0.42, respectively. Mohs micrographic surgery with MART-1 immunostain achieved lower local recurrence rates and equivalent or higher Kaplan-Meier survival rates than conventional wide local excision.

Conclusion: Mohs micrographic surgery with MART-1 immunostain is an effective treatment of melanoma as evidenced by low local recurrence rates. It offers the advantage of more tissue-conserving margins than those recommended for conventional excision.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Carcinoma in Situ / pathology
  • Carcinoma in Situ / surgery*
  • Child
  • Female
  • Humans
  • MART-1 Antigen / immunology*
  • Male
  • Melanoma / immunology
  • Melanoma / pathology
  • Melanoma / surgery*
  • Middle Aged
  • Mohs Surgery*
  • Neoplasm Invasiveness / pathology
  • Retrospective Studies
  • Skin Neoplasms / immunology
  • Skin Neoplasms / pathology
  • Skin Neoplasms / surgery*
  • Survival Rate
  • Treatment Outcome

Substances

  • MART-1 Antigen