Dermal melanoma: A report on prognosis, outcomes, and the utility of sentinel lymph node biopsy. Issue 1 (10th December 2015)

• Record Type: Journal Article
• Authors: Doepker, Matthew P.; Thompson, Zachary J.; Harb, Jennifer N.; Messina, Jane L.; Puleo, Christopher A.; Egan, Kathleen M.; Sarnaik, Amod A.; Gonzalez, Ricardo J.; Sondak, Vernon K.; Zager, Jonathan S.
• Is Part Of: Journal of surgical oncology. Volume 113:Issue 1(2016)
• Page Start: 98
• Page End: 102
• Publication Date: 2015-12-10
• Subjects: dermatopathologist -- in‐transit disease -- regression -- metastases; Cancer -- Surgery -- Periodicals; Neoplasms -- Periodicals; 616
• DOI: 10.1002/jso.24088
• Languages: English
• ISSNs: 0022-4790

Abstract

Abstract : Introduction: Historically dermal melanoma (DM) has been labeled as either stage IIIB (in‐transit) or stage IV (M1a) disease. We sought to investigate the natural history of DM and the utility and prognostic significance of sentinel lymph node biopsy (SLNB). Methods: Patients with DM undergoing SLNB at a single center from 1998 to 2009 were identified. Results: Eighty‐three patients met criteria, 10 (12%) patients had a positive SLNB. Of those, 5 (50%) recurred (all with distant disease). Twenty‐one (29%) of the 73 SLNB negative patients recurred and of those, 15 (71%) developed distant metastases, whereas 6 (29%) developed local or regional recurrence, including two false‐negative regional nodal recurrences. No in‐transit recurrences were recorded. Five‐year recurrence‐free and disease‐specific survival was significantly better for patients with a negative SLNB versus positive SLNB (56.8% vs. 22.2% P = 0.02, 81.1% vs. 61.0%, P = 0.05, respectively). Conclusion: SLNB has prognostic significance for RFS and DSS, and should be utilized in the management of DM based on a >10% yield and low false‐negative rate. Our data demonstrate patients with DM do not recur in an in‐transit fashion, which along with the survival outcomes suggest the behavior of DM is consistent with primary cutaneous melanoma of similar thickness rather than an isolated in‐transit or distant dermal metastasis from a regressed cutaneous primary. J. Surg. Oncol. 2016;113:98–102 . © 2015 Wiley Periodicals, Inc.