Cancer Medicine (Aug 2019)

Survival analysis and sentinel lymph node status in thin cutaneous melanoma: A multicenter observational study

  • Antonio Tejera‐Vaquerizo,
  • Simone Ribero,
  • Susana Puig,
  • Aram Boada,
  • Sabela Paradela,
  • David Moreno‐Ramírez,
  • Javier Cañueto,
  • Blanca deUnamuno,
  • Ana Brinca,
  • Miguel A. Descalzo‐Gallego,
  • Simona Osella‐Abate,
  • Paola Cassoni,
  • Cristina Carrera,
  • Sergi Vidal‐Sicart,
  • Antoni Bennássar,
  • Ramón Rull,
  • Llucìa Alos,
  • Celia Requena,
  • Isidro Bolumar,
  • Víctor Traves,
  • Ángel Pla,
  • A. Fernández‐Orland,
  • Ane Jaka,
  • María T. Fernández‐Figueres,
  • Josep M. Hilari,
  • Pol Giménez‐Xavier,
  • Ricardo Vieira,
  • Rafael Botella‐Estrada,
  • Concepción Román‐Curto,
  • Lara Ferrándiz,
  • Nicolás Iglesias‐Pena,
  • Carlos Ferrándiz,
  • Josep Malvehy,
  • Pietro Quaglino,
  • Eduardo Nagore,
  • on behalf of SENTIMEL group

DOI
https://doi.org/10.1002/cam4.2358
Journal volume & issue
Vol. 8, no. 9
pp. 4235 – 4244

Abstract

Read online

Abstract Mitotic rate is no longer considered a staging criterion for thin melanoma in the 8th edition of the American Joint Committee on Cancer Staging Manual. The aim of this observational study was to identify prognostic factors for thin melanoma and predictors and prognostic significance of sentinel lymph node (SLN) involvement in a large multicenter cohort of patients with melanoma from nine tertiary care hospitals. A total of 4249 consecutive patients with thin melanoma diagnosed from January 1, 1998 to December 31, 2016 were included. The main outcomes were disease‐free interval and melanoma‐specific survival for the overall population and predictors of SLN metastasis (n = 1083). Associations between survival and SLN status and different clinical and pathologic variables (sex, age, tumor location, mitosis, ulceration, regression, lymphovascular invasion, histologic subtype, Clark level, and Breslow thickness) were analyzed by Cox proportional hazards regression and logistic regression. SLN status was the most important prognostic factor for melanoma‐specific survival (hazard ratio, 13.8; 95% CI, 6.1‐31.2; P 2 mitoses/mm2 was the only factor associated with a positive SLN biopsy (odds ratio, 2.9; 95% CI, 1.22‐7; P = 0.01. SLN status is the most important prognostic factor in thin melanoma. A high mitotic rate is associated with metastatic SLN involvement. SLN biopsy should be discussed and recommended in patients with thin melanoma and a high mitotic rate.

Keywords