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Distinct Clinicopathological and Prognostic Features of Thin Nodular Primary Melanomas: An International Study from 17 Centers

  • C. Dessinioti
  • , N. Dimou
  • , A. C. Geller
  • , A. Stergiopoulou
  • , S. Lo
  • , U. Keim
  • , J. E. Gershenwald
  • , L. E. Haydu
  • , S. Ribero
  • , P. Quaglino
  • , S. Puig
  • , J. Malvehy
  • , L. Kandolf-Sekulovic
  • , T. Radevic
  • , R. Kaufmann
  • , L. Meister
  • , E. Nagore
  • , V. Traves
  • , G. G. Champsas
  • , M. Plaka
  • B. Dreno, E. Varey, D. M. Ramirez, R. Dummer, J. Mangana, A. Hauschild, F. Egberts, Ketty Peris, Regno L. Del, Forsea A. -M., S. A. Zurac, R. Vieira, A. Brinca, I. Zalaudek, T. Deinlein, E. Linos, E. Evangelou, J. F. Thompson, R. A. Scolyer, C. Garbe, A. J. Stratigos

Research output: Contribution to journalArticle

Abstract

BACKGROUND: Nodular melanoma (NM) is more likely to be fatal compared with other melanoma subtypes, an effect attributed to its greater Breslow thickness. METHODS: Clinicopathological features of NM and superficial spreading melanoma (SSM) diagnosed in 17 centers in Europe (n = 15), the United States, and Australia between 2006 and 2015, were analyzed by multivariable logistic regression analysis, with emphasis on thin (T1 ≤ 1.0 mm) melanomas. Cox analysis assessed melanoma-specific survival. All statistical tests were two sided. RESULTS: In all, 20 132 melanomas (NM: 5062, SSM: 15 070) were included. Compared with T1 SSM, T1 NM was less likely to have regression (odds ratio [OR] = 0.46, 95% confidence interval [CI] = 0.29 to 0.72) or nevus remnants histologically (OR = 0.60, 95% CI = 0.42 to 0.85), and more likely to have mitoses (OR = 1.97, 95% CI = 1.33 to 2.93) and regional metastasis (OR = 1.77, 95% CI = 1.02 to 3.05). T1 NM had a higher mitotic rate than T1 SSM (adjusted geometric mean = 2.2, 95% CI = 1.9 to 2.5 vs 1.6, 95% CI = 1.5 to 1.7 per mm2, P < .001). Cox multivariable analysis showed a higher risk for melanoma-specific death for NM compared with SSM for T1 (HR = 2.10, 95% CI = 1.24 to 3.56) and T2 melanomas (HR = 1.30, 95% CI = 1.01 to 1.68), and after accounting for center heterogeneity, the difference was statistically significant only for T1 (HR = 2.20, 95% CI = 1.28 to 3.78). The NM subtype did not confer increased risk within each stratum (among localized tumors or cases with regional metastasis). CONCLUSIONS: T1 NM (compared with T1 SSM) was associated with a constellation of aggressive characteristics that may confer a worse prognosis. Our results indicate NM is a high-risk melanoma subtype that should be considered for inclusion in future prognostic classifications of melanoma.
Original languageEnglish
Pages (from-to)1314-1322
Number of pages9
JournalJournal of the National Cancer Institute
Volume111
Issue number12
DOIs
Publication statusPublished - 2019

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

Keywords

  • nodular melanoma

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