Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 May 27;108(10):djw121.
doi: 10.1093/jnci/djw121. Print 2016 Oct.

De Novo vs Nevus-Associated Melanomas: Differences in Associations With Prognostic Indicators and Survival

Affiliations

De Novo vs Nevus-Associated Melanomas: Differences in Associations With Prognostic Indicators and Survival

Rachel M Cymerman et al. J Natl Cancer Inst. .

Abstract

Background: Although 20% to 30% of melanomas are histopathologically 'nevus associated,' the majority of melanomas arise de novo, ie, in clinically normal skin with no associated nevus. We examined whether these forms of melanoma differed in their associations with clinical and histopathologic features and patient survival.

Methods: We analyzed two prospective cohorts from our institution with protocol-driven follow-up information (NYU1, n = 1024; NYU2, n = 1125). We used univariate and multivariable analyses to examine associations between de novo vs nevus-associated melanoma classification and age, anatomic site, tumor thickness, tumor ulceration, mitotic index, histological subtype, clinical stage, and survival. We tested the associations identified in NYU1 using NYU2 as a replication cohort. All tests of statistical significance were two-sided.

Results: In NYU1, de novo melanomas were associated with tumor thickness greater than 1.0 mm (odds ratio [OR] = 1.96, 95% confidence interval [CI] = 1.43 to 2.70, P < .001), ulceration (OR = 1.65, 95% CI = 1.10 to 2.54, P = .02), nodular subtype (OR = 3.26, 95% CI = 1.70 to 7.11, P = .001), greater than stage I (OR = 2.35, 95% CI = 1.65 to 3.40, P < .001), older age (OR = 1.64, 95% CI = 1.18 to 2.30, P = .004), and shorter overall survival (HR = 1.63, 95% CI = 1.22 to 2.18, P < .001). In NYU2, de novo melanoma was again statistically significantly associated with thickness greater than 1.0 mm (OR = 2.24, 95% CI = 1.72 to 2.93, P < .001), ulceration (OR = 2.88, 95% CI = 1.95 to 4.37, P < .001), nodular subtype (OR = 2.41, 95% CI = 1.75 to 3.37, P < .001), greater than stage I (OR = 2.42, 95% CI = 1.80 to 3.29, P < .001), older age (OR = 1.68, 95% CI = 1.31 to 2.17, P < .001), and shorter overall survival (HR = 2.52, 95% CI = 1.78 to 3.56, P < .001). In multivariable analysis, de novo classification was an independent, poor prognostic indicator in NYU2 (HR = 1.70, 95% CI = 1.19 to 2.44, P = .004). Male patients had a statistically significantly worse survival than female patients if their melanoma was de novo (NYU1, P < .001; NYU2, P < .001); unexpectedly, there was no sex difference in survival among patients with nevus-associated tumors.

Conclusions: These data suggest that de novo melanomas are more aggressive than nevus-associated melanomas. This classification scheme may also provide a useful framework for investigations into sex differences in melanoma outcomes.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Overall survival stratified by de novo ( solid lines ) or nevus-associated ( dashed lines ) melanoma classification. A) NYU1 cohort. B) NYU2 cohort. Tables of the numbers of patients at risk at different time points are given below each graph. P values are calculated based on two-sided log-rank test.
Figure 2.
Figure 2.
Overall survival analyses for nevus-associated and de novo melanoma patients stratified by sex ( solid lines = male; dashed lines = female). A) NYU1 = nevus-associated patients. B) NYU1 = de novo patients. C) NYU2 = nevus-associated patients. D) NYU2 = de novo patients. Tables of the numbers of patients at risk at different time points are given below each graph. P values are calculated based on two-sided log-rank test.

References

    1. Goldstein AM, Tucker MA . Dysplastic nevi and melanoma . Cancer Epidemiol Biomarkers Prev . 2013. ; 22 ( 4 ): 528 - 532 . - PMC - PubMed
    1. Stolz W, Schmoeckel C, Landthaler M , et al. . Association of early malignant melanoma with nevocytic nevi . Cancer. 1989. ; 63 ( 3 ): 550 - 555 . - PubMed
    1. Black WC. Residual dysplastic and other nevi in superficial spreading melanoma. Clinical correlations and association with sun damage . Cancer. 1988. ; 62 ( 1 ): 163 - 173 . - PubMed
    1. Clark WH, Jr, Elder DE, Guerry Dt , et al. . A study of tumor progression: the precursor lesions of superficial spreading and nodular melanoma . Hum Pathol. 1984. ; 15 ( 12 ): 1147 - 1165 . - PubMed
    1. Cook MG, Robertson I. Melanocytic dysplasia and melanoma . Histopathology. 1985. ; 9 ( 6 ): 647 - 658 . - PubMed

Publication types

MeSH terms