TY - JOUR
T1 - Prognostic Value of Nevus-Associated Melanoma in Patients with Melanoma
AU - Riaz, Nazia
AU - Huibers, Anne
AU - Leong, Stanley P.
AU - Kashani-Sabet, Mohammed
AU - White, Richard L.
AU - Vetto, John T.
AU - Schneebaum, Schlomo
AU - O’Donoghue, Cristina
AU - Howard, Harrison
AU - Avisar, Eli
AU - Namm, Jukes P.
AU - Kosiorek, Heidi
AU - Pockaj, Barbara
AU - Faries, Mark
AU - Karakousis, Giorgos
AU - Zager, Jonathan S.
AU - Olofsson Bagge, Roger
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025
Y1 - 2025
N2 - Background: Although most melanomas develop de novo, about 30% are nevus-associated melanomas, where the prognostic value is unclear. Our study aimed to determine whether nevus-associated melanoma is associated with sentinel lymph node (SLN) status and prognosis in patients with melanoma. Methods: The Sentinel Lymph Node Working Group database, which includes comprehensive clinicopathological and outcome data, was utilized to investigate the association of nevus-associated melanoma with SLN status as well as relapse-free (RFS), melanoma-specific (MSS), and overall survival (OS) using multivariable logistic regression and Cox regression modeling. Results: A total of 3447 adult patients with a median follow-up of 2.6 years (interquartile range 0.9–6.9) were evaluable. Compared with de novo melanomas, nevus-associated melanomas showed a significant correlation with younger age as well as favorable histological features. The presence of a nevus-associated melanoma was not identified as an independent factor for SLN status (odds ratio 1.06, 95% confidence interval [CI] 0.80–1.41; p = 0.68). Compared with de novo melanomas, nevus-associated melanomas provided independent prognostic information for a favorable RFS (hazard ratio [HR] 0.67, 95% CI 0.53–0.84; p < 0.001), MSS (HR 0.54, 95% CI 0.34–0.85; p = 0.008), and OS (HR 0.42, 95% CI 0.30–0.57; p < 0.001). Conclusion: Melanomas associated with pre-existing nevi appear to be an independent favorable prognostic factor for recurrence and survival and may potentially be used as a clinical parameter for identifying patients with lower risk of recurrence.
AB - Background: Although most melanomas develop de novo, about 30% are nevus-associated melanomas, where the prognostic value is unclear. Our study aimed to determine whether nevus-associated melanoma is associated with sentinel lymph node (SLN) status and prognosis in patients with melanoma. Methods: The Sentinel Lymph Node Working Group database, which includes comprehensive clinicopathological and outcome data, was utilized to investigate the association of nevus-associated melanoma with SLN status as well as relapse-free (RFS), melanoma-specific (MSS), and overall survival (OS) using multivariable logistic regression and Cox regression modeling. Results: A total of 3447 adult patients with a median follow-up of 2.6 years (interquartile range 0.9–6.9) were evaluable. Compared with de novo melanomas, nevus-associated melanomas showed a significant correlation with younger age as well as favorable histological features. The presence of a nevus-associated melanoma was not identified as an independent factor for SLN status (odds ratio 1.06, 95% confidence interval [CI] 0.80–1.41; p = 0.68). Compared with de novo melanomas, nevus-associated melanomas provided independent prognostic information for a favorable RFS (hazard ratio [HR] 0.67, 95% CI 0.53–0.84; p < 0.001), MSS (HR 0.54, 95% CI 0.34–0.85; p = 0.008), and OS (HR 0.42, 95% CI 0.30–0.57; p < 0.001). Conclusion: Melanomas associated with pre-existing nevi appear to be an independent favorable prognostic factor for recurrence and survival and may potentially be used as a clinical parameter for identifying patients with lower risk of recurrence.
KW - Cutaneous melanoma
KW - Preexisting nevi
KW - Prognosis
KW - Recurrent melanoma
KW - Sentinel lymph node
UR - http://www.scopus.com/inward/record.url?scp=85217401987&partnerID=8YFLogxK
U2 - 10.1245/s10434-025-16945-2
DO - 10.1245/s10434-025-16945-2
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C2 - 39893342
AN - SCOPUS:85217401987
SN - 1068-9265
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
ER -