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The interval between primary melanoma excision and sentinel node biopsy is not associated with survival in sentinel node positive patients - An EORTC Melanoma Group study.

Oude Ophuis, CMC; Verhoef, C; Rutkowski, P; Powell, BWEM; van der Hage, JA; van Leeuwen, PAM; Voit, CA; Testori, A; Robert, C; Hoekstra, HJ; et al. Oude Ophuis, CMC; Verhoef, C; Rutkowski, P; Powell, BWEM; van der Hage, JA; van Leeuwen, PAM; Voit, CA; Testori, A; Robert, C; Hoekstra, HJ; Grünhagen, DJ; Eggermont, AMM; van Akkooi, ACJ (2016) The interval between primary melanoma excision and sentinel node biopsy is not associated with survival in sentinel node positive patients - An EORTC Melanoma Group study. Eur J Surg Oncol, 42 (12). pp. 1906-1913. ISSN 1532-2157 https://doi.org/10.1016/j.ejso.2016.05.012
SGUL Authors: Powell, Barry

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Abstract

BACKGROUND: Worldwide, sentinel node biopsy (SNB) is the recommended staging procedure for stage I/II melanoma. Most melanoma guidelines recommend re-excision plus SNB as soon as possible after primary excision. To date, there is no evidence to support this timeframe. AIM: To determine melanoma specific survival (MSS) for time intervals between excisional biopsy and SNB in SNB positive patients. METHODS: Between 1993 and 2008, 1080 patients were diagnosed with a positive SNB in nine Melanoma Group centers. We selected 1015 patients (94%) with known excisional biopsy date. Time interval was calculated from primary excision until SNB. Kaplan-Meier estimated MSS was calculated for different cutoff values. Multivariable analysis was performed to correct for known prognostic factors. RESULTS: Median age was 51 years (Inter Quartile Range (IQR) 40-62 years), 535 (53%) were men, 603 (59%) primary tumors were located on extremities. Median Breslow thickness was 3.00 mm (IQR 1.90-4.80 mm), 442 (44%) were ulcerated. Median follow-up was 36 months (IQR 20-62 months). Median time interval was 47 days (IQR 32-63 days). Median Breslow thickness was equal for both <47 days and ≥47 days interval: 3.00 mm (1.90-5.00 mm) vs 3.00 mm (1.90-4.43 mm) (p = 0.402). Sentinel node tumor burden was significantly higher in patients operated ≥47 days (p = 0.005). Univariate survival was not significantly different for median time interval. Multivariable analysis confirmed that time interval was no independent prognostic factor for MSS. CONCLUSIONS: Time interval from primary melanoma excision until SNB was no prognostic factor for MSS in this SNB positive cohort. This information can be used to counsel patients.

Item Type: Article
Additional Information: © 2016. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
Keywords: Cutaneous melanoma, Melanoma, Melanoma specific survival, Prognosis, Sentinel lymph node biopsy, Waiting list, Adult, Cohort Studies, Female, Humans, Kaplan-Meier Estimate, Male, Melanoma, Middle Aged, Multivariate Analysis, Prognosis, Retrospective Studies, Sentinel Lymph Node, Sentinel Lymph Node Biopsy, Skin Neoplasms, Survival Rate, Time Factors, Tumor Burden, Waiting Lists, Humans, Melanoma, Skin Neoplasms, Sentinel Lymph Node Biopsy, Prognosis, Tumor Burden, Survival Rate, Multivariate Analysis, Retrospective Studies, Cohort Studies, Time Factors, Adult, Middle Aged, Waiting Lists, Female, Male, Kaplan-Meier Estimate, Sentinel Lymph Node, Cutaneous melanoma, Melanoma, Sentinel lymph node biopsy, Melanoma specific survival, Prognosis, Waiting list, Cutaneous melanoma, Melanoma, Melanoma specific survival, Prognosis, Sentinel lymph node biopsy, Waiting list, Adult, Cohort Studies, Female, Humans, Kaplan-Meier Estimate, Male, Melanoma, Middle Aged, Multivariate Analysis, Prognosis, Retrospective Studies, Sentinel Lymph Node, Sentinel Lymph Node Biopsy, Skin Neoplasms, Survival Rate, Time Factors, Tumor Burden, Waiting Lists, 1112 Oncology And Carcinogenesis, Oncology & Carcinogenesis
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Eur J Surg Oncol
ISSN: 1532-2157
Language: eng
Dates:
DateEvent
December 2016Published
27 May 2016Published Online
15 May 2016Accepted
Publisher License: Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0
PubMed ID: 27266406
Web of Science ID: WOS:000390503100019
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/110383
Publisher's version: https://doi.org/10.1016/j.ejso.2016.05.012

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