Survival outcomes and interval between lymphoscintigraphy and SLNB in cutaneous melanoma- findings of a large prospective cohort study

被引:8
作者
O'Leary, Fionnuala M. [1 ]
Beadsmoore, Clare J. [2 ]
Pawaroo, Davina [2 ]
Skrypniuk, John [2 ]
Heaton, Martin J. [1 ]
Moncrieff, Marc D. [1 ,3 ]
机构
[1] Norfolk & Norwich Univ Hosp NHS Fdn Trust, Dept Plast & Reconstruct Surg, Colney Lane, Norwich NR4 7UY, Norfolk, England
[2] Norfolk & Norwich Univ Hosp NHS Fdn Trust, Dept Nucl Med, Colney Lane, Norwich NR4 7UY, Norfolk, England
[3] Univ East Anglia, Norwich Med Sch, Norwich Res Pk, Norwich NR9 7TJ, Norfolk, England
来源
EJSO | 2018年 / 44卷 / 11期
关键词
Melanoma; Sentinel node biopsy; Timing lymphoscintigraphy; SENTINEL LYMPH-NODE; INTRAOPERATIVE GAMMA-PROBE; SQUAMOUS-CELL CARCINOMA; BREAST-CANCER; MALIGNANT-MELANOMA; PROGNOSTIC-FACTORS; BLUE-DYE; BIOPSY; IDENTIFICATION; LOCALIZATION;
D O I
10.1016/j.ejso.2018.06.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Sentinel lymph node biopsy (SLNB) in cutaneous melanoma (CM) is performed to identify patient at risk of regional and distant relapse. We hypothesized that timing of lymphoscintigraphy may influence the accuracy of SLNB and patient outcomes. Methods: We reviewed prospective data on patients undergoing SLNB for CM at a large university cancer-center between 2008 and 2015, examining patient and tumor demographics and time between lymphoscintigraphy (LS) and SLNB. Kaplan-Meier survival analysis assessed disease-specific (DSS) and overall-survival (OS), stratified by timing of IS. Cox multivariate regression analysis assessed independent risk factors for survival. Results: We identified 1015 patients. Median follow-up was 45 months (IQR 26-68 months). Univariate analysis showed a 6.8% absolute DSS (HR 1.6 [1.03-2.48], p = 0.04) benefit and a 10.7% absolute OS (HR 1.64 [1.13-2.38], p = 0.01) benefit for patients whose SLNB was performed < 12 h of LS (n = 363) compared to those performed >12 h (n = 652). Multivariate analysis identified timing of LS as an independent predictor of OS (p = 0.007) and DSS (p = 0.016) when competing with age, sex, Breslow thickness (BT) and SLN status. No difference in nodal relapse rates (5.2% v 4.6%; p = 0.67) was seen. Both groups were matched for age, sex, BT and SLN status. Conclusion: These data have significant implications for SLNB services, suggesting delaying SLNB >12 h after LS using a Tc99-labelled nanocolloid has a significant negative survival impact for patients and should be avoided. We hypothesise that temporal tracer migration is the underlying cause and advocate further trials investigating alternative, 'stable' tracer-agents. (C) 2018 Elsevier Ltd, BASO similar to The Association for Cancer Surgery, and the European Society of Surgical Oncology. All rights reserved.
引用
收藏
页码:1768 / 1772
页数:5
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