| Literature DB >> 28960289 |
Aram Boada1, Antonio Tejera-Vaquerizo2, Simone Ribero3, Susana Puig4,5, David Moreno-Ramírez6, Miguel A Descalzo-Gallego7, María T Fierro3, Pietro Quaglino3, Cristina Carrera4,5, Josep Malvehy4,5, Sergi Vidal-Sicart8, Antoni Bennássar4, Ramón Rull9, Llucìa Alos10, Celia Requena11, Isidro Bolumar12, Víctor Traves13, Ángel Pla14, María T Fernández-Figueras15, Carlos Ferrándiz1, Iciar Pascual16, José L Manzano17, Marina Sánchez-Lucas18, Pol Giménez-Xavier4,5, Lara Ferrandiz6, Eduardo Nagore11.
Abstract
The clinical value of sentinel lymph node (SLN) biopsy in thick melanoma patients (Breslow >4 mm) has not been sufficiently studied. The aim of the study is to evaluate whether SLN biopsy increases survival in patients with thick cutaneous melanoma, and, as a secondary objective, to investigate correlations between survival and lymph node status. We included 1,211 consecutive patients with thick melanomas (>4 mm) registered in the participating hospitals' melanoma databases between 1997 and 2015. Median follow-up was 40 months. Of these patients, 752 were matched into pairs by propensity scores based on sex, age, tumor location, histologic features of melanoma, year of diagnosis, hospital and adjuvant interferon therapy. The SLN biopsy vs. observation was associated with better DFS [adjusted hazard ratio (AHR), 0.74; 95% confidence interval (CI) 0.61-0.90); p = 0.002] and OS (AHR, 0.75; 95% CI, 0.60-0.94; p = 0.013) but not MSS (AHR, 0.84; 95% CI, 0.65-1.08; p = 0.165). SLN-negative patients had better 5- and 10-year MSS compared with SLN-positive patients (65.4 vs. 51.9% and 48.3 vs. 38.8%; p = 0.01, respectively). As a conclusion, SLN biopsy was associated with better DFS but not MSS in thick melanoma patients after adjustment for classic prognostic factors. SLN biopsy is useful for stratifying these patients into different prognostic groups.Entities:
Keywords: melanoma; prognosis; propensity score; sentinel lymph node biopsy
Mesh:
Year: 2017 PMID: 28960289 DOI: 10.1002/ijc.31078
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396