TY - JOUR
T1 - Factors predictive of the status of sentinel lymph nodes in melanoma patients from a large multicenter database
AU - White, Richard L.R.
AU - Ayers, Gregory D.
AU - Stell, Virginia H.
AU - Ding, Shouluan
AU - Gershenwald, Jeffrey E.
AU - Salo, Jonathan C.
AU - Pockaj, Barbara A.
AU - Essner, Richard
AU - Faries, Mark
AU - Charney, Kim James
AU - Avisar, Eli
AU - Hauschild, Axel
AU - Egberts, Friederike
AU - Averbook, Bruce J.
AU - Garberoglio, Carlos A.
AU - Vetto, John T.
AU - Ross, Merrick I.
AU - Chu, David
AU - Trisal, Vijay
AU - Hoekstra, Harald
AU - Whitman, Eric
AU - Wanebo, Harold J.
AU - Debonis, Daniel
AU - Vezeridis, Michael
AU - Chevinsky, Aaron
AU - Kashani-Sabet, Mohammed
AU - Shyr, Yu
AU - Berry, Lynne
AU - Zhao, Zhiguo
AU - Soong, Seng Jaw
AU - Leong, Stanley P.L.
N1 - Funding Information:
ACKNOWLEDGMENT This study is supported in part by an educational grant from Schering Oncology. The authors thank Cissy Swartz for her editorial and logistic assistance.
PY - 2011/12
Y1 - 2011/12
N2 - Background: Numerous predictive factors for cutaneous melanoma metastases to sentinel lymph nodes have been identified; however, few have been found to be reproducibly significant. This study investigated the significance of factors for predicting regional nodal disease in cutaneous melanoma using a large multicenter database. Methods: Seventeen institutions submitted retrospective and prospective data on 3463 patients undergoing sentinel lymph node (SLN) biopsy for primary melanoma. Multiple demographic and tumor factors were analyzed for correlation with a positive SLN. Univariate and multivariate statistical analyses were performed. Results: Of 3445 analyzable patients, 561 (16.3%) had a positive SLN biopsy. In multivariate analysis of 1526 patients with complete records for 10 variables, increasing Breslow thickness, lymphovascular invasion, ulceration, younger age, the absence of regression, and tumor location on the trunk were statistically significant predictors of a positive SLN. Conclusions: These results confirm the predictive significance of the well-established variables of Breslow thickness, ulceration, age, and location, as well as consistently reported but less well-established variables such as lymphovascular invasion. In addition, the presence of regression was associated with a lower likelihood of a positive SLN. Consideration of multiple tumor parameters should influence the decision for SLN biopsy and the estimation of nodal metastatic disease risk.
AB - Background: Numerous predictive factors for cutaneous melanoma metastases to sentinel lymph nodes have been identified; however, few have been found to be reproducibly significant. This study investigated the significance of factors for predicting regional nodal disease in cutaneous melanoma using a large multicenter database. Methods: Seventeen institutions submitted retrospective and prospective data on 3463 patients undergoing sentinel lymph node (SLN) biopsy for primary melanoma. Multiple demographic and tumor factors were analyzed for correlation with a positive SLN. Univariate and multivariate statistical analyses were performed. Results: Of 3445 analyzable patients, 561 (16.3%) had a positive SLN biopsy. In multivariate analysis of 1526 patients with complete records for 10 variables, increasing Breslow thickness, lymphovascular invasion, ulceration, younger age, the absence of regression, and tumor location on the trunk were statistically significant predictors of a positive SLN. Conclusions: These results confirm the predictive significance of the well-established variables of Breslow thickness, ulceration, age, and location, as well as consistently reported but less well-established variables such as lymphovascular invasion. In addition, the presence of regression was associated with a lower likelihood of a positive SLN. Consideration of multiple tumor parameters should influence the decision for SLN biopsy and the estimation of nodal metastatic disease risk.
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U2 - 10.1245/s10434-011-1826-9
DO - 10.1245/s10434-011-1826-9
M3 - Article
C2 - 21647761
AN - SCOPUS:82955237235
SN - 1068-9265
VL - 18
SP - 3593
EP - 3600
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
IS - 13
ER -