TY - JOUR
T1 - Sentinel Lymph Node Biopsy Is Prognostic in Thickest Melanoma Cases and Should Be Performed for Thick Melanomas
AU - Han, Dale
AU - Han, Gang
AU - Duque, Monica T.
AU - Morrison, Steven
AU - Leong, Stanley P.
AU - Kashani-Sabet, Mohammed
AU - Vetto, John
AU - White, Richard
AU - Schneebaum, Schlomo
AU - Pockaj, Barbara
AU - Mozzillo, Nicola
AU - Sondak, Vernon K.
AU - Zager, Jonathan S.
N1 - Publisher Copyright:
© 2020, Society of Surgical Oncology.
PY - 2021/2
Y1 - 2021/2
N2 - Background: Sentinel lymph node biopsy (SLNB) is recommended for intermediate thickness melanoma, but for thick melanoma, guidelines are less definitive about the use of SLNB in this population. We present a study on thick melanoma evaluating for prognostic factors. Patients and Methods: The Sentinel Lymph Node Working Group database was queried for thick (> 4 mm) melanoma cases that had a SLNB from 1993 to 2018. Clinicopathologic characteristics were correlated with SLN status and melanoma-specific survival (MSS). Results: There were 1235 patients. Median follow-up was 28 months. Median thickness was 5.9 mm, with 956, 175, and 104 cases presenting thickness > 4–8, > 8–12, and > 12 mm, respectively. SLN metastases were seen in 439 of 1235 (35.5%) cases and in 33.9%, 40.6%, and 42.3% of melanomas > 4–8, > 8–12, and > 12 mm, respectively. In each thickness group, MSS was significantly worse for SLN-positive compared with SLN-negative cases (all P < 0.005). Multivariable analysis showed that SLN metastasis, male gender, increasing thickness, lymphovascular invasion, and microsatellitosis significantly predicted worse MSS for melanomas > 4–8 mm, with SLN metastasis showing the greatest risk (HR 2.17, 95% CI 1.64–2.87, P < 0.0001). For melanomas > 8 mm, only SLN metastasis significantly predicted MSS (> 8–12 mm: HR 3.93, 95% CI 2.00–7.73, P < 0.0001; > 12 mm: HR 3.58, 95% CI 1.56–8.22, p < 0.0027). Conclusions: Thick melanoma patients with SLN metastasis have significantly worse MSS compared with SLN-negative patients, even in the thickest cases, and SLN status is the most powerful and/or only predictor of MSS. Given these results, SLNB shows important prognostic value in this population and is indicated for clinically localized thick melanoma.
AB - Background: Sentinel lymph node biopsy (SLNB) is recommended for intermediate thickness melanoma, but for thick melanoma, guidelines are less definitive about the use of SLNB in this population. We present a study on thick melanoma evaluating for prognostic factors. Patients and Methods: The Sentinel Lymph Node Working Group database was queried for thick (> 4 mm) melanoma cases that had a SLNB from 1993 to 2018. Clinicopathologic characteristics were correlated with SLN status and melanoma-specific survival (MSS). Results: There were 1235 patients. Median follow-up was 28 months. Median thickness was 5.9 mm, with 956, 175, and 104 cases presenting thickness > 4–8, > 8–12, and > 12 mm, respectively. SLN metastases were seen in 439 of 1235 (35.5%) cases and in 33.9%, 40.6%, and 42.3% of melanomas > 4–8, > 8–12, and > 12 mm, respectively. In each thickness group, MSS was significantly worse for SLN-positive compared with SLN-negative cases (all P < 0.005). Multivariable analysis showed that SLN metastasis, male gender, increasing thickness, lymphovascular invasion, and microsatellitosis significantly predicted worse MSS for melanomas > 4–8 mm, with SLN metastasis showing the greatest risk (HR 2.17, 95% CI 1.64–2.87, P < 0.0001). For melanomas > 8 mm, only SLN metastasis significantly predicted MSS (> 8–12 mm: HR 3.93, 95% CI 2.00–7.73, P < 0.0001; > 12 mm: HR 3.58, 95% CI 1.56–8.22, p < 0.0027). Conclusions: Thick melanoma patients with SLN metastasis have significantly worse MSS compared with SLN-negative patients, even in the thickest cases, and SLN status is the most powerful and/or only predictor of MSS. Given these results, SLNB shows important prognostic value in this population and is indicated for clinically localized thick melanoma.
UR - http://www.scopus.com/inward/record.url?scp=85086324276&partnerID=8YFLogxK
U2 - 10.1245/s10434-020-08706-0
DO - 10.1245/s10434-020-08706-0
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C2 - 32524460
AN - SCOPUS:85086324276
SN - 1068-9265
VL - 28
SP - 1007
EP - 1016
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
IS - 2
ER -