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Annals of Surgical Oncology 9:137-141 (2002)
© 2002 Society of Surgical Oncology


ORIGINAL ARTICLES

Frequency of Nonsentinel Lymph Node Metastasis in Melanoma

Kelly M. McMasters, MD, PhD, Sandra L. Wong, MD, Michael J. Edwards, MD, Celia Chao, MD, Merrick I. Ross, MD, R. Dirk Noyes, MD, Vicki Viar, RN, MSN, Patricia B. Cerrito, PhD and Douglas S. Reintgen, MD for the Sunbelt Melanoma Trial Group

From the Division of Surgical Oncology, Department of Surgery (KMM, SLW, MJE, CC, VV), James Graham Brown Cancer Center and Department of Mathematics (PBC), University of Louisville, Louisville, Kentucky; the University of Texas M. D. Anderson Cancer Center (MIR), Houston, Texas; the LDS Hospital (RDN), Salt Lake City, Utah; and the University of South Florida (DSR), Moffitt Cancer Center, Tampa, Florida.

Correspondence: Address correspondence and reprint requests to: Kelly M. McMasters, MD, PhD, University of Louisville–Brown Cancer Center, 529 S. Jackson St., Louisville, KY 40202; Fax: 502-629-3393; E-mail: kelly.mcmasters{at}nortonhealthcare.org

Background: Completion lymph node dissection (CLND) may not be necessary for some patients because nodal metastasis is rarely detected beyond the sentinel lymph nodes (SLNs). This analysis was performed to determine, among patients with positive SLNs, the rate of nodal metastasis found in nonsentinel nodes (NSNs).

Methods: This analysis includes patients with positive sentinel nodes, detected by hematoxylin and eosin (H&E) staining or immunohistochemistry (IHC), who then underwent CLND.

Results: This analysis included 274 patients with at least one positive SLN who underwent CLND of 282 involved regional nodal basins. Of the 282 SLN-positive nodal basins, 45 (16%) were found to have positive NSNs in the CLND specimen. Breslow thickness, Clark level, presence of ulceration, histological subtype, presence of vertical growth phase, evidence of regression, presence of lymphovascular invasion, number of positive SLNs, age, sex, and presence of multiple draining nodal basins were not predictive of positive nodes in the CLND specimen. Patients with SLN metastases detected only by IHC had an equal likelihood of having positive NSNs as those patients with positive SLNs on H&E examination.

Conclusions: No patient population could be identified with minimal risk of non-SLN metastasis. When a positive SLN is identified on either H&E staining or IHC, CLND should be performed routinely.

Key Words: Melanoma • Sentinel lymph node • Lymph node dissection • Lymphatic mapping • Nonsentinel node




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