Journal of Clinical Oncology, Vol 17, Issue 3
(March), 1999: 976
© 1999 American Society for Clinical Oncology
Multi-Institutional Melanoma Lymphatic Mapping Experience: The Prognostic Value of Sentinel Lymph Node Status in 612 Stage I or II Melanoma Patients
Jeffrey E. Gershenwald,
William Thompson,
Paul F. Mansfield,
Jeffrey E. Lee,
Maria I. Colome,
Chi-hong Tseng,
J. Jack Lee,
Charles M. Balch,
Douglas S. Reintgen,
Merrick I. Ross
From the Departments of Surgical Oncology, Pathology, and Biomathematics, The University of Texas M.D. Anderson Cancer Center, Houston, TX; and the Cutaneous Oncology Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Address reprint requests to Merrick I. Ross, MD, Department of Surgical Oncology, The University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Blvd, Box 106, Houston, TX 77030.
PURPOSE: To compare the effect of pathologic sentinel lymph node (SLN) status with that of other known prognostic factors on recurrence and survival in patients with stage I or II cutaneous melanoma.
PATIENTS AND METHODS: We reviewed the records of 612 patients with primary cutaneous melanoma who underwent lymphatic mapping and SLN biopsy between January 1991 and May 1995 to determine the effects of tumor thickness, ulceration, Clark level, location, sex, and SLN pathologic status on disease-free and disease-specific survival.
RESULTS: In the 580 patients in whom lymphatic mapping and SLN biopsy were successful, the SLN was positive by conventional histology in 85 patients (15%) but negative in 495 patients (85%). SLN status was the most significant prognostic factor with respect to disease-free and disease-specific survival by univariate and multiple covariate analyses. Although tumor thickness and ulceration influenced survival in SLN-negative patients, they provided no additional prognostic information in SLN-positive patients.
CONCLUSION: Lymphatic mapping and SLN biopsy is highly accurate in staging nodal basins at risk for regional metastases in primary melanoma patients and identifies those who may benefit from earlier lymphadenectomy. Furthermore, pathologic status of the SLN in these patients with clinically negative nodes is the most important prognostic factor for recurrence. The information from SLN biopsy is particularly helpful in establishing stratification criteria for future adjuvant trials.
Presented at the 49th Annual Meeting of the Society of Surgical Oncology, Atlanta, GA, March 1996.

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B. Esmaeli, D. Reifler, V. G. Prieto, M. Amir Ahmadi, L. Hidaji, E. Delpassand, and M. I. Ross
Conjunctival Melanoma With a Positive Sentinel Lymph Node
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S. S. Dadras, T. Paul, J. Bertoncini, L. F. Brown, A. Muzikansky, D. G. Jackson, U. Ellwanger, C. Garbe, M. C. Mihm, and M. Detmar
Tumor Lymphangiogenesis: A Novel Prognostic Indicator for Cutaneous Melanoma Metastasis and Survival
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J. B. Lowe, E. Hurst, J. F. Moley, and L. A. Cornelius
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Arch Dermatol,
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[Abstract]
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R. J. Bleicher, R. Essner, L. J. Foshag, L. A. Wanek, and D. L. Morton
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R.J.C.L.M. Vuylsteke, P.A.M. van Leeuwen, M.G. S. Muller, H.A. Gietema, D.R. Kragt, and S. Meijer
Clinical Outcome of Stage I/II Melanoma Patients After Selective Sentinel Lymph Node Dissection: Long-Term Follow-Up Results
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V Davids, S H Kidson, and G S Hanekom
Accurate molecular detection of melanoma nodal metastases: an assessment of multimarker assay specificity, sensitivity, and detection rate
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K. M. McMasters, A. Sober, and J. M. Kirkwood
Sentinel Lymph Node Biopsy and Adjuvant Therapy for Melanoma: Evidence Revisited
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C. E. Schmalbach, B. Nussenbaum, R. S. Rees, J. Schwartz, T. M. Johnson, and C. R. Bradford
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I. A. Jacobs, C. K. Chang, T. K. DasGupta, and G. Salti
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D. Polsky, K. Melzer, C. Hazan, K. S. Panageas, K. Busam, M. Drobnjak, H. Kamino, J. G. Spira, A. W. Kopf, A. Houghton, et al.
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F. E. Schmidt, E. A. Woltering, W. R. Webb, O. M. Garcia, J. E. Cohen, and M. H. Rozans
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D Johnson and I H Whitworth
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T. Belhocine, G. Pierard, M. de Labrassinne, T. Lahaye, and P. Rigo
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K. M. McMasters, C. Chao, S. L. Wong, W. R. Wrightson, M. I. Ross, D. S. Reintgen, R. D. Noyes, P. B. Cerrito, M. J. Edwards, and for the Sunbelt Melanoma Trial Group
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K. L. Kilbridge, B. F. Cole, J. M. Kirkwood, F. G. Haluska, M. A. Atkins, J. C. Ruckdeschel, D. E. Sock, R. F. Nease Jr, and J. C. Weeks
Quality-of-Life-Adjusted Survival Analysis of High-Dose Adjuvant Interferon Alfa-2b for High-Risk Melanoma Patients Using Intergroup Clinical Trial Data
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S. A. Eicher, G. L. Clayman, J. N. Myers, and A. M. Gillenwater
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G. I. Salti, A. Kansagra, M. A. Warso, S. G. Ronan, and T. K. Das Gupta
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C. M. Balch and M. C. Mihm
Reply to the article "The AJCC staging proposal for cutaneous melanoma: comments by the EORTC Melanoma Group", by D. J. Ruiter et al. (Ann Oncol 2001; 12: 9-11)
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O. Alonso, M. Martinez, G. Lago, and J. Espasandin
Preoperative Evaluation of Sentinel Lymph Node Status in Melanoma by Means of 99mTc-MIBI and Lymphoscintigraphy: A Case Report
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P J Ell
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M. Kashani-Sabet, R. W. Sagebiel, C. M. M. Ferreira, M. Nosrati, and J. R. Miller III
Vascular Involvement in the Prognosis of Primary Cutaneous Melanoma
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R. W. Dubois, S. M. Swetter, M. Atkins, K. McMasters, R. Halbert, S. J. Miller, R. Shiell, and J. Kirkwood
Developing Indications for the Use of Sentinel Lymph Node Biopsy and Adjuvant High-Dose Interferon Alfa-2b in Melanoma
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J. Connors, B. Smoller, and S. Dinehart
Sentinel Node Biopsy for Melanoma: What Is the Evidence?
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C. M. Balch, S.-J. Soong, J. E. Gershenwald, J. F. Thompson, D. S. Reintgen, N. Cascinelli, M. Urist, K. M. McMasters, M. I. Ross, J. M. Kirkwood, et al.
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C. M. Balch, A. C. Buzaid, S.-J. Soong, M. B. Atkins, N. Cascinelli, D. G. Coit, I. D. Fleming, J. E. Gershenwald, A. Houghton Jr, J. M. Kirkwood, et al.
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K. M. McMasters, D. S. Reintgen, M. I. Ross, J. E. Gershenwald, M. J. Edwards, A. Sober, N. Fenske, F. Glass, C. M. Balch, and D. G. Coit
Sentinel Lymph Node Biopsy for Melanoma: Controversy Despite Widespread Agreement
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R Allan
Sentinel node localization: do or dye alone?
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K.M. Acland, C. Healy, E. Calonje, M. O'Doherty, T. Nunan, C. Page, E. Higgins, and R. Russell-Jones
Comparison of Positron Emission Tomography Scanning and Sentinel Node Biopsy in the Detection of Micrometastases of Primary Cutaneous Malignant Melanoma
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R. A. Valdés Olmos and O. E. Nieweg
Reproducibility of Cutaneous Lymphoscintigraphy: Same or Different Lymphatic Routes and Sentinel Nodes After Reinjection?
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B. Coldiron and S. P. L. Leong
No Evidence to Support Delay in Excision of Malignant Melanoma
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B. Cady
Sentinel Lymph Node Procedure in Squamous Cell Carcinoma of the Vulva
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J. A. de Hullu, H. Hollema, D. A. Piers, R. H. M. Verheijen, P. J. van Diest, M. J. E. Mourits, J. G. Aalders, and A. G. J. van der Zee
Sentinel Lymph Node Procedure Is Highly Accurate in Squamous Cell Carcinoma of the Vulva
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M. J. Liptay, G. A. Masters, D. J. Winchester, B. L. Edelman, B. J. Garrido, T. R. Hirschtritt, R. M. Perlman, and W. A. Fry
Intraoperative radioisotope sentinel lymph node mapping in non-small cell lung cancer
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J M. Thomas and E. J Patocskai
The argument against sentinel node biopsy for malignant melanoma
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J. D. Wagner, H.-M. Park, J. J. Coleman III, C. Love, and J. T. Hayes
Cervical Sentinel Lymph Node Biopsy for Melanomas of the Head and Neck and Upper Thorax
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R. M. MacKie
Melanoma and the Dermatologist in the Third Millennium
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S. P. L. Leong, T. A. Achtem, F. A. Habib, I. Steinmetz, E. Morita, R. E. Allen, M. Kashani-Sabet, and R. Sagebiel
Discordancy Between Clinical Predictions vs Lymphoscintigraphic and Intraoperative Mapping of Sentinel Lymph Node Drainage of Primary Melanoma
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