Prognostic Usefulness of Sentinel Lymph Node Biopsy for Patients Who Have Clinically Node Negative, Localized, Primary Invasive Cutaneous Melanoma: A Bayesian Analysis Using Informative Published Reports

OBJECTIVE To assess the prognostic value of sentinel lymph node biopsy status for patients with localized, clinically node negative, primary invasive cutaneous melanoma. DESIGN Predictive value of positive or negative sentinel lymph node biopsy (SLNB) results for melanoma-related death, using raw nu...

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Veröffentlicht in:Archives of dermatology (1960) 2011-04, Vol.147 (4), p.408-415
1. Verfasser: Rhodes, Arthur R
Format: Artikel
Sprache:eng
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Zusammenfassung:OBJECTIVE To assess the prognostic value of sentinel lymph node biopsy status for patients with localized, clinically node negative, primary invasive cutaneous melanoma. DESIGN Predictive value of positive or negative sentinel lymph node biopsy (SLNB) results for melanoma-related death, using raw numbers from informative publications. SETTING AND PARTICIPANTS Reports comprising 50 patients with cutaneous melanoma who had undergone SLNB, based on PubMed search (January 1, 1993, through June 3, 2010). MAIN OUTCOME MEASURE Melanoma-related death. RESULTS For the 2 informative reports of patients with tumors of intermediate thickness (1-4 mm), risk of melanoma-related death ranged from 26.2% to 31.6% for node-positive cases and from 9.7% to 15.6% for node-negative cases. Based on 4 informative reports of patients with thin tumors (≤1 mm), risk of melanoma-related death ranged from 0% to 0.6% for both node-positive and node-negative cases. For the single informative report of patients with thick tumors (≥4 mm), risk of melanoma-related death was 32.5% for node-positive cases and 30.1% for node-negative cases. For 19 informative case series with any tumor thickness, risk of melanoma-related death ranged from 0% to 47.8% for node-positive cases and from 0% to 13.3% for node-negative cases. CONCLUSION Prognostic information provided by SLNB status may be variably useful for patients who have tumors of intermediate thickness (1-4 mm) and not very useful for patients who have thin (≤1 mm) or thick (≥4 mm) tumors.Arch Dermatol. 2011;147(4):408-415. Published online December 20, 2010. doi:10.1001/archdermatol.2010.371-->
ISSN:0003-987X
2168-6068
1538-3652
2168-6084
DOI:10.1001/archdermatol.2010.371