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Originally published as JCO Early Release 10.1200/JCO.2008.19.0033 on September 8 2009

Journal of Clinical Oncology, Vol 27, No 30 (October 20), 2009: pp. 4994-5000
© 2009 American Society of Clinical Oncology.

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Melanoma

Rotterdam Criteria for Sentinel Node (SN) Tumor Burden and the Accuracy of Ultrasound (US) -Guided Fine-Needle Aspiration Cytology (FNAC): Can US-Guided FNAC Replace SN Staging in Patients With Melanoma?

Christiane A. Voit, Alexander C.J. van Akkooi, Gregor Schäfer-Hesterberg, Alfred Schoengen, Paul I.M. Schmitz, Wolfram Sterry, Alexander M.M. Eggermont

From the Department of Dermatology, Charité, Humboldt University, Berlin; Department of Medical Oncology, Armed Forces Hospital, University of Ulm, Ulm, Germany; and Departments of Surgical Oncology and Statistics, Erasmus University Medical Center–Daniel den Hoed Cancer Center, the Netherlands.

Corresponding author: Christiane Voit, MD, Department of Dermatology, Charité, Humboldt University, Berlin, Schumannstr 20/21, 10117 Berlin, Germany; e-mail: christiane.voit{at}t-online.de.

Purpose Sentinel node (SN) status is the most important prognostic factor for overall survival (OS) for patients with stage I/II melanoma, and the role of the SN procedure as a staging procedure has long been established. However, a less invasive procedure, such as ultrasound (US) -guided fine-needle aspiration cytology (FNAC), would be preferred. The aim of this study was to evaluate the accuracy of US-guided FNAC and compare the results with histology after SN surgery was performed in all patients.

Patients and Methods Four hundred consecutive patients who underwent lymphoscintigraphy subsequently underwent a US examination before the SN procedure. When the US examination showed a suspicious or malignant pattern, patients underwent an FNAC. Median Breslow thickness was 1.8 mm; mean follow-up was 42 months (range, 4 to 82 months). We considered the US-guided FNAC positive if either US and/or FNAC were positive. If US was suggestive of abnormality, but FNAC was negative, the US-guided FNAC was considered negative.

Results US-guided FNAC identified 51 (65%) of 79 SN metastases. Specificity was 99% (317 of 321), with a positive predictive value of 93% and negative predictive value of 92%. SN-positive identification rate by US-guided FNAC increased from 40% in stage pT1a/b disease to 79% in stage pT4a/b disease. US-guided FNAC detected SN tumors more than 1.0 mm in 86% of cases, SN tumors of 0.1 to 1.0 mm in 46% of cases, and SN tumors less than 0.1 mm in 23% of cases. Estimated 5-year OS rates were 92% for patients with negative US-guided FNAC results and 51% for patients with positive results.

Conclusion US-guided FNAC of SNs is highly accurate. Up to 65% of the patients with SN-positive results in our institution could have been spared an SN procedure.

Both C.A.V. and A.C.J.v.A. contributed equally to this work.

Supported by Deutsche Krebshilfe (Grant No. 70-2791-Vo I).

Authors' disclosures of potential conflicts of interest and author contributions are found at the end of this article.


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Copyright © 2009 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
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