• David S Klimstra, Irvin R Modlin, N Volkan Adsay, Runjan Chetty, Vikram Deshpande, Mithat Gönen, Robert T Jensen, Mark Kidd, Matthew H Kulke, Ricardo V Lloyd, Cesar Moran, Steven F Moss, Kjell Oberg, Dermot O'Toole, Guido Rindi, Marie E Robert, Saul Suster, Laura H Tang, Chin-Yuan Tzen, Mary Kay Washington, Betram Wiedenmann, and James Yao.
• Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA. klimstrd@mskcc.org
• Am. J. Surg. Pathol. 2010 Mar 1; 34 (3): 300-13.

AbstractEpithelial neuroendocrine tumors (NETs) have been the subject of much debate regarding their optimal classification. Although multiple systems of nomenclature, grading, and staging have been proposed, none has achieved universal acceptance. To help define the underlying common features of these classification systems and to identify the minimal pathology data that should be reported to ensure consistent clinical management and reproducibility of data from therapeutic trials, a multidisciplinary team of physicians interested in NETs was assembled. At a group meeting, the participants discussed a series of "yes" or "no" questions related to the pathology of NETs and the minimal data to be included in the reports. After discussion, anonymous votes were taken, using the Delphic principle that 80% agreement on a vote of either yes or no would define a consensus. Questions that failed to achieve a consensus were rephrased once or twice and discussed, and additional votes were taken. Of 108 questions, 91 were answerable either yes or no by more than 80% of the participants. There was agreement about the importance of proliferation rate for tumor grading, the landmarks to use for staging, the prognostic factors assessable by routine histology that should be reported, the potential for tumors to progress biologically with metastasis, and the current status of advanced immunohistochemical and molecular testing for treatment-related biomarkers. The lack of utility of a variety of immunohistochemical stains and pathologic findings was also agreed upon. A consensus could not be reached for the remaining 17 questions, which included both minor points related to extent of disease assessment and some major areas such as terminology, routine immunohistochemical staining for general neuroendocrine markers, use of Ki67 staining to assess proliferation, and the relationship of tumor grade to degree of differentiation. On the basis of the results of the Delphic voting, a minimum pathology data set was developed. Although there remains disagreement among experts about the specific classification system that should be used, there is agreement about the fundamental pathology data that should be reported. Examination of the areas of disagreement reveals significant opportunities for collaborative study to resolve unanswered questions.

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