TY - JOUR
T1 - A common classification framework for neuroendocrine neoplasms
T2 - an International Agency for Research on Cancer (IARC) and World Health Organization (WHO) expert consensus proposal
AU - Rindi, Guido
AU - Klimstra, David S.
AU - Abedi-Ardekani, Behnoush
AU - Asa, Sylvia L.
AU - Bosman, Frederik T.
AU - Brambilla, Elisabeth
AU - Busam, Klaus J.
AU - de Krijger, Ronald R.
AU - Dietel, Manfred
AU - El-Naggar, Adel K.
AU - Fernandez-Cuesta, Lynnette
AU - Klöppel, Günter
AU - McCluggage, W. Glenn
AU - Moch, Holger
AU - Ohgaki, Hiroko
AU - Rakha, Emad A.
AU - Reed, Nicholas S.
AU - Rous, Brian A.
AU - Sasano, Hironobu
AU - Scarpa, Aldo
AU - Scoazec, Jean Yves
AU - Travis, William D.
AU - Tallini, Giovanni
AU - Trouillas, Jacqueline
AU - van Krieken, J. Han
AU - Cree, Ian A.
N1 - Publisher Copyright:
© 2018, United States & Canadian Academy of Pathology.
PY - 2018/12/1
Y1 - 2018/12/1
N2 - The classification of neuroendocrine neoplasms (NENs) differs between organ systems and currently causes considerable confusion. A uniform classification framework for NENs at any anatomical location may reduce inconsistencies and contradictions among the various systems currently in use. The classification suggested here is intended to allow pathologists and clinicians to manage their patients with NENs consistently, while acknowledging organ-specific differences in classification criteria, tumor biology, and prognostic factors. The classification suggested is based on a consensus conference held at the International Agency for Research on Cancer (IARC) in November 2017 and subsequent discussion with additional experts. The key feature of the new classification is a distinction between differentiated neuroendocrine tumors (NETs), also designated carcinoid tumors in some systems, and poorly differentiated NECs, as they both share common expression of neuroendocrine markers. This dichotomous morphological subdivision into NETs and NECs is supported by genetic evidence at specific anatomic sites as well as clinical, epidemiologic, histologic, and prognostic differences. In many organ systems, NETs are graded as G1, G2, or G3 based on mitotic count and/or Ki-67 labeling index, and/or the presence of necrosis; NECs are considered high grade by definition. We believe this conceptual approach can form the basis for the next generation of NEN classifications and will allow more consistent taxonomy to understand how neoplasms from different organ systems inter-relate clinically and genetically.
AB - The classification of neuroendocrine neoplasms (NENs) differs between organ systems and currently causes considerable confusion. A uniform classification framework for NENs at any anatomical location may reduce inconsistencies and contradictions among the various systems currently in use. The classification suggested here is intended to allow pathologists and clinicians to manage their patients with NENs consistently, while acknowledging organ-specific differences in classification criteria, tumor biology, and prognostic factors. The classification suggested is based on a consensus conference held at the International Agency for Research on Cancer (IARC) in November 2017 and subsequent discussion with additional experts. The key feature of the new classification is a distinction between differentiated neuroendocrine tumors (NETs), also designated carcinoid tumors in some systems, and poorly differentiated NECs, as they both share common expression of neuroendocrine markers. This dichotomous morphological subdivision into NETs and NECs is supported by genetic evidence at specific anatomic sites as well as clinical, epidemiologic, histologic, and prognostic differences. In many organ systems, NETs are graded as G1, G2, or G3 based on mitotic count and/or Ki-67 labeling index, and/or the presence of necrosis; NECs are considered high grade by definition. We believe this conceptual approach can form the basis for the next generation of NEN classifications and will allow more consistent taxonomy to understand how neoplasms from different organ systems inter-relate clinically and genetically.
UR - http://www.scopus.com/inward/record.url?scp=85052912604&partnerID=8YFLogxK
U2 - 10.1038/s41379-018-0110-y
DO - 10.1038/s41379-018-0110-y
M3 - Article
C2 - 30140036
AN - SCOPUS:85052912604
SN - 0893-3952
VL - 31
SP - 1770
EP - 1786
JO - Modern Pathology
JF - Modern Pathology
IS - 12
ER -