TY - JOUR
T1 - Genomics of High-Grade Neuroendocrine Neoplasms
T2 - Well-Differentiated Neuroendocrine Tumor with High-Grade Features (G3 NET) and Neuroendocrine Carcinomas (NEC) of Various Anatomic Sites
AU - Uccella, Silvia
AU - La Rosa, Stefano
AU - Metovic, Jasna
AU - Marchiori, Deborah
AU - Scoazec, Jean Yves
AU - Volante, Marco
AU - Mete, Ozgur
AU - Papotti, Mauro
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature.
PY - 2021/3/1
Y1 - 2021/3/1
N2 - High-grade neuroendocrine neoplasms (HG-NENs) are clinically aggressive diseases, the classification of which has recently been redefined. They now include both poorly differentiated NENs (neuroendocrine carcinoma, NECs) and high proliferating well-differentiated NENs (called grade 3 neuroendocrine tumors, G3 NETs, in the digestive system). In the last decade, the “molecular revolution” that has affected all fields of medical oncology has also shed light in the understanding of HG NENs heterogeneity and has provided new diagnostic and therapeutic tools, useful in the management of these malignancies. Considering the kaleidoscopic aspects of HG NENs in various anatomical sites, this review systematically addresses the genomic landscape of such neoplasm throughout the more common thoracic and digestive locations, as well as it will consider other rare but not exceptional primary sites, including the skin, the head and neck, and the urogenital system. The revision of the available literature will then be oriented to understand the translational relevance of molecular data, by analyzing conceptual issues, clinicopathological correlations, and unmet needs in this field.
AB - High-grade neuroendocrine neoplasms (HG-NENs) are clinically aggressive diseases, the classification of which has recently been redefined. They now include both poorly differentiated NENs (neuroendocrine carcinoma, NECs) and high proliferating well-differentiated NENs (called grade 3 neuroendocrine tumors, G3 NETs, in the digestive system). In the last decade, the “molecular revolution” that has affected all fields of medical oncology has also shed light in the understanding of HG NENs heterogeneity and has provided new diagnostic and therapeutic tools, useful in the management of these malignancies. Considering the kaleidoscopic aspects of HG NENs in various anatomical sites, this review systematically addresses the genomic landscape of such neoplasm throughout the more common thoracic and digestive locations, as well as it will consider other rare but not exceptional primary sites, including the skin, the head and neck, and the urogenital system. The revision of the available literature will then be oriented to understand the translational relevance of molecular data, by analyzing conceptual issues, clinicopathological correlations, and unmet needs in this field.
KW - Genetics
KW - Genomics
KW - Grade 3 neuroendocrine tumor
KW - High-grade neuroendocrine neoplasms
KW - Molecular analysis
KW - Neuroendocrine carcinoma
UR - http://www.scopus.com/inward/record.url?scp=85099344223&partnerID=8YFLogxK
U2 - 10.1007/s12022-020-09660-z
DO - 10.1007/s12022-020-09660-z
M3 - Review article
C2 - 33433884
AN - SCOPUS:85099344223
SN - 1046-3976
VL - 32
SP - 192
EP - 210
JO - Endocrine Pathology
JF - Endocrine Pathology
IS - 1
ER -