4.4 Article

Genomics of High-Grade Neuroendocrine Neoplasms: Well-Differentiated Neuroendocrine Tumor with High-Grade Features (G3 NET) and Neuroendocrine Carcinomas (NEC) of Various Anatomic Sites

期刊

ENDOCRINE PATHOLOGY
卷 32, 期 1, 页码 192-210

出版社

HUMANA PRESS INC
DOI: 10.1007/s12022-020-09660-z

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High-grade neuroendocrine neoplasms; Neuroendocrine carcinoma; Grade 3 neuroendocrine tumor; Genetics; Genomics; Molecular analysis

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This study redefines high-grade neuroendocrine neoplasms (HG-NENs) by discussing neuroendocrine carcinoma and high proliferating well-differentiated neuroendocrine tumors, providing new diagnostic and therapeutic tools. It systematically analyzes the genomic landscape of HG NENs in various anatomical sites, including common thoracic and digestive locations, as well as rare sites like the skin, head and neck, and urogenital system.
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.

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