| Literature DB >> 30900485 |
Giuseppe Pelosi1,2, Fabrizio Bianchi3, Paul Hofman4, Linda Pattini5, Philipp Ströbel6, Fiorella Calabrese7, Salma Naheed8, Chloe Holden9, Judith Cave10, Hanibal Bohnenberger6, Helen Dinter6, Sergio Harari11, Adriana Albini12, Angelica Sonzogni13, Mauro Papotti14, Marco Volante15, Christian H Ottensmeier16.
Abstract
INTRODUCTION: Neuroendocrine tumors of the lung (Lung-NETs) make up a heterogenous family of neoplasms showing neuroendocrine differentiation and encompass carcinoids and neuroendocrine carcinomas. On molecular grounds, they considered two completely distinct and separate tumor groups with no overlap of molecular alterations nor common developmental mechanisms. Areas covered: Two perspectives were evaluated based on an extensive review and rethinking of literature: (1) the current classification as an instrument to obtaining clinical and molecular insights into the context of Lung-NETs; and (2) an alternative and innovative interpretation of these tumors, proposing a tripartite separation into early aggressive primary high-grade neuroendocrine tumors (HGNET), differentiating or secondary HGNET, and indolent NET. Expert opinion: We herein provide an alternative outlook on Lung-NETs, which is a paradigm shift to current pathogenesis models and expands the understanding of these tumors.Entities:
Keywords: Ki-67 index; Neuroendocrine; carcinoma; copy number variation; evolution; gene; genomic analysis; lung; mutation; pathogenesis; tumor
Mesh:
Substances:
Year: 2019 PMID: 30900485 DOI: 10.1080/14737159.2019.1595593
Source DB: PubMed Journal: Expert Rev Mol Diagn ISSN: 1473-7159 Impact factor: 5.225