Cargando…

Update on Epidemiology, Diagnosis, and Biomarkers in Gastroenteropancreatic Neuroendocrine Neoplasms

SIMPLE SUMMARY: Neuroendocrine neoplasms are divided into two groups: well-differentiated neuroendocrine tumors and poorly differentiated neuroendocrine carcinomas. The progress in diagnostic methods, including pathology optimization and imaging, might be one of the reasons for the increasing incide...

Descripción completa

Detalles Bibliográficos
Autores principales: Takayanagi, Daisuke, Cho, Hourin, Machida, Erika, Kawamura, Atsushi, Takashima, Atsuo, Wada, Satoshi, Tsunoda, Takuya, Kohno, Takashi, Shiraishi, Kouya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8909424/
https://www.ncbi.nlm.nih.gov/pubmed/35267427
http://dx.doi.org/10.3390/cancers14051119
Descripción
Sumario:SIMPLE SUMMARY: Neuroendocrine neoplasms are divided into two groups: well-differentiated neuroendocrine tumors and poorly differentiated neuroendocrine carcinomas. The progress in diagnostic methods, including pathology optimization and imaging, might be one of the reasons for the increasing incidence of gastroenteropancreatic neuroendocrine neoplasms; however, the remaining biological factors are undetermined. Rapid advances in molecular diagnostic and treatment strategies in recent years have significantly contributed to personalized management for patients with these rare neoplasms. This review aimed to provide an update on the epidemiology, diagnosis, and biomarkers in gastroenteropancreatic neuroendocrine neoplasms. ABSTRACT: Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) are a heterogeneous group of malignancies that originate from the diffuse neuroendocrine cell system of the pancreas and gastrointestinal tract and have increasingly increased in number over the decades. GEP-NENs are roughly classified into well-differentiated neuroendocrine tumors and poorly differentiated neuroendocrine carcinomas; it is essential to understand the pathological classification according to the mitotic count and Ki67 proliferation index. In addition, with the advent of molecular-targeted drugs and somatostatin analogs and advances in endoscopic and surgical treatments, the multidisciplinary treatment of GEP-NENs has made great progress. In the management of GEP-NENs, accurate diagnosis is key for the proper selection among these diversified treatment methods. The evaluation of hormone-producing ability, diagnostic imaging, and histological diagnosis is central. Advances in the study of the genetic landscape have led to deeper understanding of tumor biology; it has also become possible to identify druggable mutations and predict therapeutic effects. Liquid biopsy, based on blood mRNA expression for GEP-NENs, has been developed, and is useful not only for early detection but also for assessing minimal residual disease after surgery and prediction of therapeutic effects. This review outlines the updates and future prospects of the epidemiology, diagnosis, and management of GEP-NENs.