Young Kate, Iyer Ridhima, Morganstein Daniel, Chau Ian, Cunningham David, Starling Naureen
The Gastrointestinal Unit, The Royal Marsden Hospital NHS Foundation Trust, Fulham Road, London, SW3 6JJ, UK.
Future Oncol. 2015;11(5):853-64. doi: 10.2217/fon.14.285.
Neuroendocrine tumors (NETs) are a rare and heterogeneous group of tumors with widely varying morphologies and behaviors. Due to their rarity and heterogeneity, progress in improving their treatment has been slow. However, in recent years there have been advances both in their characterization and in the available treatment options. This review will attempt to address these, with particular reference to pancreatic NETs. Pancreatic NETs are a subset of NETs, previously known as islet cell tumors, which appear to be a distinct biological entity, responding differently to systemic treatments compared with NETs arising elsewhere in the GI tract.
神经内分泌肿瘤(NETs)是一类罕见且异质性的肿瘤,其形态和行为差异很大。由于其罕见性和异质性,改善其治疗的进展一直缓慢。然而,近年来在其特征描述和可用治疗选择方面都取得了进展。本综述将试图探讨这些问题,尤其涉及胰腺神经内分泌肿瘤。胰腺神经内分泌肿瘤是神经内分泌肿瘤的一个子集,以前称为胰岛细胞瘤,它似乎是一个独特的生物学实体,与起源于胃肠道其他部位的神经内分泌肿瘤相比,对全身治疗的反应不同。