Coriat Romain, Walter Thomas, Terris Benoît, Couvelard Anne, Ruszniewski Philippe
Department of Gastroenterology, Cochin Teaching Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France Faculté de Médecine, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Hospices Civils de Lyon, Hôpital Edouard Herriot, Service d'Oncologie Digestive, Lyon Cedex 03, France Université Claude Bernard Lyon 1, Université de Lyon, , Lyon, France.
Oncologist. 2016 Oct;21(10):1191-1199. doi: 10.1634/theoncologist.2015-0476. Epub 2016 Jul 8.
: In 2010, the World Health Organization (WHO) classification of neuroendocrine neoplasms was reviewed and validated the crucial role of the proliferative rate. According to the WHO classification 2010, gastroenteropancreatic neuroendocrine neoplasms are classified as well-differentiated neuroendocrine tumors (NETs) of grade 1 or 2 in up to 84%, or poorly differentiated neuroendocrine carcinomas in 6%-8%. Neuroendocrine carcinomas are of grade G. Recently, a proportion of neuroendocrine tumors presenting a number of mitoses or a Ki-67 index higher than 20% and a well-differentiated morphology have been identified, calling for a new category, well-differentiated grade 3 NET (NET G-3). Studies that have reported the characteristics of neuroendocrine neoplasms have identified more well-differentiated NET G-3 than neuroendocrine carcinomas. The main localizations of NET G-3 are the pancreas, stomach, and colon. Treatment for NET G-3 is not standardized and is balanced between G-1/2 neuroendocrine tumor and neuroendocrine carcinoma treatments. In nonmetastatic neuroendocrine tumors, the European and American guidelines recommended a surgical resection for localized neuroendocrine neoplasm, irrespective of the tumor grading. In NET G-3, chemotherapy is the benchmark if the main treatment goal is reduction of the tumor mass, particularly if it would allow a secondary surgery. In the present work, we review the epidemiology and make recommendations for the management of NET G-3.
Neuroendocrine tumors presenting a number of mitoses or a Ki-67 index higher than 20% and a well-differentiated morphology have been identified and named well-differentiated grade 3 neuroendocrine tumors (NET G-3). The main localizations of NET G-3 are the pancreas, stomach, and colon. The prognosis is worse than that for NET G-2. In nonmetastatic NET G-3, surgery appeared to be the first option. The chemotherapy regimen in pancreatic NET G-3 should be in line with that implemented in NET G-1/2 when the Ki-67 index is below 55% and should be in line with that implemented for neuroendocrine carcinoma when Ki-67 is above 55%.
2010年,世界卫生组织(WHO)对神经内分泌肿瘤的分类进行了审查,并验证了增殖率的关键作用。根据2010年WHO分类,胃肠胰神经内分泌肿瘤高达84%被分类为1级或2级的高分化神经内分泌肿瘤(NETs),6%-8%为低分化神经内分泌癌。神经内分泌癌为G级。最近,已识别出一部分有一定数量核分裂象或Ki-67指数高于20%且形态为高分化的神经内分泌肿瘤,这就需要一个新的类别,即高分化3级NET(NET G-3)。报告神经内分泌肿瘤特征的研究已识别出更多的高分化NET G-3而非神经内分泌癌。NET G-3的主要部位是胰腺、胃和结肠。NET G-3的治疗并不规范,在G-1/2神经内分泌肿瘤和神经内分泌癌的治疗之间取得平衡。在非转移性神经内分泌肿瘤中,欧美指南推荐对局限性神经内分泌肿瘤进行手术切除,无论肿瘤分级如何。在NET G-3中,如果主要治疗目标是缩小肿瘤体积,特别是如果这能允许进行二次手术,化疗是基准治疗方法。在本研究中,我们回顾了NET G-3的流行病学并对其管理提出建议。
已识别出有一定数量核分裂象或Ki-67指数高于20%且形态为高分化的神经内分泌肿瘤,并将其命名为高分化3级神经内分泌肿瘤(NET G-3)。NET G-3的主要部位是胰腺、胃和结肠。其预后比NET G-2差。在非转移性NET G-3中,手术似乎是首选。当Ki-67指数低于55%时,胰腺NET G-3的化疗方案应与NET G-1/2中实施的方案一致;当Ki-67高于55%时,应与神经内分泌癌的化疗方案一致。