Strosberg Jonathan R, Halfdanarson Thorvardur R, Bellizzi Andrew M, Chan Jennifer A, Dillon Joseph S, Heaney Anthony P, Kunz Pamela L, O'Dorisio Thomas M, Salem Riad, Segelov Eva, Howe James R, Pommier Rodney F, Brendtro Kari, Bashir Mohammad A, Singh Simron, Soulen Michael C, Tang Laura, Zacks Jerome S, Yao James C, Bergsland Emily K
From the *Department of GI Oncology, H. Lee Moffitt Cancer Center, Tampa FL; †Division of Medical Oncology, Mayo Clinic, Rochester, MN; ‡Department of Pathology, University of Iowa, Iowa City, IA; §Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA; ∥Department of Medicine, University of Iowa, Iowa City, IA; ¶Departments of Medicine and Neurosurgery, University of California Los Angeles, Los Angeles; and #Department of Medicine, Division of Oncology, Stanford University School of Medicine, Stanford, CA; **Department of Radiology, Northwestern University, Chicago IL; ††Department of Oncology, Monash University and Monash Health, Melbourne, Victoria, Australia; ‡‡Department of Surgery, University of Iowa Carver College of Medicine, Iowa City, IA; §§Oregon Health & Science University and ∥∥North American Neuroendocrine Tumor Society, Portland, OR; ¶¶Division of Cardiothoracic Surgery, Department of Surgery, University of Iowa Carver College of Medicine, Iowa City, IA; ##Sunnybrook Hospital, Toronto, Canada; ***Department of Radiology, University of Pennsylvania, Philadelphia, PA; †††Memorial Sloan Kettering University and ‡‡‡Division of Cardiology, Mount Sinai Hospital, New York, NY; §§§Department of Gastrointestinal Medical Oncology, MD Anderson Cancer Center, Houston TX; and ∥∥∥Department of Medicine, University of California San Francisco, San Francisco, CA.
Pancreas. 2017 Jul;46(6):707-714. doi: 10.1097/MPA.0000000000000850.
There have been significant developments in diagnostic and therapeutic options for patients with neuroendocrine tumors (NETs). Key phase 3 studies include the CLARINET trial, which evaluated lanreotide in patients with nonfunctioning enteropancreatic NETs; the RADIANT-2 and RADIANT-4 studies, which evaluated everolimus in functioning and nonfunctioning NETs of the gastrointestinal tract and lungs; the TELESTAR study, which evaluated telotristat ethyl in patients with refractory carcinoid syndrome; and the NETTER-1 trial, which evaluated Lu-DOTATATE in NETs of the small intestine and proximal colon (midgut). Based on these and other advances, the North American Neuroendocrine Tumor Society convened a multidisciplinary panel of experts with the goal of updating consensus-based guidelines for evaluation and treatment of midgut NETs. The medical aspects of these guidelines (focusing on systemic treatment, nonsurgical liver-directed therapy, and postoperative surveillance) are summarized in this article. Surgical guidelines are described in a companion article.
神经内分泌肿瘤(NETs)患者的诊断和治疗选择有了重大进展。关键的3期研究包括CLARINET试验,该试验评估了兰瑞肽在无功能性胃肠胰神经内分泌肿瘤患者中的应用;RADIANT-2和RADIANT-4研究,评估了依维莫司在胃肠道和肺部功能性和无功能性神经内分泌肿瘤中的应用;TELESTAR研究,评估了乙基色氨酸在难治性类癌综合征患者中的应用;以及NETTER-1试验,评估了镥[177Lu]奥曲肽在小肠和近端结肠(中肠)神经内分泌肿瘤中的应用。基于这些及其他进展,北美神经内分泌肿瘤协会召集了一个多学科专家小组,目标是更新基于共识的中肠神经内分泌肿瘤评估和治疗指南。本文总结了这些指南的医学方面内容(重点是全身治疗、非手术肝脏定向治疗和术后监测)。手术指南在另一篇配套文章中进行了描述。