Modlin Irvin M, Oberg Kjell, Chung Daniel C, Jensen Robert T, de Herder Wouter W, Thakker Rajesh V, Caplin Martyn, Delle Fave Gianfranco, Kaltsas Greg A, Krenning Eric P, Moss Steven F, Nilsson Ola, Rindi Guido, Salazar Ramon, Ruszniewski Philippe, Sundin Anders
Department of Gastroenterological Surgery, Yale University, New Haven, CT 06520-8062, USA.
Lancet Oncol. 2008 Jan;9(1):61-72. doi: 10.1016/S1470-2045(07)70410-2.
Gastroenteropancreatic (GEP) neuroendocrine tumours (NETs) are fairly rare neoplasms that present many clinical challenges. They secrete peptides and neuroamines that cause distinct clinical syndromes, including carcinoid syndrome. However, many are clinically silent until late presentation with mass effects. Investigation and management should be highly individualised for a patient, taking into consideration the likely natural history of the tumour and general health of the patient. Management strategies include surgery for cure (which is achieved rarely) or for cytoreduction, radiological intervention (by chemoembolisation and radiofrequency ablation), chemotherapy, and somatostatin analogues to control symptoms that result from release of peptides and neuroamines. New biological agents and somatostatin-tagged radionuclides are under investigation. The complexity, heterogeneity, and rarity of GEP NETs have contributed to a paucity of relevant randomised trials and little or no survival increase over the past 30 years. To improve outcome from GEP NETs, a better understanding of their biology is needed, with emphasis on molecular genetics and disease modeling. More-reliable serum markers, better tumour localisation and identification of small lesions, and histological grading systems and classifications with prognostic application are needed. Comparison between treatments is currently very difficult. Progress is unlikely to occur without development of centers of excellence, with dedicated combined clinical teams to coordinate multicentre studies, maintain clinical and tissue databases, and refine molecularly targeted therapeutics.
胃肠胰(GEP)神经内分泌肿瘤(NETs)是相当罕见的肿瘤,带来了许多临床挑战。它们分泌肽类和神经胺类物质,可导致包括类癌综合征在内的独特临床综合征。然而,许多肿瘤在出现占位效应之前临床上并无症状。对患者的检查和管理应高度个体化,要考虑到肿瘤可能的自然病程以及患者的总体健康状况。管理策略包括旨在治愈的手术(很少能实现)或减瘤手术、放射介入治疗(通过化疗栓塞和射频消融)、化疗以及使用生长抑素类似物来控制因肽类和神经胺类物质释放而产生的症状。新型生物制剂和生长抑素标记的放射性核素正在研究中。GEP NETs的复杂性、异质性和罕见性导致相关随机试验较少,并且在过去30年中生存率几乎没有提高。为改善GEP NETs的治疗效果,需要更好地了解其生物学特性,重点是分子遗传学和疾病建模。还需要更可靠的血清标志物、更好的肿瘤定位以及对小病变的识别,以及具有预后应用价值的组织学分级系统和分类方法。目前很难对不同治疗方法进行比较。如果没有卓越中心的发展,配备专门的联合临床团队来协调多中心研究、维护临床和组织数据库并优化分子靶向治疗,就不太可能取得进展。