Modern Management of Gastric Neuroendocrine Neoplasms.

IF 3.8 2区 医学 Q2 ONCOLOGY
Current Treatment Options in Oncology Pub Date : 2024-09-01 Epub Date: 2024-07-31 DOI:10.1007/s11864-024-01207-2
John W Kunstman, Anil Nagar, Joanna Gibson, Pamela L Kunz
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引用次数: 0

Abstract

Opinion statement: Gastric neuroendocrine neoplasms (G-NENs) are a heterogeneous group of tumors that broadly fall into two groups. The first group, driven by oversecretion of gastrin, are generally multifocal, small, and behave indolently with a low (but non-zero) risk of progression and metastatic spread. They are conventionally categorized into type 1, with endogenous gastric-based overproduction of gastrin, and type 2 G-NEN, with overproduction of gastrin from an extra-gastric gastrin-secreting tumor. The second group, termed type 3 G-NEN, occur spontaneously and are potentially more aggressive, having a clinical course analogous to other neuroendocrine tumors of the gastrointestinal tract. Type 1 G-NEN can be managed with endoscopic surveillance and resection of visible lesions with great success, reserving surgery for the rare high-risk lesion, whereas surgical resection of the causative gastrin-secreting tumor in type 2 G-NEN is usually curative. Type 3 G-NEN is usually managed with formal surgical resection but there is growing evidence that limited surgery or even endoscopic resection in appropriately selected patients with low risk is both safe and effective. A novel subtype of G-NEN, associated with long-term proton pump inhibitor usage, is increasing in incidence. The pathophysiology seems to parallel type 1 G-NEN. In the setting of metastatic disease, which can occur in any subtype but is most common by far in type 3 G-NEN, the lack of trial data unique to G-NEN results in extrapolation of strategies and agents for treatment of non-gastric neuroendocrine disease. The rapid pace of development in this area is likely to benefit the metastatic G-NEN patient as well. As treatment is predicate on type of G-NEN, establishing the etiology of the lesion is crucial but growing knowledge of G-NEN pathophysiology and close collaboration between pathologists, gastroenterologists, radiologists, surgeons, and oncologists have enabled a growing trend towards de-escalation and less-invasive treatment paradigms.

Abstract Image

胃神经内分泌肿瘤的现代治疗。
意见陈述:胃神经内分泌肿瘤(G-NENs)是一类异质性肿瘤,大致可分为两类。第一类是由胃泌素分泌过多引起的肿瘤,一般为多灶性,体积小,表现不明显,进展和转移风险低(但并非零)。传统上将其分为 1 型和 2 型,前者是内源性胃源性胃泌素分泌过多,后者是由胃外胃泌素分泌肿瘤引起的胃泌素分泌过多。第二类称为 3 型 G-NEN,是自发性的,可能更具侵袭性,其临床过程类似于胃肠道的其他神经内分泌肿瘤。1 型 G-NEN 可通过内镜监测和切除可见病灶来治疗,效果很好,只有极少数高危病灶才会进行手术,而 2 型 G-NEN 的致病性胃泌素分泌瘤的手术切除通常可以治愈。3 型 G-NEN 通常采用正式的手术切除,但越来越多的证据表明,对适当选择的低风险患者进行有限的手术甚至内镜切除既安全又有效。与长期服用质子泵抑制剂有关的一种新型 G-NEN 亚型的发病率正在上升。其病理生理学似乎与 1 型 G-NEN 相似。转移性疾病可发生于任何亚型,但迄今为止在 3 型 G-NEN 中最为常见,由于缺乏 G-NEN 独有的试验数据,因此需要外推治疗非胃神经内分泌疾病的策略和药物。这一领域的快速发展很可能也会使转移性 G-NEN 患者受益。由于治疗取决于 G-NEN 的类型,因此确定病变的病因至关重要,但由于对 G-NEN 病理生理学的认识不断加深,病理学家、胃肠病学家、放射学家、外科医生和肿瘤学家之间的密切合作,使得降级和微创治疗范例日益成为趋势。
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来源期刊
CiteScore
7.10
自引率
0.00%
发文量
113
审稿时长
>12 weeks
期刊介绍: This journal aims to review the most important, recently published treatment option advances in the field of oncology. By providing clear, insightful, balanced contributions by international experts, the journal intends to facilitate worldwide approaches to cancer treatment. We accomplish this aim by appointing international authorities to serve as Section Editors in key subject areas, such as endocrine tumors, lymphomas, neuro-oncology, and cancers of the breast, head and neck, lung, skin, gastrointestinal tract, and genitourinary region. Section Editors, in turn, select topics for which leading experts contribute comprehensive review articles that emphasize new developments and recently published papers of major importance, highlighted by annotated reference lists. We also provide commentaries from well-known oncologists, and an international Editorial Board reviews the annual table of contents, suggests articles of special interest to their country/region, and ensures that topics are current and include emerging research.
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