Department of General, Minimally Invasive and Endocrine Surgery, Wroclaw Medical University, Poland.
Pol Przegl Chir. 2024 Mar 8;96(4):58-66. doi: 10.5604/01.3001.0054.4169.
<b>Introduction:</b> Gastro-entero-pancreatic neuroendocrine neoplasms (GEP-NENs) are malignancies originating from cells of the diffuse endocrine system. They are rare and localize in the upper and lower parts of the gastrointestinal tract and in the pancreas. Despite such a varied location, GEP-NENs are considered a common group of neoplasms due to the fact of their similar morphology and ability to secrete peptide hormones and biologically active amines. They are associated with clinical manifestations specific to the substances produced by a particular neoplasm. The classification of GEP-NENs is constantly systematized and updated based on their differentiation and grading. The development of available diagnostic and treatment methods for these tumors has made significant progress over the past 10 years and is still ongoing.<b>Aim:</b> In the following paper, we review the diagnostics and treatment of GEP-NENs, taking into account the latest molecular, immunological, or gene-based methods. Imaging methods using markers for receptors allow for high diagnostic sensitivity<b>Methods:</b> Medical databases were searched for the latest information. The authors also sought confirmation of the content of a particular publication in another publications, so as to present the most reliable information possible.<b>Results:</b> Research results revealed that the diagnostics and treatment of GEP-NENs have significantly advanced in recent years. Surgical interventions, especially minimally invasive techniques, have shown efficacy in treating GEP-NENs, with specific therapies such as somatostatin analogs, chemotherapy, and peptide receptor radionuclide therapy demonstrating promising outcomes. The evolution of diagnostic methods, including imaging techniques and biomarker testing, has contributed to improved patient care and prognosis.<b>Conclusions:</b> The increasing incidence of GEP-NENs is attributed to enhanced diagnostic capabilities rather than a rise in population prevalence. The study emphasizes the importance of ongoing research to identify specific markers for early detection and targeted therapies to further enhance the effectiveness of treating these rare and heterogeneous malignancies. The findings suggest a positive trajectory in the management of GEP-NENs, with future prospects focused on personalized and targeted treatment approaches.
胃-肠-胰腺神经内分泌肿瘤(GEP-NENs)起源于弥散内分泌系统的细胞,属于恶性肿瘤。它们较为罕见,定位于胃肠道的上下部分和胰腺。尽管这些肿瘤的位置各不相同,但由于其形态相似,且具有分泌肽类激素和生物活性胺的能力,因此被视为一类常见的肿瘤。这些肿瘤与特定肿瘤产生的物质所导致的临床表现相关。GEP-NEN 的分类不断系统化和更新,基于其分化和分级。在过去的 10 年中,针对这些肿瘤的诊断和治疗方法有了显著进展,并且仍在不断发展。目的:在本文中,我们回顾了 GEP-NEN 的诊断和治疗方法,同时考虑了最新的分子、免疫或基因方法。使用受体标志物的成像方法可实现高诊断灵敏度。方法:在医学数据库中搜索最新信息。作者还寻求在其他出版物中确认特定出版物的内容,以提供尽可能可靠的信息。结果:研究结果表明,近年来 GEP-NEN 的诊断和治疗取得了显著进展。外科干预,尤其是微创技术,已被证明在治疗 GEP-NEN 方面有效,具体的治疗方法,如生长抑素类似物、化疗和肽受体放射性核素治疗,显示出了良好的效果。诊断方法的发展,包括成像技术和生物标志物检测,有助于改善患者的护理和预后。结论:GEP-NEN 发病率的增加归因于诊断能力的提高,而不是人口流行率的上升。本研究强调了持续研究的重要性,以确定用于早期检测的特定标志物和靶向治疗方法,从而进一步提高治疗这些罕见和异质性恶性肿瘤的效果。研究结果表明,GEP-NEN 的管理呈积极态势,未来的前景集中在个性化和靶向治疗方法上。