O'Connor Juan Manuel, Marmissolle Fabiana, Bestani Claudia, Pesce Veronica, Belli Susana, Dominichini Enzo, Mendez Guillermo, Price Paola, Giacomi Nora, Pairola Alejandro, Loria Fernando Sánchez, Huertas Eduardo, Martin Claudio, Patane Karina, Poleri Claudia, Rosenberg Moises, Cabanne Ana, Kujaruk Mirta, Caino Analia, Zamora Victor, Mariani Javier, Dioca Mariano, Parma Patricia, Podesta Gustavo, Andriani Oscar, Gondolesi Gabriel, Roca Enrique
Department of Clinical Oncology, Institute Alexander Fleming, Buenos Aires C1426ANZ, Argentina ; Oncology Unit, Gastroenterology Hospital Bonorino Udaondo, Buenos Aires C1264AAA, Argentina.
SITE, Clinical Oncology, La Plata 1900, Argentina ; Medical Institute Platense, Buenos Aires 1900, Argentina.
Mol Clin Oncol. 2014 Sep;2(5):673-684. doi: 10.3892/mco.2014.332. Epub 2014 Jun 27.
Neuroendocrine tumors (NET) include a spectrum of malignancies arising from neuroendocrine cells throughout the body. The objective of this clinical investigation of retrospectively and prospectively collected data was to describe the prevalence, demographic data, clinical symptoms and methods of diagnosis of NET and the treatment and long-term follow-up of patients with NET. Data were provided by the participating centers and assessed for consistency by internal reviewers. All the cases were centrally evaluated (when necessary) by the pathologists in our group. The tissue samples were reviewed by hematoxylin and eosin and immunohistochemical staining techniques to confirm the diagnosis of NET. In total, 532 cases were documented: 461 gastroenteropancreatic-NET (GEP-NET) and 71 bronchial NET (BNET). All the tumors were immunohistochemically defined according to the World Health Organization (WHO) and European Neuroendocrine Tumor Society criteria. The most common initial symptoms in GEP-NET were abdominal pain, diarrhea, bowel obstruction, flushing, gastrointestinal bleeding and weight loss. The most common tumor types were carcinoid (58.0%), non-functional pancreatic tumor (23.0%), metastatic NET of unknown primary (16.0%) and functional pancreatic tumor (3.0%). Of the BNET, 89.0% were typical and 11.0% atypical carcinoids. Of the patients with GEP-NET, 59.2% had distant metastasis at diagnosis. The locations of the primary tumors in GEP-NET were the small bowel (26.9%), pancreas (25.2%), colon-rectum (12.4%), appendix (7.6%), stomach (6.9%), esophagus (2.8%), duodenum (2.0%) and unknown primary (16.3%). The histological subtypes based on the WHO classification were well-differentiated NET (20.1%), well-differentiated neuroendocrine carcinomas (66.5%) and poorly differentiated neuroendocrine carcinomas (10.3%). Overall, 67.3% of the patients underwent surgery, 41.2% with curative intent and 26.1% for palliative purposes. The 5-year survival rates were 65.1% (95% confidence interval, 58.0-71.4%) in GEP-NET and 100.0% in typical carcinoid of the lung. This observational, non-interventional, longitudinal study aimed to accumulate relevant information regarding the epidemiology, clinical presentation and current practices in the treatment of NET patients in Argentina, providing insight into regional differences and patterns of care in this heterogeneous disease.
神经内分泌肿瘤(NET)包括一系列起源于全身神经内分泌细胞的恶性肿瘤。这项对回顾性和前瞻性收集的数据进行的临床研究的目的是描述NET的患病率、人口统计学数据、临床症状、诊断方法以及NET患者的治疗和长期随访情况。数据由参与研究的中心提供,并由内部审核人员评估其一致性。所有病例在必要时由我们团队的病理学家进行集中评估。通过苏木精-伊红染色和免疫组织化学染色技术对组织样本进行复查,以确诊NET。总共记录了532例病例:461例胃肠胰神经内分泌肿瘤(GEP-NET)和71例支气管神经内分泌肿瘤(BNET)。所有肿瘤均根据世界卫生组织(WHO)和欧洲神经内分泌肿瘤学会的标准进行免疫组织化学定义。GEP-NET最常见的初始症状为腹痛、腹泻、肠梗阻、潮红、胃肠道出血和体重减轻。最常见的肿瘤类型为类癌(58.0%)、无功能胰腺肿瘤(23.0%)、原发灶不明的转移性NET(16.0%)和功能性胰腺肿瘤(3.0%)。在BNET中,89.0%为典型类癌,11.0%为非典型类癌。GEP-NET患者中,59.2%在诊断时已有远处转移。GEP-NET原发肿瘤的部位为小肠(26.9%)、胰腺(25.2%)、结肠-直肠(12.4%)、阑尾(7.6%)、胃(6.9%)、食管(2.8%)、十二指肠(2.0%)以及原发灶不明(16.3%)。根据WHO分类的组织学亚型为高分化NET(20.1%)、高分化神经内分泌癌(66.5%)和低分化神经内分泌癌(10.3%)。总体而言,67.3%的患者接受了手术,其中41.2%为根治性手术,26.1%为姑息性手术。GEP-NET的5年生存率为65.1%(95%置信区间,58.0 - 71.4%),肺典型类癌的5年生存率为100.0%。这项观察性、非干预性的纵向研究旨在积累有关阿根廷NET患者的流行病学、临床表现和当前治疗实践的相关信息,深入了解这种异质性疾病的地区差异和护理模式。