Digestive Disease Unit, ENETS Center of Excellence, Sant'Andrea University Hospital, Sapienza University of Rome, Rome, Italy.
Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
Endocrine. 2023 Nov;82(2):435-441. doi: 10.1007/s12020-023-03418-3. Epub 2023 Jun 20.
Histological evaluation and grading assessment are key points in the diagnostic work-up of gastroentero-pancreatic neuroendocrine neoplasms (GEP-NENs).
To analyze the impact of histopathological revision on the clinical management of patients with GEP-NEN.
Patients referred to our Center of Excellence between 2015 and 2021 were included in this study. Immunohistochemical slides at the time of initial diagnosis were reviewed to assess tumor morphology, diagnostic immunohistochemistry, and Ki67.
101 patients were evaluated, with 65 (64.4%) gastrointestinal, 25 (24.7%) pancreatic, and 11 (10.9%) occult neoplastic lesions suspected to be of GEP origin. The main changes resulting from the revision were: first Ki-67 assessment in 15.8% of patients, Ki-67 change in 59.2% of patients and grading modification in 23.5% of patients. An additional immunohistochemical evaluation was performed in 78 (77.2%) patients, leading to a confirmation of GEP origin in 10 of 11 (90.9%) of unknown primary site neoplastic lesions and an exclusion of NEN diagnosis in 2 (2%) patients. After histopathological revision, a significant modification in clinical management was proposed in 42 (41.6%) patients.
Histopathological revision in a referral NEN center is strongly advised in newly diagnosed GEP-NENs to properly plan prognostic stratification and therapeutic choice.
组织学评估和分级评估是胃肠胰神经内分泌肿瘤(GEP-NENs)诊断工作的重点。
分析病理组织学修订对 GEP-NEN 患者临床管理的影响。
本研究纳入了 2015 年至 2021 年期间我院卓越中心收治的患者。回顾初始诊断时的免疫组化切片,评估肿瘤形态、诊断免疫组化和 Ki67。
共评估了 101 例患者,其中 65 例(64.4%)为胃肠道、25 例(24.7%)为胰腺、11 例(10.9%)为隐匿性疑似 GEP 起源的肿瘤病变。修订后主要的变化包括:首次 Ki-67 评估占 15.8%,59.2%的患者 Ki-67 改变,23.5%的患者分级修改。对 78 例(77.2%)患者进行了额外的免疫组化评估,导致 11 例(90.9%)未知原发部位肿瘤病变明确为 GEP 起源,2 例(2%)患者排除 NEN 诊断。病理组织学修订后,42 例(41.6%)患者的临床管理方案发生了显著改变。
强烈建议在新诊断的 GEP-NEN 中对病理组织学进行修订,以正确规划预后分层和治疗选择。