Department of Nuclear Medicine and Molecular Imaging, Singapore General Hospital, Singapore, Singapore.
Duke-NUS Medical School, Singapore, Singapore.
J Neuroendocrinol. 2023 Dec;35(12):e13349. doi: 10.1111/jne.13349. Epub 2023 Nov 8.
Despite advances in diagnosis and management, patients with advanced pheochromocytomas and paragangliomas (PPGL) face limited treatment options. This study aims to evaluate the safety and efficacy of peptide receptor radionuclide therapy (PRRT) in patients with advanced PPGL, based on a single-institution experience and provide a comprehensive review of the literature.
A retrospective analysis was conducted on patients with advanced pheochromocytoma and paraganglioma who received PRRT at a single institution from April 2012 to March 2022. Clinical characteristics, treatment response, adverse events, and survival outcomes were assessed. A systematic literature review was also performed.
A total of 15 patients with advanced PPGL were included, the majority of whom had both metastatic and functional disease. Most patients received four infusions of 177Lu-DOTATATE (73%). The median therapeutic 177Lu-DOTATATE radioactivity for each infusion was 7.4 GBq. Only one patient was treated with one infusion of 90Y-DOTATATE (4.2 GBq) in addition to three infusions of Lu-177 DOTATATE. Overall, PRRT suggests a promising efficacy with disease control rate of 63.6% by RECIST v1.1. The median overall survival (OS) was not reached and the median progression free survival (PFS) was 25.9 months. In terms of safety, PRRT was well tolerated. Review of the literature revealed consistent findings, supporting the efficacy and safety of PRRT in PPGL.
This study suggests that PRRT is a safe and effective therapeutic option for patients with PPGL. Our findings align with the existing literature, providing additional evidence to support the use of PRRT in this challenging patient population.
尽管在诊断和治疗方面取得了进展,但晚期嗜铬细胞瘤和副神经节瘤(PPGL)患者的治疗选择仍然有限。本研究旨在根据单机构经验评估肽受体放射性核素治疗(PRRT)在晚期 PPGL 患者中的安全性和疗效,并对文献进行全面综述。
对 2012 年 4 月至 2022 年 3 月期间在单机构接受 PRRT 的晚期嗜铬细胞瘤和副神经节瘤患者进行回顾性分析。评估了临床特征、治疗反应、不良反应和生存结局。还进行了系统的文献综述。
共纳入 15 例晚期 PPGL 患者,大多数患者同时患有转移性和功能性疾病。大多数患者接受了 4 次 177Lu-DOTATATE(73%)输注。每次输注的中位治疗性 177Lu-DOTATATE 放射性活度为 7.4GBq。仅 1 例患者除了接受 3 次 177Lu-DOTATATE 输注外,还额外接受了 1 次 90Y-DOTATATE(4.2GBq)输注。总体而言,PRRT 显示出有希望的疗效,根据 RECIST v1.1,疾病控制率为 63.6%。中位总生存期(OS)未达到,中位无进展生存期(PFS)为 25.9 个月。就安全性而言,PRRT 具有良好的耐受性。文献综述发现了一致的结果,支持 PRRT 在 PPGL 中的疗效和安全性。
本研究表明,PRRT 是 PPGL 患者的一种安全有效的治疗选择。我们的发现与现有文献一致,为在这一具有挑战性的患者群体中使用 PRRT 提供了额外的证据支持。