Safety and efficacy of peptide receptor radionuclide therapy in patients with advanced pheochromocytoma and paraganglioma: A single-institution experience and review of the literature

IF 3.3 4区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Charlene Yu Lin Tang, Wei Ming Chua, Hian Liang Huang, Winnie Wing-Chuen Lam, Lih Ming Loh, David Tai, Simon Yew Kuang Ong, Sean Xuexian Yan, Kelvin S. H. Loke, David Chee-Eng Ng, Wei Ying Tham
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Abstract

Introduction: 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. Methods: 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. Results: 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. Conclusion: 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.

Abstract Image

肽受体放射性核素治疗晚期嗜铬细胞瘤和副神经节瘤患者的安全性和有效性:单一机构经验和文献综述。
引言: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)患者的治疗选择有限。本研究旨在根据单一机构的经验,评估肽受体放射性核素治疗(PRRT)对晚期PPGL患者的安全性和有效性,并对文献进行全面综述。方法:对2012年4月至2022年3月在单一机构接受PRRT治疗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、不良事件和生存结果。还进行了系统的文献综述。结果:共纳入15例晚期PPGL患者,其中大多数同时患有转移性和功能性疾病。大多数患者接受了四次177Lu DOTATE输注(73%)。每次输注的177Lu DOTATATE放射性中位数为7.4 GBq。只有一名患者接受了一次90Y-DOTATE输液治疗(4.2 GBq)以及三次输注Lu-177 DOTATATE。总体而言,PRRT显示出一种有希望的疗效,RECIST v1.1的疾病控制率为63.6%。中位总生存期(OS)未达到,中位无进展生存期(PFS)为25.9 月。就安全性而言,PRRT耐受性良好。文献回顾显示了一致的结果,支持PRRT治疗PPGL的有效性和安全性。结论:本研究表明,PRRT是PPGL患者安全有效的治疗选择。我们的研究结果与现有文献一致,为支持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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Neuroendocrinology
Journal of Neuroendocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
6.20%
发文量
137
审稿时长
4-8 weeks
期刊介绍: Journal of Neuroendocrinology provides the principal international focus for the newest ideas in classical neuroendocrinology and its expanding interface with the regulation of behavioural, cognitive, developmental, degenerative and metabolic processes. Through the rapid publication of original manuscripts and provocative review articles, it provides essential reading for basic scientists and clinicians researching in this rapidly expanding field. In determining content, the primary considerations are excellence, relevance and novelty. While Journal of Neuroendocrinology reflects the broad scientific and clinical interests of the BSN membership, the editorial team, led by Professor Julian Mercer, ensures that the journal’s ethos, authorship, content and purpose are those expected of a leading international publication.
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