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

Author:

Tang Charlene Yu Lin12ORCID,Chua Wei Ming13,Huang Hian Liang12,Lam Winnie Wing‐Chuen12,Loh Lih Ming4,Tai David25,Ong Simon Yew Kuang25,Yan Sean Xuexian126,Loke Kelvin S. H.12,Ng David Chee‐Eng12,Tham Wei Ying12

Affiliation:

1. Department of Nuclear Medicine and Molecular Imaging Singapore General Hospital Singapore Singapore

2. Duke‐NUS Medical School Singapore Singapore

3. Department of Neuroradiology Singapore General Hospital Singapore Singapore

4. Department of Endocrinology Singapore General Hospital Singapore Singapore

5. Division of Medical Oncology, National Cancer Centre Singapore Singapore

6. Department of Radiology University of Texas Southwestern Medical Center Dallas Texas United States

Abstract

AbstractIntroduction: 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.

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Endocrine and Autonomic Systems,Endocrinology,Endocrinology, Diabetes and Metabolism

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