Approach to the Patient With Metastatic Pheochromocytoma and Paraganglioma

Phe ochromocytomas and paragangliomas (PPGLs) are rare neural crest-derived tumors with malignant potential and a highly variable natural history, where some patients achieve a cure through surgical resection, while others experience an aggressive and protracted disease course characterized by recurrence and metastasis. While currently no definitive curative treatment exists for metastatic PPGLs, ongoing trials and advances in biology of the disease present a beacon of hope. We present a case that illustrates a 15-year treatment journey, illustrating the complexity of metastatic PPGL treatment with different modalities, each with distinct efficacy and toxicity profiles. The choice of treatment is often an art, as much as it is based on evidence, as the clinician must balance among several factors, including tumor-related (pace of progression, tumor burden) and patient-related (functional status, symptoms, general health) ones. Through a stepwise approach, this discussion aims to provide insights into the evolving landscape of metastatic PPGL management.

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Institutions

Publication Details

Journal
The Journal of Clinical Endocrinology & Metabolism
Published
2025-05-01
DOI
https://doi.org/10.1210/clinem/dgaf259
Citations
13
Primary Topic
Adrenal and Paraganglionic Tumors
Type
article
Field-Weighted Citation Impact
26.08
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article

Approach to the Patient With Metastatic Pheochromocytoma and Paraganglioma

David Taïeb, Jaydira Del Rivero, Katharina Wang, Roderick John Clifton-Bligh et al.
13 citations
The Journal of Clinical Endocrinology & Metabolism
Adrenal and Paraganglionic Tumors
26.08
article

Approach to the Patient With Metastatic Pheochromocytoma and Paraganglioma

David Taïeb, Jaydira Del Rivero, Katharina Wang, Roderick John Clifton-Bligh, Hussam Alkaissi, Karel Pacák, Frank I. Lin
article en
13 citations

Abstract

Phe ochromocytomas and paragangliomas (PPGLs) are rare neural crest-derived tumors with malignant potential and a highly variable natural history, where some patients achieve a cure through surgical resection, while others experience an aggressive and protracted disease course characterized by recurrence and metastasis. While currently no definitive curative treatment exists for metastatic PPGLs, ongoing trials and advances in biology of the disease present a beacon of hope. We present a case that illustrates a 15-year treatment journey, illustrating the complexity of metastatic PPGL treatment with different modalities, each with distinct efficacy and toxicity profiles. The choice of treatment is often an art, as much as it is based on evidence, as the clinician must balance among several factors, including tumor-related (pace of progression, tumor burden) and patient-related (functional status, symptoms, general health) ones. Through a stepwise approach, this discussion aims to provide insights into the evolving landscape of metastatic PPGL management.

The Journal of Clinical Endocrinology & MetabolismVol. 110(10)
The University of Sydney (AU), National Institutes of Health (US), Aix-Marseille Université (FR), Royal North Shore Hospital (AU), Endocrine Society (US), National Institute of Diabetes and Digestive and Kidney Diseases (US), National Cancer Institute (UA), Institut de Neurosciences de la Timone (FR), National Cancer Institute (US), Eunice Kennedy Shriver National Institute of Child Health and Human Development (US), Center for Cancer Research (US), Hôpital de la Timone (FR), Ludwig-Maximilians-Universität München (DE)
Good health and well-being
Openalex Percentile: Top 0%
Adrenal and Paraganglionic Tumors
26.08
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