Literature DB >> 17102118

Courses of malignant pheochromocytoma: implications for therapy.

James C Sisson1, Barry L Shulkin, Nazanene H Esfandiari.   

Abstract

Survival of patients with metastatic pheochromocytoma that have exceeded 30 years without therapy to reduce tumors have been reported. We reviewed the records of 38 patients with malignant pheochromocytoma who had received 131I-metaiodiobenzylguanidine (131I-MIBG) treatments between 1981 and 1996 to evaluate longevity. Survival from diagnosis to last follow-up exceeded 5 years in 21 of 38 (55%) and >or=10 years in 50%. In 17 of 21, the interval from diagnosis to 131I-MIBG therapy was greater than 5 years. Survival following 131I-MIBG was >or=5 years in 12 of 17 and >or=10 years in 7 of 17 patients despite continued evidence of excessive circulating catecholamines. Objective responses to 131I-MIBG therapy were seen in about 30% and were usually of a few years, duration, but one individual exhibited marked reductions in volume and function of tumors that have persisted for 21 years. No feature, including a remission of >5 years following surgical excision, was found to predict prolonged survival. In summary, many patients with malignant pheochromocytoma will follow a course extending over many years. The role of 131I-MIBG therapy in longevity is uncertain, but this radiopharmaceutical reduces evidence of tumors in some patients. Criteria for selecting patients who will benefit from treatment remain to be determined.

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Year:  2006        PMID: 17102118     DOI: 10.1196/annals.1353.053

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  7 in total

Review 1.  Malignant pheochromocytomas and paragangliomas: a diagnostic challenge.

Authors:  Oliver Gimm; Catherine DeMicco; Aurel Perren; Francesco Giammarile; Martin K Walz; Laurent Brunaud
Journal:  Langenbecks Arch Surg       Date:  2011-11-29       Impact factor: 3.445

Review 2.  A clinical overview of pheochromocytomas/paragangliomas and carcinoid tumors.

Authors:  Ioannis Ilias; Karel Pacak
Journal:  Nucl Med Biol       Date:  2008-08       Impact factor: 2.408

Review 3.  Molecular and therapeutic advances in the diagnosis and management of malignant pheochromocytomas and paragangliomas.

Authors:  Aoife J Lowery; Siun Walsh; Enda W McDermott; Ruth S Prichard
Journal:  Oncologist       Date:  2013-04-10

4.  Systemic Radiopharmaceutical Therapy of Pheochromocytoma and Paraganglioma.

Authors:  Jorge A Carrasquillo; Clara C Chen; Abhishek Jha; Karel Pacak; Daniel A Pryma; Frank I Lin
Journal:  J Nucl Med       Date:  2021-09-01       Impact factor: 10.057

5.  LOCALLY INVASIVE PHEOCHROMOCYTOMA COMBINED WITH PRIMARY MALIGNANT ADRENAL LYMPHOMA.

Authors:  Omar H Oraibi; Laura I Wharry; Amy A Lynn; Foiqa Chaudhry; Juan C Jaume; John Y Jun
Journal:  AACE Clin Case Rep       Date:  2018-11-01

6.  Prognostic values of initial responses to low-dose (131)I-MIBG therapy in patients with malignant pheochromocytoma and paraganglioma.

Authors:  Hiroshi Wakabayashi; Junichi Taki; Anri Inaki; Ayane Nakamura; Daiki Kayano; Makoto Fukuoka; Shinro Matsuo; Kenichi Nakajima; Seigo Kinuya
Journal:  Ann Nucl Med       Date:  2013-07-18       Impact factor: 2.668

7.  A phase I clinical trial for [131I]meta-iodobenzylguanidine therapy in patients with refractory pheochromocytoma and paraganglioma.

Authors:  Hiroshi Wakabayashi; Anri Inaki; Kenichi Yoshimura; Toshinori Murayama; Yasuhito Imai; Tetsuya Higuchi; Megumi Jinguji; Tohru Shiga; Seigo Kinuya
Journal:  Sci Rep       Date:  2019-05-20       Impact factor: 4.379

  7 in total

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