Literature DB >> 28685225

Phase II trial of pazopanib in advanced/progressive malignant pheochromocytoma and paraganglioma.

Sina Jasim1, Vera J Suman2, Camilo Jimenez3, Pamela Harris4, Kostandinos Sideras5,6, Jill K Burton5, Francis Paul Worden7, Richard J Auchus8, Keith C Bible9.   

Abstract

INTRODUCTION: Pheochromocytomas and paragangliomas (Pheo/PGL) are rare, vascular, sometimes malignant endocrine tumors. Case reports indicate the activity of vascular endothelium growth factor receptor-targeted kinase inhibitors in these cancers.
OBJECTIVES: To assess the antitumor activity and tolerability of pazopanib in progressive malignant Pheo/PGL. PATIENTS AND METHODS: This multicenter Phase II trial (MC107C) enrolled individuals  ≥18 years old with disease progression ≤ 6 months prior to registration, Eastern Cooperative Oncology Group PS 0-2, and measurable disease (response evaluation criteria in solid tumors 1.0). Pazopanib was administered in 28-day cycles, with the regimen ultimately being as follows: cycle 1: 400 mg daily on days 1-14, cycle 2: 800 mg daily on days 1-14, and then cycle 2 + : 800 mg daily on all days.
RESULTS: The study was halted due to poor accrual. Seven patients were enrolled (05/2011-11/2014). One patient withdrew consent prior to treatment, leaving six evaluable patients. Treatment was discontinued, due to the following reasons: disease progression (4); withdrawal (1); and grade 4 (Takotsubo) cardiomyopathy (1). The median number of cycles administered was 4 (range: 2-29, total: 49). Four patients had >1 dose reduction due to the following reasons: fatigue (1), abnormal liver tests (2), hypertension and (Takotsubo) cardiomyopathy (1), and headaches (1). Common severe (Common Terminology Criteria for Adverse Events v3.0 grades 3-5) toxicities were as follows: hypertension (3/6), (Takotsubo) cardiomyopathy (2/6), diarrhea (1/6), fatigue (1/6), headache (1/6), and hematuria (1/6). One confirmed partial response was observed in PGL (17%, duration 2.4 years); median progression-free survival and overall survival were 6.5 and 14.8 months, respectively.
CONCLUSION: Pazopanib has activity in Pheo/PGL requiring more study; optimal alpha- and beta-blockade are imperative pre-therapy in patients with secretory tumors, as risk of hypertension and cardiomyopathy are potentially life threatening.

Entities:  

Keywords:  Metastatic; Paraganglioma; Pazopanib; Takotsubo cardiomyopathy

Mesh:

Substances:

Year:  2017        PMID: 28685225     DOI: 10.1007/s12020-017-1359-5

Source DB:  PubMed          Journal:  Endocrine        ISSN: 1355-008X            Impact factor:   3.925


  9 in total

1.  Efficacy of pazopanib in progressive, radioiodine-refractory, metastatic differentiated thyroid cancers: results of a phase 2 consortium study.

Authors:  Keith C Bible; Vera J Suman; Julian R Molina; Robert C Smallridge; William J Maples; Michael E Menefee; Joseph Rubin; Kostandinos Sideras; John C Morris; Bryan McIver; Jill K Burton; Kevin P Webster; Carolyn Bieber; Anne M Traynor; Patrick J Flynn; Boon Cher Goh; Hui Tang; Susan Percy Ivy; Charles Erlichman
Journal:  Lancet Oncol       Date:  2010-09-17       Impact factor: 41.316

2.  Tumor angiogenesis in pheochromocytomas and paragangliomas.

Authors:  Q Liu; G Djuricin; E D Staren; P Gattuso; V E Gould; J Shen; T Saclarides; D B Rubin; R A Prinz
Journal:  Surgery       Date:  1996-12       Impact factor: 3.982

3.  Treatment with sunitinib for patients with progressive metastatic pheochromocytomas and sympathetic paragangliomas.

Authors:  Montserrat Ayala-Ramirez; Cecile N Chougnet; Mouhammed Amir Habra; J Lynn Palmer; Sophie Leboulleux; Maria E Cabanillas; Caroline Caramella; Pete Anderson; Abir Al Ghuzlan; Steven G Waguespack; Desirée Deandreis; Eric Baudin; Camilo Jimenez
Journal:  J Clin Endocrinol Metab       Date:  2012-09-10       Impact factor: 5.958

4.  VEGF in 105 pheochromocytomas: enhanced expression correlates with malignant outcome.

Authors:  Kaisa Salmenkivi; Päivi Heikkilä; Jianqi Liu; Caj Haglund; Johanna Arola
Journal:  APMIS       Date:  2003-04       Impact factor: 3.205

5.  Angiogenesis and vascular architecture in pheochromocytomas: distinctive traits in malignant tumors.

Authors:  Judith Favier; Pierre-François Plouin; Pierre Corvol; Jean-Marie Gasc
Journal:  Am J Pathol       Date:  2002-10       Impact factor: 4.307

6.  VEGF-mediated angiogenesis of human pheochromocytomas is associated to malignancy and inhibited by anti-VEGF antibodies in experimental tumors.

Authors:  Andreas Zielke; Martin Middeke; Sebastian Hoffmann; Mario Colombo-Benkmann; Peter Barth; Iyad Hassan; Annette Wunderlich; Lorenz C Hofbauer; Quan-Yang Duh
Journal:  Surgery       Date:  2002-12       Impact factor: 3.982

7.  Use of the tyrosine kinase inhibitor sunitinib in a patient with von Hippel-Lindau disease: targeting angiogenic factors in pheochromocytoma and other von Hippel-Lindau disease-related tumors.

Authors:  Camilo Jimenez; Maria E Cabanillas; Libero Santarpia; Eric Jonasch; Karen L Kyle; Elizabeth A Lano; Surena F Matin; Rodolfo F Nunez; Nancy D Perrier; Alexandria Phan; Thereasa A Rich; Beejal Shah; Michelle D Williams; Steven G Waguespack
Journal:  J Clin Endocrinol Metab       Date:  2008-11-18       Impact factor: 5.958

Review 8.  Malignant pheochromocytoma: current status and initiatives for future progress.

Authors:  Graeme Eisenhofer; Stefan R Bornstein; Frederieke M Brouwers; Nai-Kong V Cheung; Patricia L Dahia; Ronald R de Krijger; Thomas J Giordano; Lloyd A Greene; David S Goldstein; Hendrik Lehnert; William M Manger; John M Maris; Hartmut P H Neumann; Karel Pacak; Barry L Shulkin; David I Smith; Arthur S Tischler; William F Young
Journal:  Endocr Relat Cancer       Date:  2004-09       Impact factor: 5.678

9.  Rationale and evidence for sunitinib in the treatment of malignant paraganglioma/pheochromocytoma.

Authors:  Anthony M Joshua; Shereen Ezzat; Sylvia L Asa; Andrew Evans; Reuben Broom; Marc Freeman; Jennifer J Knox
Journal:  J Clin Endocrinol Metab       Date:  2008-11-11       Impact factor: 5.958

  9 in total
  19 in total

Review 1.  Metastatic Phaeochromocytoma: Spinning Towards More Promising Treatment Options.

Authors:  Svenja Nölting; Ashley Grossman; Karel Pacak
Journal:  Exp Clin Endocrinol Diabetes       Date:  2018-09-20       Impact factor: 2.949

Review 2.  New Perspectives on Pheochromocytoma and Paraganglioma: Toward a Molecular Classification.

Authors:  Joakim Crona; David Taïeb; Karel Pacak
Journal:  Endocr Rev       Date:  2017-12-01       Impact factor: 19.871

3.  HEREDITARY ENDOCRINE TUMOURS: CURRENT STATE-OF-THE-ART AND RESEARCH OPPORTUNITIES: Metastatic pheochromocytomas and paragangliomas: proceedings of the MEN2019 workshop.

Authors:  Patricia L M Dahia; Roderick Clifton-Bligh; Anne-Paule Gimenez-Roqueplo; Mercedes Robledo; Camilo Jimenez
Journal:  Endocr Relat Cancer       Date:  2020-08       Impact factor: 5.678

Review 4.  Recent advances in the management of pheochromocytoma and paraganglioma.

Authors:  Akiyo Tanabe; Mitsuhide Naruse
Journal:  Hypertens Res       Date:  2020-08-11       Impact factor: 3.872

5.  The use of telemedicine in the preoperative management of pheochromocytoma saves resources.

Authors:  Martin Joseph Heslin; Joe-Spencer Liles; Paulina Moctezuma-Velázquez
Journal:  Mhealth       Date:  2019-08-20

6.  High-specific-activity 131iodine-metaiodobenzylguanidine for therapy of unresectable pheochromocytoma and paraganglioma.

Authors:  Joseph S Dillon; David Bushnell; Douglas E Laux
Journal:  Future Oncol       Date:  2021-01-28       Impact factor: 3.404

Review 7.  New Directions in Treatment of Metastatic or Advanced Pheochromocytomas and Sympathetic Paragangliomas: an American, Contemporary, Pragmatic Approach.

Authors:  Camilo Jimenez; Guofan Xu; Jeena Varghese; Paul H Graham; Matthew T Campbell; Yang Lu
Journal:  Curr Oncol Rep       Date:  2022-01-21       Impact factor: 5.075

Review 8.  Advances in adrenal tumors 2018.

Authors:  J Crona; F Beuschlein; K Pacak; B Skogseid
Journal:  Endocr Relat Cancer       Date:  2018-07       Impact factor: 5.678

Review 9.  Treatment for Patients With Malignant Pheochromocytomas and Paragangliomas: A Perspective From the Hallmarks of Cancer.

Authors:  Camilo Jimenez
Journal:  Front Endocrinol (Lausanne)       Date:  2018-05-28       Impact factor: 5.555

Review 10.  Recent advances in the management of malignant pheochromocytoma and paraganglioma: focus on tyrosine kinase and hypoxia-inducible factor inhibitors.

Authors:  Rodrigo Toledo; Camilo Jimenez
Journal:  F1000Res       Date:  2018-07-30
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