Literature DB >> 19470630

Survival of patients with metastatic malignant pheochromocytoma and efficacy of combined cyclophosphamide, vincristine, and dacarbazine chemotherapy.

Kaoru Nomura1, Hironari Kimura, Satoru Shimizu, Hitomi Kodama, Takahiro Okamoto, Takao Obara, Kazue Takano.   

Abstract

CONTEXT: About 10% of pheochromocytomas are malignant. Exact survival has not been reported, nor has an analysis of the efficacy of chemotherapy on survival time.
OBJECTIVE: The aim of this study was to analyze the survival curves and survival times of patients with malignant pheochromocytoma and to determine the efficacy of chemotherapy on prolongation of life.
DESIGN: An inception cohort and Kaplan-Meier survival analysis was conducted. PATIENTS AND OUTCOME MEASURES: Thirty-two patients with metastasized malignant pheochromocytoma were analyzed for survival. Twenty-five patients had undergone excision of their primary tumors. Survival curves were compared among the 16 patients in this group treated with combined chemotherapy using cyclophosphamide, vincristine and dacarbazine (CVD) and the nine patients not treated with chemotherapy.
RESULTS: The survival curve of the 32 patients declined continuously and linearly to at least 20 yr after the diagnosis of pheochromocytoma. The 50% survival rate was estimated to be 14.7 yr. In the 25 patients whose primary tumor was excised, patients who already had metastases at the time of pheochromocytoma diagnosis had better survival than those whose metastases were found later. The survival rate after diagnosis of metastasis was worse in the CVD group than in controls. When the effects of CVD were examined after stratifying several factors, female gender and adrenal origin of tumor were found to be negative prognostic factors for CVD chemotherapy.
CONCLUSION: The present study revealed a long survival time. CVD chemotherapy was not shown to extend survival, especially for women and patients with adrenal gland-derived primary tumors.

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Year:  2009        PMID: 19470630     DOI: 10.1210/jc.2008-2697

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  23 in total

1.  Extraadrenal pheochromocytoma and vagal paraganglioma.

Authors:  Andrew W Jennings; John T Preskitt; Raphaelle D Vallera
Journal:  Proc (Bayl Univ Med Cent)       Date:  2012-04

2.  Clinical benefits of systemic chemotherapy for patients with metastatic pheochromocytomas or sympathetic extra-adrenal paragangliomas: insights from the largest single-institutional experience.

Authors:  Montserrat Ayala-Ramirez; Lei Feng; Mouhammed A Habra; Thereasa Rich; Paxton V Dickson; Nancy Perrier; Alexandria Phan; Steven Waguespack; Shreyaskumar Patel; Camilo Jimenez
Journal:  Cancer       Date:  2011-10-17       Impact factor: 6.860

Review 3.  Pheochromocytomas and paragangliomas: assessment of malignant potential.

Authors:  Tim I M Korevaar; Ashley B Grossman
Journal:  Endocrine       Date:  2011-10-25       Impact factor: 3.633

Review 4.  Metastatic paraganglioma.

Authors:  Stephanie M J Fliedner; Hendrik Lehnert; Karel Pacak
Journal:  Semin Oncol       Date:  2010-12       Impact factor: 4.929

5.  Paraganglioma: not just an extra-adrenal pheochromocytoma.

Authors:  Amanda M Laird; Paul G Gauger; Gerard M Doherty; Barbra S Miller
Journal:  Langenbecks Arch Surg       Date:  2011-11-17       Impact factor: 3.445

Review 6.  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

Review 7.  Outcomes of patients with metastatic phaeochromocytoma and paraganglioma: A systematic review and meta-analysis.

Authors:  Oksana Hamidi; William F Young; Lucinda Gruber; John Smestad; Qi Yan; Oscar J Ponce; Larry Prokop; Mohammad Hassan Murad; Irina Bancos
Journal:  Clin Endocrinol (Oxf)       Date:  2017-08-17       Impact factor: 3.478

8.  Combination chemotherapy with cyclophosphamide, vincristine, and dacarbazine in patients with malignant pheochromocytoma and paraganglioma.

Authors:  Akiyo Tanabe; Mitsuhide Naruse; Kaoru Nomura; Mika Tsuiki; Aya Tsumagari; Atsuhiro Ichihara
Journal:  Horm Cancer       Date:  2013-01-30       Impact factor: 3.869

9.  Targeting NAD+/PARP DNA Repair Pathway as a Novel Therapeutic Approach to SDHB-Mutated Cluster I Pheochromocytoma and Paraganglioma.

Authors:  Ying Pang; Yanxin Lu; Veronika Caisova; Yang Liu; Petra Bullova; Thanh-Truc Huynh; Yiqiang Zhou; Di Yu; Zdenek Frysak; Igor Hartmann; David Taïeb; Karel Pacak; Chunzhang Yang
Journal:  Clin Cancer Res       Date:  2018-04-10       Impact factor: 12.531

Review 10.  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
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