Literature DB >> 21190975

Clinical risk factors for malignancy and overall survival in patients with pheochromocytomas and sympathetic paragangliomas: primary tumor size and primary tumor location as prognostic indicators.

Montserrat Ayala-Ramirez1, Lei Feng, Marcella M Johnson, Shamim Ejaz, Mouhammed Amir Habra, Thereasa Rich, Naifa Busaidy, Gilbert J Cote, Nancy Perrier, Alexandria Phan, Shreyaskumar Patel, Steven Waguespack, Camilo Jimenez.   

Abstract

CONTEXT: Pheochromocytomas and sympathetic paragangliomas are rare neuroendocrine tumors for which no precise histological or molecular markers have been identified to differentiate benign from malignant tumors.
OBJECTIVE: The aim was to determine whether primary tumor location and size are associated with malignancy and decreased survival. DESIGN AND
SETTING: We performed a retrospective chart review of patients with either pheochromocytoma or sympathetic paraganglioma. PATIENTS: The study group comprised 371 patients. MAIN OUTCOME MEASURES: Overall survival and disease-specific survival were analyzed according to tumor size and location.
RESULTS: Sixty percent of patients with sympathetic paragangliomas and 25% of patients with pheochromocytomas had metastatic disease. Metastasis was more commonly associated with primary tumors located in the mediastinum (69%) and the infradiaphragmatic paraaortic area, including the organ of Zuckerkandl (66%). The primary tumor was larger in patients with metastases than in patients without metastatic disease (P < 0.0001). Patients with sympathetic paragangliomas had a shorter overall survival than patients with pheochromocytomas (P < 0.0001); increased tumor size was associated with shorter overall survival (P < 0.001). Patients with sympathetic paragangliomas were twice as likely to die of disease than patients with pheochromocytomas (hazard ratio = 1.93; 95% confidence interval = 1.20-3.12; P = 0.007). As per multivariate analysis, the location of the primary tumor was a stronger predictor of metastases than was the size of the primary tumor.
CONCLUSIONS: The size and location of the primary tumor were significant clinical risk factors for metastasis and decreased overall survival duration. These findings delineate the follow-up and treatment for these tumors.

Entities:  

Mesh:

Year:  2010        PMID: 21190975     DOI: 10.1210/jc.2010-1946

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


  134 in total

1.  Neuroendocrine cancer. Closing the GAPP on predicting metastases.

Authors:  Graeme Eisenhofer; Arthur S Tischler
Journal:  Nat Rev Endocrinol       Date:  2014-04-01       Impact factor: 43.330

2.  Images of pheochromocytoma in adrenal glands.

Authors:  Shaunagh McDermott; Colin J McCarthy; Michael A Blake
Journal:  Gland Surg       Date:  2015-08

3.  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

4.  SAGES guidelines for minimally invasive treatment of adrenal pathology.

Authors:  Dimitrios Stefanidis; Melanie Goldfarb; Kent W Kercher; William W Hope; William Richardson; Robert D Fanelli
Journal:  Surg Endosc       Date:  2013-09-10       Impact factor: 4.584

Review 5.  Treatment for Malignant Pheochromocytomas and Paragangliomas: 5 Years of Progress.

Authors:  Paola Jimenez; Claudio Tatsui; Aaron Jessop; Sonali Thosani; Camilo Jimenez
Journal:  Curr Oncol Rep       Date:  2017-10-28       Impact factor: 5.075

6.  Bone metastases and skeletal-related events in patients with malignant pheochromocytoma and sympathetic paraganglioma.

Authors:  Montserrat Ayala-Ramirez; J Lynn Palmer; Marie-Claude Hofmann; Maxine de la Cruz; Bryan S Moon; Steven G Waguespack; Mouhammed Amir Habra; Camilo Jimenez
Journal:  J Clin Endocrinol Metab       Date:  2013-02-22       Impact factor: 5.958

7.  Functional imaging for pheochromocytoma-paraganglioma: a step closer to understanding its place in clinical practice.

Authors:  Camilo Jimenez; Steven G Waguespack
Journal:  Endocrine       Date:  2015-06-26       Impact factor: 3.633

8.  SDHB large deletions are associated with absence of MIBG uptake in metastatic lesions of malignant paragangliomas.

Authors:  Janaina Petenuci; Gustavo F C Fagundes; Anna Flavia F Benedetti; Augusto G Guimaraes; Ana Caroline F Afonso; Flavia T Mota; Aurea Luiza F Magalhães; George B Coura-Filho; Maria Claudia N Zerbini; Sheila Siqueira; Fabio L M Montenegro; Victor Srougi; Fabio Y Tanno; Jose Luis Chambo; Marcela S S Ferrari; Joao Evangelista Bezerra Neto; Maria Adelaide A Pereira; Ana Claudia Latronico; Maria Candida B V Fragoso; Berenice B Mendonca; Ana O Hoff; Madson Q Almeida
Journal:  Endocrine       Date:  2021-01-09       Impact factor: 3.633

Review 9.  Pheochromocytoma: The First Metabolic Endocrine Cancer.

Authors:  Ivana Jochmanova; Karel Pacak
Journal:  Clin Cancer Res       Date:  2016-10-15       Impact factor: 12.531

10.  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

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