Predictors of malignancy in patients with pheochromocytomas/paragangliomas: Asian Indian experience

Background and aims Malignant transformation of pheochromocytomas/paragangliomas (PCC/PGL) is a rare occurrence, and predictive factors for the same are not well understood. This study aims to identify the predictors of malignancy in patients with PCC/PGL. Materials and methods We performed a retrospective analysis of 142 patients with either PCC or PGL registered at our institute between 2000 and 2015. Records were evaluated for clinical parameters like age, gender, familial/syndromic presentation, symptomatic presentation, biochemistry, size, number and location of tumours and presence of metastases and mode of its diagnosis. Results Twenty patients were found to have metastases; 13 had metastases at diagnosis and seven during follow-up. Metastases were detected by radiology (CT-neck to pelvis) in 11/20 patients (5/13 synchronous and 6/7 metachronous), 131I-metaiodobenzylguanidine in five (2/12 synchronous and 3/6 metachronous) patients and 18F-flurodeoxyglucose PET/CT in 15 (12/12 synchronous and 3/3 metachronous) patients. Malignant tumours were significantly larger than benign tumours (8.3 ± 4.1 cm, range: 3–22 cm vs 5.7 ± 2.3 cm, range: 2–14 cm, P = 0.0001) and less frequently metanephrine secreting. On linear regression analysis, tumour size and lack of metanephrine secretion were the independent predictors of malignancy. Conclusions Patients with primary tumour size >5.7 cm and lack of metanephrine secretory status should be evaluated for possible malignancy not only at diagnosis but also in the postoperative period. As compared to CT and 131I-MIBG scan, 18F-flurodeoxyglucose PET/CT analyses are better (sensitivity: 100%) for the diagnosis of metastases in our study.

[1]  O. Dekkers,et al.  European Society of Endocrinology Clinical Practice Guideline for long-term follow-up of patients operated on for a phaeochromocytoma or a paraganglioma. , 2016, European journal of endocrinology.

[2]  Jungsuk An,et al.  Phenylethanolamine N-methyltransferase downregulation is associated with malignant pheochromocytoma/paraganglioma , 2016, Oncotarget.

[3]  S. Khare,et al.  Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma. , 2016, European journal of endocrinology.

[4]  K. Pacak,et al.  15 YEARS OF PARAGANGLIOMA: Imaging and imaging-based treatment of pheochromocytoma and paraganglioma. , 2015, Endocrine-related cancer.

[5]  S. Fanti,et al.  Diagnostic and prognostic value of 18F-FDG PET/CT in comparison with morphological imaging in primary adrenal gland malignancies - a multicenter experience. , 2015, Hellenic journal of nuclear medicine.

[6]  Elise M. Blanchet,et al.  Superiority of [68Ga]-DOTATATE PET/CT to Other Functional Imaging Modalities in the Localization of SDHB-Associated Metastatic Pheochromocytoma and Paraganglioma , 2015, Clinical Cancer Research.

[7]  E. Baudin,et al.  Therapy of endocrine disease: treatment of malignant pheochromocytoma and paraganglioma. , 2014, European journal of endocrinology.

[8]  T. Fojo,et al.  The size of the primary tumor and age at initial diagnosis are independent predictors of the metastatic behavior and survival of patients with SDHB-related pheochromocytoma and paraganglioma: a retrospective cohort study , 2014, BMC Cancer.

[9]  W. Young,et al.  Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. , 2014, The Journal of clinical endocrinology and metabolism.

[10]  P. Castaldi,et al.  Comparison of metaiodobenzylguanidine scintigraphy with positron emission tomography in the diagnostic work-up of pheochromocytoma and paraganglioma: a systematic review. , 2013, The quarterly journal of nuclear medicine and molecular imaging : official publication of the Italian Association of Nuclear Medicine (AIMN) [and] the International Association of Radiopharmacology (IAR), [and] Section of the Society of....

[11]  S. Bornstein,et al.  Plasma methoxytyramine: a novel biomarker of metastatic pheochromocytoma and paraganglioma in relation to established risk factors of tumour size, location and SDHB mutation status. , 2012, European journal of cancer.

[12]  B. Paghera,et al.  Role of 18F-FDG PET/CT, 123I-MIBG SPECT, and CT in Restaging Patients Affected by Malignant Pheochromocytoma , 2011, Nuclear medicine and molecular imaging.

[13]  F. Feng,et al.  Predictive factors for malignant pheochromocytoma: analysis of 136 patients. , 2011, The Journal of urology.

[14]  Lei Feng,et al.  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. , 2011, The Journal of clinical endocrinology and metabolism.

[15]  Choung-Soo Kim,et al.  Predictive Characteristics of Malignant Pheochromocytoma , 2009, Korean journal of urology.

[16]  M. Fraenkel,et al.  Malignant pheochromocytoma: predictive factors of malignancy and clinical course in 16 patients at a single tertiary medical center , 2011, Endocrine.

[17]  G. Arnaldi,et al.  Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas. , 2009, The Journal of clinical endocrinology and metabolism.

[18]  A. González-Neira,et al.  Genetics of pheochromocytoma and paraganglioma in Spanish patients. , 2009, The Journal of clinical endocrinology and metabolism.

[19]  J. Carrasquillo,et al.  Comparison of 18F-fluoro-L-DOPA, 18F-fluoro-deoxyglucose, and 18F-fluorodopamine PET and 123I-MIBG scintigraphy in the localization of pheochromocytoma and paraganglioma. , 2009, The Journal of clinical endocrinology and metabolism.

[20]  J. Carrasquillo,et al.  I-MIBG Scintigraphy in the Localization of Pheochromocytoma and Paraganglioma , 2017 .

[21]  A. Tischler Pheochromocytoma: Time to Stamp Out “Malignancy”? , 2008, Endocrine pathology.

[22]  Laura H. Tang,et al.  Prognostic indicators of malignancy in adrenal pheochromocytomas: clinical, histopathologic, and cell cycle/apoptosis gene expression analysis. , 2008, Surgery.

[23]  E. Baudin,et al.  Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas. , 2007, The Journal of clinical endocrinology and metabolism.

[24]  A. Grossman,et al.  The diagnosis and management of malignant phaeochromocytoma and paraganglioma. , 2007, Endocrine-related cancer.

[25]  S. Richard,et al.  Genetic testing in pheochromocytoma or functional paraganglioma. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[26]  N. Kimura,et al.  Histological grading of adrenal and extra-adrenal pheochromocytomas and relationship to prognosis: A clinicopathological analysis of 116 adrenal pheochromocytomas and 30 extra-adrenal sympathetic paragangliomas including 38 malignant tumors , 2005, Endocrine pathology.

[27]  Q. Duh,et al.  Should pheochromocytoma size influence surgical approach? A comparison of 90 malignant and 60 benign pheochromocytomas. , 2004, Surgery.

[28]  David I. Smith,et al.  Malignant pheochromocytoma: current status and initiatives for future progress. , 2004, Endocrine-related cancer.

[29]  Jie Gao,et al.  [Distinction between benign and malignant pheochromocytomas]. , 2004, Zhonghua bing li xue za zhi = Chinese journal of pathology.

[30]  R. DeLellis Pathology and genetics of tumours of endocrine organs , 2004 .

[31]  L. Thompson Pheochromocytoma of the Adrenal Gland Scaled Score (PASS) to Separate Benign From Malignant Neoplasms: A Clinicopathologic and Immunophenotypic Study of 100 Cases , 2002, The American journal of surgical pathology.

[32]  D. Hauri,et al.  Pheochromocytomas: can malignant potential be predicted? , 1999, Urology.