Surveillance of succinate dehydrogenase gene mutation carriers: Insights from a nationwide cohort

• Type: Article in International Scientific Journal
• Date: 2020

Authors

R Martins (Author) FMUP; Cunha, N (Author) Other; Simoes, H (Author) Other; Matos, MJ (Author) Other; Silva, J (Author) Other; Torres, I (Author) Other; Rodrigues, F (Author) Other; Leite, V (Author) Other; Manuel R Teixeira (Author) ICBAS; Bugalho, MJ (Author) Other

Journal

Title: Clinical Endocrinology

Vol. 92

Pages: 545-553

ISSN: 0300-0664

Publisher: Wiley-Blackwell

Indexing

ISI Web of Knowledge - 9 Citations

Scopus - 8 Citations

Other information

Authenticus ID: P-00S-M28

DOI: 10.1111/cen.14184

Abstract (EN): Objective Mutations in the genes coding for succinate dehydrogenase (SDHx) are the most frequent germline alterations in pheochromocytomas and paragangliomas. Evidence for the advantages associated with presymptomatic screening for SDHx mutation carriers is scarce. This study describes a nationwide cohort of these mutation carriers and aims to compare patients with clinical manifestations of the disease and those diagnosed through genetic screening. DESIGN: Cross-sectional study. Patients SDHx mutation carriers (n = 118) followed through the Portuguese Oncology referral centres: 41 probands and 77 nonprobands. Measurements All participants were subjected to biochemical and body imaging examinations for a complete assessment of the extent and spread of disease. Clinical data obtained this way were further analysed. Results The mean age of this cohort was 44.5 +/- 17.4 years, and more than half carried the same founder SDHB mutation. About 50.8% of the mutation carriers developed pheochromocytomas or paragangliomas. Compared to patients diagnosed through genetic screening, those diagnosed clinically were characterized by larger tumours (P < .001), more frequent metastases (P = .024), were more frequently subjected to surgery (P = .011) and radiotherapy (P = .013), and had worse outcomes, such as macroscopic positive margins (P = .034). Persistent and/or unresectable disease and disease-related mortality were also more frequent in symptomatic patients compared to those diagnosed through genetic screening (P = .014). Conclusions In this nationwide cohort study, a large proportion of mutation carriers were found to develop SDHx-related neoplasia. Genetic testing and subsequent follow-up resulted in the diagnosis of smaller and nonmetastatic tumours, fewer treatment procedures, fewer complications and greater number of disease-free patients.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 9