Literature DB >> 27857127

Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas.

Rodrigo A Toledo1,2, Nelly Burnichon3,4, Alberto Cascon5, Diana E Benn6, Jean-Pierre Bayley7, Jenny Welander8, Carli M Tops9, Helen Firth10, Trish Dwight6, Tonino Ercolino11, Massimo Mannelli11, Giuseppe Opocher12, Roderick Clifton-Bligh6, Oliver Gimm13, Eamonn R Maher10, Mercedes Robledo5, Anne-Paule Gimenez-Roqueplo3,4, Patricia L M Dahia1.   

Abstract

Phaeochromocytomas and paragangliomas (PPGLs) are neural-crest-derived tumours of the sympathetic or parasympathetic nervous system that are often inherited and are genetically heterogeneous. Genetic testing is recommended for patients with these tumours and for family members of patients with hereditary forms of PPGLs. Due to the large number of susceptibility genes implicated in the diagnosis of inherited PPGLs, next-generation sequencing (NGS) technology is ideally suited for carrying out genetic screening of these individuals. This Consensus Statement, formulated by a study group comprised of experts in the field, proposes specific recommendations for the use of diagnostic NGS in hereditary PPGLs. In brief, the study group recommends target gene panels for screening of germ line DNA, technical adaptations to address different modes of disease transmission, orthogonal validation of NGS findings, standardized classification of variant pathogenicity and uniform reporting of the findings. The use of supplementary assays, to aid in the interpretation of the results, and sequencing of tumour DNA, for identification of somatic mutations, is encouraged. In addition, the study group launches an initiative to develop a gene-centric curated database of PPGL variants, with annual re-evaluation of variants of unknown significance by an expert group for purposes of reclassification and clinical guidance.

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Year:  2016        PMID: 27857127     DOI: 10.1038/nrendo.2016.185

Source DB:  PubMed          Journal:  Nat Rev Endocrinol        ISSN: 1759-5029            Impact factor:   43.330


  57 in total

1.  Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas.

Authors:  Laura Remacha; David Pirman; Christopher E Mahoney; Javier Coloma; Bruna Calsina; Maria Currás-Freixes; Rocío Letón; Rafael Torres-Pérez; Susan Richter; Guillermo Pita; Belén Herráez; Giovanni Cianchetta; Emiliano Honrado; Lorena Maestre; Miguel Urioste; Javier Aller; Óscar García-Uriarte; María Ángeles Gálvez; Raúl M Luque; Marcos Lahera; Cristina Moreno-Rengel; Graeme Eisenhofer; Cristina Montero-Conde; Cristina Rodríguez-Antona; Óscar Llorca; Gromoslaw A Smolen; Mercedes Robledo; Alberto Cascón
Journal:  Am J Hum Genet       Date:  2019-03-28       Impact factor: 11.025

2.  Tumor multifocality with vagus nerve involvement as a phenotypic marker of SDHD mutation in patients with head and neck paragangliomas: A 18 F-FDOPA PET/CT study.

Authors:  Vincent Amodru; Pauline Romanet; Ugo Scemama; Marion Montava; Nicolas Fakhry; Frédéric Sebag; Frédéric Castinetti; Jean-Pierre Lavieille; Anderson Loundou; Arthur Varoquaux; Anne Barlier; Karel Pacak; David Taïeb
Journal:  Head Neck       Date:  2018-12-24       Impact factor: 3.147

Review 3.  Fit-for-Purpose Immunohistochemical Biomarkers.

Authors:  Emina Emilia Torlakovic
Journal:  Endocr Pathol       Date:  2018-06       Impact factor: 3.943

Review 4.  What Have We Learned from Molecular Biology of Paragangliomas and Pheochromocytomas?

Authors:  Thomas G Papathomas; Diederik P D Suurd; Alfred K Lam; Ronald R de Krijger; Karel Pacak; Arthur S Tischler; Menno R Vriens
Journal:  Endocr Pathol       Date:  2021-01-12       Impact factor: 3.943

Review 5.  PRECISION MEDICINE: AN UPDATE ON GENOTYPE/BIOCHEMICAL PHENOTYPE RELATIONSHIPS IN PHEOCHROMOCYTOMA/PARAGANGLIOMA PATIENTS.

Authors:  Garima Gupta; Karel Pacak
Journal:  Endocr Pract       Date:  2017-03-23       Impact factor: 3.443

6.  Routine genetic screening with a multi-gene panel in patients with pheochromocytomas.

Authors:  Emilia Sbardella; Treena Cranston; Andrea M Isidori; Brian Shine; Aparna Pal; Bahram Jafar-Mohammadi; Greg Sadler; Radu Mihai; Ashley B Grossman
Journal:  Endocrine       Date:  2017-05-05       Impact factor: 3.633

Review 7.  Paragangliomas of the Head and Neck: An Overview from Diagnosis to Genetics.

Authors:  Michelle D Williams
Journal:  Head Neck Pathol       Date:  2017-03-20

Review 8.  Primary cardiac tumors associated with genetic syndromes: a comprehensive review.

Authors:  Elizabeth Lee; Maryam Ghadimi Mahani; Jimmy C Lu; Adam L Dorfman; Ashok Srinivasan; Prachi P Agarwal
Journal:  Pediatr Radiol       Date:  2017-12-06

9.  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 10.  Genetic Testing in Endocrinology.

Authors:  Sunita Mc De Sousa; Tristan Se Hardy; Hamish S Scott; David J Torpy
Journal:  Clin Biochem Rev       Date:  2018-02
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