Literature DB >> 31194233

Characterization of Malignant Head and Neck Paragangliomas at a Single Institution Across Multiple Decades.

Hilary C McCrary1, Eric Babajanian1, Matias Calquin2, Patrick Carpenter1, Geoffrey Casazza1, Anne Naumer3, Samantha Greenberg3, Wendy Kohlmann3, Richard Cannon1, Marcus M Monroe1, Jason P Hunt1, Luke Buchmann1.   

Abstract

Importance: Malignant head and neck paragangliomas (HNPGLs) are rare entities, and there are limited data regarding optimal treatment recommendations to improve clinical outcomes. Objective: To classify succinate dehydrogenase (SDH) germline mutations associated with malignant HNPGLs, evaluate time from diagnosis to identification of malignant tumor, describe locations of metastases and the functional status of malignant HNPGLs, and determine the role of selective neck dissection at the time of initial surgical resection. Design, Setting, and Participants: A retrospective cohort study was completed of patients diagnosed with paragangliomas on various sites on the body at an academic tertiary cancer hospital between the years 1963 and 2018. A subanalysis of HNPGLs was also completed. Data regarding diagnosis, gene and mutation, tumor characteristics and location, and treatments used were reviewed between February 2017 and March 2018. Main Outcomes and Measures: Mutations of SDH genes associated with benign and malignant HNPGLs, treatments used, time to the discovery of malignancy, and location of metastasis.
Results: Of the 70 patients included in the study, 40 (57%) were male, and the mean (SD) age was 47 (21.1) years. Of patients with tumors isolated to the head and neck, 38 (54%) had benign HNPGLs, which were associated with mutations in the genes SDH subunit B (SDHB) (n = 18; 47%), SDH subunit C (n = 2; 5%), and SDH subunit D (n = 18; 47%). Among those with malignant HNPGLs, all but 1 patient had mutations in SDHB (n = 5; 83%); 1 patient had no mutation associated with their disease. The average age at diagnosis for malignant HNPGLs was 35 years, while benign tumors were diagnosed at an average age at 36 years. All patients with malignant disease underwent surgery. Four patients were found to have metastasis at the time of selective neck dissection. Among patients with malignant HNPGLs, 5 (83%) were treated with adjuvant radiation, and 1 (17%) was treated with adjuvant chemotherapy. Conclusions and Relevance: Malignant HNPGLs are rare entities that are difficult to diagnose and are typically identified by the presence of regional or distant metastasis. The results of this study found the prevalence of malignant HNPGLs to be 9%. These data suggest that it is beneficial to perform a selective neck dissection at the time of tumor excision. All patients with malignant HNPGLs but 1 had SDHB mutations.

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Year:  2019        PMID: 31194233      PMCID: PMC6567840          DOI: 10.1001/jamaoto.2019.1110

Source DB:  PubMed          Journal:  JAMA Otolaryngol Head Neck Surg        ISSN: 2168-6181            Impact factor:   6.223


  25 in total

1.  Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma.

Authors:  D Astuti; F Latif; A Dallol; P L Dahia; F Douglas; E George; F Sköldberg; E S Husebye; C Eng; E R Maher
Journal:  Am J Hum Genet       Date:  2001-06-12       Impact factor: 11.025

Review 2.  Paragangliomas of the head and neck: diagnosis and treatment.

Authors:  C C Boedeker; G J Ridder; J Schipper
Journal:  Fam Cancer       Date:  2005       Impact factor: 2.375

Review 3.  Malignant pheochromocytomas and paragangliomas: a diagnostic challenge.

Authors:  Oliver Gimm; Catherine DeMicco; Aurel Perren; Francesco Giammarile; Martin K Walz; Laurent Brunaud
Journal:  Langenbecks Arch Surg       Date:  2011-11-29       Impact factor: 3.445

Review 4.  Paragangliomas of the Head and Neck: An Overview from Diagnosis to Genetics.

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

5.  National Cancer Data Base report on malignant paragangliomas of the head and neck.

Authors:  John H Lee; Frank Barich; Lucy Hynds Karnell; Robert A Robinson; Weining K Zhen; Bruce J Gantz; Henry T Hoffman
Journal:  Cancer       Date:  2002-02-01       Impact factor: 6.860

6.  A 15-year experience with chemotherapy of patients with paraganglioma.

Authors:  S R Patel; D J Winchester; R S Benjamin
Journal:  Cancer       Date:  1995-10-15       Impact factor: 6.860

7.  Malignant head and neck paragangliomas in SDHB mutation carriers.

Authors:  Carsten Christof Boedeker; Hartmut P H Neumann; Wolfgang Maier; Birke Bausch; Jörg Schipper; Gerd Jürgen Ridder
Journal:  Otolaryngol Head Neck Surg       Date:  2007-07       Impact factor: 3.497

8.  Carotid body paraganglioma with metastases.

Authors:  P Zbaren; W Lehmann
Journal:  Laryngoscope       Date:  1985-04       Impact factor: 3.325

Review 9.  Paragangliomas of the head and neck.

Authors:  Phillip K Pellitteri; Alessandra Rinaldo; David Myssiorek; C Gary Jackson; Patrick J Bradley; Kenneth O Devaney; Ashok R Shaha; James L Netterville; Johannes J Manni; Alfio Ferlito
Journal:  Oral Oncol       Date:  2004-07       Impact factor: 5.337

10.  Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.

Authors:  Lauren Fishbein; Shana Merrill; Douglas L Fraker; Debbie L Cohen; Katherine L Nathanson
Journal:  Ann Surg Oncol       Date:  2013-03-20       Impact factor: 5.344

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  8 in total

1.  Some Considerations in Treating Malignant Head and Neck Paragangliomas.

Authors:  Abhishek Jha; Naris Nilubol; Karel Pacak
Journal:  JAMA Otolaryngol Head Neck Surg       Date:  2020-02-01       Impact factor: 6.223

Review 2.  Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Familial Tumor Syndromes.

Authors:  Vania Nosé; Alexander J Lazar
Journal:  Head Neck Pathol       Date:  2022-03-21

3.  A Carotid Body Tumour Mimicking Richter's Transformation of Chronic Lymphocytic Leukaemia.

Authors:  Younus Qamar; Maryam Gulzar; Amna Qamar; Noreen Rasheed; Imran Syed
Journal:  Cureus       Date:  2022-04-18

4.  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

5.  Role of 68Ga-DOTATATE PET/CT in a Case of SDHB-Related Pterygopalatine Fossa Paraganglioma Successfully Controlled with Octreotide.

Authors:  Abhishek Jha; Mayank Patel; Eva Baker; Melissa K Gonzales; Alexander Ling; Corina Millo; Marianne Knue; Ali Cahid Civelek; Karel Pacak
Journal:  Nucl Med Mol Imaging       Date:  2020-01-22

6.  Head and Neck Paragangliomas: Patterns of Otolaryngology Referrals for Genetic Testing Over 2 Decades.

Authors:  Joshua D Smith; Emily L Bellile; Tobias Else; Gregory Basura
Journal:  OTO Open       Date:  2021-03-03

7.  Head/neck paragangliomas: focus on tumor location, mutational status and plasma methoxytyramine.

Authors:  Susan Richter; Bei Qiu; Mirthe Ghering; Carola Kunath; Georgiana Constantinescu; Charlotte Luths; Christina Pamporaki; Nicole Bechmann; Leah Meuter; Aleksandra Kwapiszewska; Timo Deutschbein; Svenja Nölting; Mirko Peitzsch; Mercedes Robledo; Aleksander Prejbisz; Karel Pacak; Volker Gudziol; Henri J L M Timmers; Graeme Eisenhofer
Journal:  Endocr Relat Cancer       Date:  2022-03-21       Impact factor: 5.678

8.  Case Report: Genetic Alterations Associated with the Progression of Carotid Paraganglioma.

Authors:  Vladislav Pavlov; Anastasiya Snezhkina; Dmitry Kalinin; Alexander Golovyuk; Anastasiya Kobelyatskaya; Ildar Bakhtogarimov; Nadezhda Volchenko; George Krasnov; Anna Kudryavtseva
Journal:  Curr Issues Mol Biol       Date:  2021-12-17       Impact factor: 2.976

  8 in total

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