Reduced Risk of Corporal Tumors in Patients With Head and Neck Paragangliomas With p.Pro81Leu Mutations

Author:

Miller Katherine M.1,Sbeih Firas1,Contrera Kevin2,Reddy Chandana A.3,Marquard Jessica4,Eng Charis4567,Lorenz Robert R.1

Affiliation:

1. Head and Neck Institute, Cleveland Clinic Head & Neck Institute Cleveland Ohio USA

2. Department of Head and Neck Surgery The University of Texas MD Anderson Cancer Center Houston Texas USA

3. Department of Radiation Oncology, Taussig Cancer Institute Cleveland Clinic Cleveland Ohio USA

4. Genomic Medicine Institute, Lerner Research Institute Cleveland Clinic Cleveland Ohio USA

5. Taussig Cancer Institute Cleveland Clinic Cleveland Ohio USA

6. Department of Genetics and Genome Sciences Case Western Reserve University School of Medicine Cleveland Ohio USA

7. Department of Genetics and Genome Sciences, Germline High Risk Cancer Focus Group, CASE Comprehensive Cancer Center Case Western Reserve University Cleveland Ohio USA

Abstract

AbstractObjectivePatients with head and neck paragangliomas who are positive for the SDHD p.Pro81Leu (P81L) mutation are thought to have a distinct phenotype from other SDHx mutations, but few studies have focused on this mutation. The objective of this study was to determine the hazard of developing a second primary, metastatic, or recurrent paraganglioma in SDHx patients with or without P81L.Study DesignRetrospective chart review of 60 patients with head and neck paragangliomas and genetic testing, followed for a median of 9 years.SettingSingle academic medical center.MethodsUnivariable Cox proportional hazards regression evaluated second primary and recurrent paragangliomas in patients with SDHD P81L, SDHx non‐P81L, and nonhereditary paraganglioma.ResultsThis series comprised 31 patients without SDHx, 14 with SDHD P81L, and 15 with other SDHx mutations. At a median 9 years of follow‐up, corporal (not head and neck) second primary paragangliomas occurred in 31% of patients with SDHx non‐P81L mutations, compared with 0% and 4% of patients with SDHD P81L and without SDHx mutations, respectively. Second corporal paragangliomas were more likely in patients with SDHx non‐P81L mutations than in those without a mutation (hazard ratio = 5.461, 95% confidence interval: 0.596‐50.030, p = .13).ConclusionThis is the first study to report a lower likelihood of corporal tumors for patients with head and neck paragangliomas with SDH mutations positive for P81L. Larger studies are needed to determine if head and neck paraganglioma patients with P81L qualify for less intensive imaging surveillance to screen for second primary paragangliomas outside the head and neck.

Publisher

Wiley

Subject

Otorhinolaryngology,Surgery

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