Somatostatin Receptor–Directed PET/CT Can Differentiate Between Different Subtypes of Head and Neck Paragangliomas

Author:

Zhi Yingjun1,Gerhard-Hartmann Elena2,Hartrampf Philipp E.3,Weich Alexander,Higuchi Takahiro,Bley Thorsten A.4,Hackenberg Stephan5,Hagen Rudolf1,Rosenwald Andreas2,Scherzad Agmal1,Remde Hanna6,Fassnacht Martin6,Werner Rudolf A.,Serfling Sebastian E.

Affiliation:

1. Department of Otorhinolaryngology, Plastic, Aesthetic, and Reconstructive Head and Neck Surgery, University Hospital Würzburg

2. Institute of Pathology and Comprehensive Cancer Center Mainfranken, Julius-Maximilian University Würzburg

3. Department of Nuclear Medicine

4. Department of Diagnostic and Interventional Radiology, University Hospital Würzburg, Würzburg

5. Department of Otorhinolaryngology–Head and Neck Surgery, RWTH Aachen University, Aachen

6. Division of Endocrinology, Department of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany

Abstract

Background Given their neuroendocrine origin, head and neck paragangliomas (HNPGLs) can be imaged with somatostatin receptor (SSTR)–directed PET/CT. We aimed to determine whether the in vivo PET signal can differentiate between varying HNPGL subtypes. Patients and Methods Fourteen patients with HNPGL received pretherapeutic SSTR-PET/CTs using 68Ga-DOTATOC. Six (42.9%) patients had a jugular paraganglioma (PGL-J), 5 (35.7%) were diagnosed with carotid paraganglioma (PGL-Cs), and the remaining 3 patients (21.4%) had PGL-C with pathogenic SDHx germline variants (PGL-C-SDH). A visual and quantitative assessment of the primary tumor on SSTR-PET was performed, including SUVmax and target-to-background ratio (TBR). Quantitative values were then compared between subgroups of patients affected with different HNPGL entities. Results On visual assessment, all primary HNPGLs could be identified on SSTR-PET/CT. Quantification of HNPGL revealed substantially elevated SUVmax in PGL-J (101.7 ± 58.5) when compared with PGL-C-SDH (13.4 ± 5.6, P < 0.05), but not when compared with PGL-C (66.7 ± 27.3, P = 0.4; PGL-C vs PGL-C-SDH, P = 0.2). TBR of PGL-J (202.9 ± 82.2), however, further differentiated between PGL-C (95.7 ± 45.4, P < 0.05) and PGL-C-SDH (20.4 ± 12.2, P < 0.01; PGL-C vs PGL-C-SDH, P = 0.3). Moreover, whole-body readout revealed metastases in 2/3 (66.7%) of PGL-C-SDH patients, with a single SSTR-expressing skeletal lesion in one subject and bipulmonary lesions in the other patient. Conclusions In patients with HNPGL, SSTR-PET/CT identified the primary and metastatic disease and provides substantially elevated TBR, indicating excellent image contrast. PET-based quantification can also differentiate between varying HNPGL subtypes.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Radiology, Nuclear Medicine and imaging,General Medicine

Reference29 articles.

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