From the Department of Otorhinolaryngology, Plastic, Aesthetic, and Reconstructive Head and Neck Surgery, University Hospital Würzburg.
Institute of Pathology and Comprehensive Cancer Center Mainfranken, Julius-Maximilian University Würzburg.
Clin Nucl Med. 2023 Nov 1;48(11):923-927. doi: 10.1097/RLU.0000000000004870. Epub 2023 Sep 21.
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.
Fourteen patients with HNPGL received pretherapeutic SSTR-PET/CTs using 68 Ga-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 SUV max and target-to-background ratio (TBR). Quantitative values were then compared between subgroups of patients affected with different HNPGL entities.
On visual assessment, all primary HNPGLs could be identified on SSTR-PET/CT. Quantification of HNPGL revealed substantially elevated SUV max 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.
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.
由于其神经内分泌起源,头颈部副神经节瘤(HNPGL)可以通过生长抑素受体(SSTR)导向的 PET/CT 进行成像。我们旨在确定体内 PET 信号是否可以区分不同的 HNPGL 亚型。
14 名 HNPGL 患者接受了使用 68Ga-DOTATOC 的 SSTR-PET/CT 预治疗。6 名(42.9%)患者患有颈静脉副神经节瘤(PGL-J),5 名(35.7%)患者被诊断为颈动脉副神经节瘤(PGL-Cs),其余 3 名患者(21.4%)患有携带致病性 SDHx 种系变异的 PGL-C(PGL-C-SDH)。对 SSTR-PET 上的原发性肿瘤进行了视觉和定量评估,包括 SUV max 和靶标与背景比(TBR)。然后将具有不同 HNPGL 实体的患者亚组之间的定量值进行了比较。
在视觉评估中,SSTR-PET/CT 可以识别所有原发性 HNPGL。HNPGL 的定量显示,与 PGL-C-SDH(13.4 ± 5.6,P < 0.05)相比,PGL-J 的 SUV max 明显升高(101.7 ± 58.5),但与 PGL-C(66.7 ± 27.3,P = 0.4)相比则不然,与 PGL-C-SDH(P = 0.2)相比也是如此。然而,PGL-J 的 TBR(202.9 ± 82.2)进一步区分了 PGL-C(95.7 ± 45.4,P < 0.05)和 PGL-C-SDH(20.4 ± 12.2,P < 0.01;PGL-C 与 PGL-C-SDH,P = 0.3)。此外,全身阅读显示 2/3(66.7%)的 PGL-C-SDH 患者有转移,其中 1 例患者有单一 SSTR 表达的骨骼病变,另 1 例患者有双肺病变。
在 HNPGL 患者中,SSTR-PET/CT 可识别原发性和转移性疾病,并提供明显升高的 TBR,表明图像对比度极佳。基于 PET 的定量还可以区分不同的 HNPGL 亚型。