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镓[68Ga]DOTATOC PET/CT 在肿瘤性骨软化症中的诊断性能。

Diagnostic performance of Ga-DOTATOC PET/CT in tumor-induced osteomalacia.

机构信息

Department of Diagnostic Imaging and Nuclear Medicine, Graduate School of Medicine Kyoto University, 54 Shogoinkawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.

Department of Diagnostic Imaging, Kyoto City Hospital, Kyoto, Japan.

出版信息

Ann Nucl Med. 2021 Mar;35(3):397-405. doi: 10.1007/s12149-021-01575-x. Epub 2021 Feb 13.

Abstract

OBJECTIVE

Tumor-induced osteomalacia (TIO) is caused by typically small tumors that secrete fibroblast growth factor 23 (FGF23). As tumor resection is the only effective treatment for TIO, it is important to detect the culprit tumor. We aimed to assess the utility of Gallium-DOTA-D-Phe(1)-Tyr(3)-octreotide (Ga-DOTATOC) PET/CT in TIO and the correlation between biochemical parameters and the PET/CT results.

METHODS

Thirty-five patients with clinically suspected TIO who had undergone Ga-DOTATOC PET/CT were retrospectively analyzed. Ga-DOTATOC PET/CT results were compared with biochemical parameters and the final diagnosis, including histopathology.

RESULTS

Ga-DOTATOC PET/CT detected focal uptake consistent with TIO in 21/35 patients, one of which was considered false positive. In 16 patients, the cause of osteomalacia was confirmed histologically as phosphaturic mesenchymal tumor (n = 15) or fibrous dysplasia (n = 1). The other four patients were judged clinically as true positive by subsequent MRI and the clinical course. Overall, the detection rate of Ga-DOTATOC PET/CT was 57% (20/35). Median tumor maximum standardized uptake value (SUVmax) was 6.9 (range 1.5-37.7). There was no significant difference in serum intact FGF23 level between DOTATOC-positive and DOTATOC-negative cases, and no significant correlation was observed between intact FGF23 level and tumor SUVmax.

CONCLUSIONS

Ga-DOTATOC PET/CT was clinically useful in detecting culprit tumors and subsequent patient management in TIO.

摘要

目的

肿瘤性骨软化症(TIO)由通常分泌成纤维细胞生长因子 23(FGF23)的小肿瘤引起。由于肿瘤切除是 TIO 的唯一有效治疗方法,因此检测致病肿瘤非常重要。我们旨在评估镓-DOTA-D-Phe(1)-Tyr(3)-奥曲肽(Ga-DOTATOC)PET/CT 在 TIO 中的应用价值,以及生化参数与 PET/CT 结果之间的相关性。

方法

回顾性分析 35 例临床疑似 TIO 且行 Ga-DOTATOC PET/CT 检查的患者。将 Ga-DOTATOC PET/CT 结果与生化参数和最终诊断(包括组织病理学)进行比较。

结果

Ga-DOTATOC PET/CT 在 21/35 例患者中检测到与 TIO 一致的局灶性摄取,其中 1 例被认为是假阳性。在 16 例患者中,通过组织病理学证实骨软化症的病因分别为磷酸盐尿性间质瘤(n=15)或纤维结构不良(n=1)。另外 4 例患者通过后续 MRI 和临床病程被临床判断为真正阳性。总体而言,Ga-DOTATOC PET/CT 的检出率为 57%(20/35)。肿瘤最大标准化摄取值(SUVmax)中位数为 6.9(范围 1.5-37.7)。DOTATOC 阳性和 DOTATOC 阴性病例之间血清完整 FGF23 水平无显著差异,且完整 FGF23 水平与肿瘤 SUVmax 之间无显著相关性。

结论

Ga-DOTATOC PET/CT 在 TIO 中检测致病肿瘤和后续患者管理方面具有临床应用价值。

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