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(18)F-FDG PET/CT成像在接受mTOR抑制剂治疗的恶性PEComa患者中的作用。

The role of (18)F-FDG PET/CT imaging in patient with malignant PEComa treated with mTOR inhibitor.

作者信息

Sun Lu, Sun Xiaorong, Li Yuhui, Xing Ligang

机构信息

School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Jinan, Shandong, People's Republic of China.

PET/CT Center, Department of Radiology, Shandong Cancer Hospital and Institute, Jinan, Shandong, People's Republic of China.

出版信息

Onco Targets Ther. 2015 Jul 30;8:1967-70. doi: 10.2147/OTT.S85444. eCollection 2015.

Abstract

Malignant perivascular epithelioid cell tumor (malignant PEComa) is a rare disease for which the diagnostic criteria and treatment options have not been established. Since PEComa is associated with upregulation of mammalian target of rapamycin (mTOR) pathway which controls Glut-1 (glucose transporter) function, increased (18)F-fluorodeoxyglucose ((18)F-FDG) uptake may indicate the over activation of mTOR pathway and may guide selectively inhibiting mTOR pathway treatment. We report a malignant PEComa patient who presented for (18)F-FDG positron emission tomography/computed tomography (PET/CT) restaging. The tumor had shown significant avidity on PET/CT as well as an evident response to sirolimus (rapamycin, Rapamune™) that supports the utility of mTOR inhibitors as an effective treatment for malignant PEComa. Therefore, (18)F-FDG PET/CT is helpful in restaging and guiding treatment for malignant PEComa with mTOR inhibitors.

摘要

恶性血管周上皮样细胞瘤(恶性PEComa)是一种罕见疾病,其诊断标准和治疗方案尚未确立。由于PEComa与控制Glut-1(葡萄糖转运蛋白)功能的雷帕霉素哺乳动物靶点(mTOR)通路的上调有关,(18)F-氟脱氧葡萄糖((18)F-FDG)摄取增加可能表明mTOR通路过度激活,并可能指导选择性抑制mTOR通路治疗。我们报告了一名因(18)F-FDG正电子发射断层扫描/计算机断层扫描(PET/CT)进行再分期的恶性PEComa患者。该肿瘤在PET/CT上显示出明显的摄取,并对西罗莫司(雷帕霉素,Rapamune™)有明显反应,这支持了mTOR抑制剂作为恶性PEComa有效治疗方法的实用性。因此,(18)F-FDG PET/CT有助于恶性PEComa的再分期以及指导使用mTOR抑制剂进行治疗。

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