Kairemo Kalevi, Santos Elmer B, Macapinlac Homer A, Subbiah Vivek
Department of Nuclear Medicine, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Investigational Cancer Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Diagnostics (Basel). 2020 Jan 6;10(1):26. doi: 10.3390/diagnostics10010026.
Although 2-deoxy-2-[18F]-fluoro-D-glucose positron emission tomography/computed tomography (F-FDG PET/CT) is a sensitive nuclear medicine modality, specificity for characterizing lung cancer is limited. Tumor proliferation and early response to molecularly targeted therapy could be visualized using 3'-deoxy-3'[(18)F]-fluorothymidine (F-FLT) PET/CT. The superiority of F-FLT PET/CT over F-FDG PET/CT in early therapeutic monitoring has been well described in patients after chemotherapy, radiotherapy, and/or chemo/radiotherapy. In thispilot study, we explorethe use of F-FLT PET/CT as an early response evaluation modality in patients with lung cancerand provide specific case studies of patients with small cell lung cancer and non-small cell lung cancer who received novel targeted therapies. Early response for c-MET inhibitor was observed in four weeks and for MDM2 inhibitor in nine days.
尽管2-脱氧-2-[18F]-氟-D-葡萄糖正电子发射断层扫描/计算机断层扫描(F-FDG PET/CT)是一种敏感的核医学检查方法,但用于肺癌特征性诊断的特异性有限。使用3'-脱氧-3'-[(18)F]-氟胸苷(F-FLT)PET/CT可观察到肿瘤增殖及对分子靶向治疗的早期反应。在化疗、放疗和/或放化疗后的患者中,F-FLT PET/CT在早期治疗监测方面优于F-FDG PET/CT,这一点已有充分描述。在这项前瞻性研究中,我们探索将F-FLT PET/CT用作肺癌患者早期反应评估方法,并提供接受新型靶向治疗的小细胞肺癌和非小细胞肺癌患者的具体病例研究。观察到c-MET抑制剂治疗四周出现早期反应,MDM2抑制剂治疗九天出现早期反应。
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