Heinicke T, Wardelmann E, Sauerbruch T, Tschampa H J, Glasmacher A, Palmedo H
Departments of Internal Medicine I, University of Bonn, Bonn, Germany.
Anticancer Res. 2005 Nov-Dec;25(6C):4591-4.
To investigate whether 18F-FDG-PET allows early assessment of response to imatinib mesylate in GIST patients.
Five gastrointestinal stromal tumour (GIST) patients and one patient with a KIT-positive small cell cancer were studied. Treatment consisted of 400 mg imatinib mesylate daily. 18F-deoxyglucose-positron emission tomography (18F-FDG-PET) scans were done before and one week after starting imatinib mesylate therapy.
Metabolic responses were detected after only one week of therapy in all GIST patients (four partial and one complete response). The mean decrease of the standardised uptake value was 60% (range 43 to 77%). In contrast, the tumour of the non-GIST patient was metabolically stable. Four of the 5 GIST patients achieved a partial response on CT after a mean duration of 23 weeks (range 6 to 48 weeks).
18F-FDG-PET is a valuable method for the detection of response to imatinib mesylate in patients with KIT-positive tumours as early as one week after starting therapy.
研究18F-FDG-PET是否能早期评估伊马替尼甲磺酸盐对胃肠道间质瘤(GIST)患者的疗效。
对5例胃肠道间质瘤患者和1例KIT阳性小细胞癌患者进行研究。治疗方案为每日口服400mg伊马替尼甲磺酸盐。在开始伊马替尼甲磺酸盐治疗前及治疗1周后进行18F-脱氧葡萄糖正电子发射断层扫描(18F-FDG-PET)。
所有GIST患者在治疗仅1周后即检测到代谢反应(4例部分缓解,1例完全缓解)。标准化摄取值的平均下降率为60%(范围43%至77%)。相比之下,非GIST患者的肿瘤代谢稳定。5例GIST患者中有4例在平均23周(范围6至48周)后CT检查显示部分缓解。
18F-FDG-PET是一种有价值的方法,可在开始治疗1周后早期检测KIT阳性肿瘤患者对伊马替尼甲磺酸盐的反应。