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在复发性高级别胶质瘤的治疗监测中,3'-去氧-3'-18F-氟代胸苷的动力学。

Kinetics of 3'-deoxy-3'-18F-fluorothymidine during treatment monitoring of recurrent high-grade glioma.

机构信息

Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, University of California, Los Angeles, California 90095-6942, USA.

出版信息

J Nucl Med. 2010 May;51(5):720-7. doi: 10.2967/jnumed.109.068361. Epub 2010 Apr 15.

Abstract

UNLABELLED

3'-Deoxy-3'-(18)F-fluorothymidine ((18)F-FLT) is used as a biomarker of cell proliferation. We investigated the kinetics of (18)F-FLT during treatment of malignant glioma with bevacizumab and irinotecan.

METHODS

Fifteen patients with recurrent high-grade brain tumors (2 grade III, 13 grade IV) were studied at baseline (study 1 [S1]), after 1 course of therapy (2 wk, study 2 [S2]), and at the end of therapy (6 wk, study 3 [S3]). (18)F-FLT (1.5 MBq/kg) was administered intravenously, and dynamic PET was performed for 1 h. Curves representing blood clearance and tumor uptake were derived from factor images and summed frames with thresholding techniques or with a fixed cube. The standard (18)F-FLT model was used to estimate the rate constants. (18)F-FLT uptake was measured at 2 time points (early standardized uptake value [SUV(early)] and late SUV [SUV(late)]).

RESULTS

Parameters appeared similar for curves derived from factor images and summed frames; the steepest drop occurred between S1 and S2 for transport, influx, SUV(early), and SUV(late). Three groups were distinguished on the basis of clinical outcome: patients who died within 6 mo (group 1 [G1], n = 4), survived 6-12 mo (group 2 [G2], n = 6), and survived more than 1 y (group 3 [G3], n = 5). None of the rate constants was significantly different between the groups. Long-term survivors (G3) showed a significantly different SUV change (in percentage) between S1 and S3, whereas short-term survivors (G1 and G2) did not.

CONCLUSION

Overall, the relative SUV change from S1 to S3 predicted a favorable clinical outcome, whereas the SUV change from S1 to S2 did not. Long-term survivors (G3) showed a significant drop in SUV from S1 to S2 and from S1 to S3. Significant correlations were found between SUV and both the rate constant and the influx rate. The correlation coefficient between SUV(late) and influx rate was 0.91, permitting response monitoring by the measurement of (18)F-FLT uptake changes.

摘要

目的

研究贝伐单抗联合伊立替康治疗恶性胶质瘤过程中 3'-脱氧-3'-(18)F-氟代胸苷((18)F-FLT)的动力学。

方法

15 例复发性高级别脑肿瘤患者(2 例 3 级,13 例 4 级)在基线(研究 1[S1])、1 个疗程后(2 周,研究 2[S2])和治疗结束时(6 周,研究 3[S3])进行研究。静脉注射(18)F-FLT(1.5MBq/kg),行 1 小时动态 PET。利用因子图像和阈值技术或固定立方体生成的总和帧,得到代表血清除和肿瘤摄取的曲线。采用标准(18)F-FLT 模型估算速率常数。在 2 个时间点测量(18)F-FLT 摄取量(早期标准化摄取值[SUV(early)]和晚期 SUV[SUV(late)]。

结果

来源于因子图像和总和帧的曲线参数相似;在 S1 和 S2 之间,转运、内流、SUV(early)和 SUV(late)的下降最明显。根据临床结果将患者分为 3 组:6 个月内死亡的患者(G1,n=4)、存活 6-12 个月的患者(G2,n=6)和存活超过 1 年的患者(G3,n=5)。各组间各速率常数无显著差异。长期存活者(G3)S1 和 S3 间 SUV 变化百分比差异显著,而短期存活者(G1 和 G2)则无差异。

结论

S1 到 S3 的相对 SUV 变化总体预测临床结局良好,而 S1 到 S2 的 SUV 变化则无预测作用。长期存活者(G3)S1 到 S2 和 S1 到 S3 的 SUV 均明显下降。SUV 与速率常数和内流率均有显著相关性。SUV(late)与内流率的相关系数为 0.91,通过测量(18)F-FLT 摄取变化可监测反应。

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