Preclinical efficacy of the c-Met inhibitor CE-355621 in a U87 MG mouse xenograft model evaluated by 18F-FDG small-animal PET.

JOURNAL OF NUCLEAR MEDICINE(2008)

引用 69|浏览5
暂无评分
摘要
The purpose of this study was to evaluate the efficacy of CE-355621, a novel antibody against c-Met, in a subcutaneous U87 MG xenograft mouse model using F-18-FDG small-animal PET. Methods: CE-355621 or control vehicle was administered intraperitoneally into nude mice (drug-treated group, n = 12; control group, n = 14) with U87 MG subcutaneous tumor xenografts. Drug efficacy was evaluated over 2 wk using F-18-FDG small-animal PET and compared with tumor volume growth curves. Results:The maximum %ID/g (percentage injected dose per gram of tissue) of F-18-FDG accumulation in mice treated with CE-355621 remained essentially unchanged over 2 wk, whereas the %ID/g of the control tumors increased 66% compared with the baseline. Significant inhibition of F-18-FDG accumulation was seen 3 d after drug treatment, which was earlier than the inhibition of tumor volume growth seen at 7 d after drug treatment. Conclusion: CE-355621 is an efficacious novel antineoplastic chemotherapeutic agent that inhibits F-18-FDG accumulation earlier than tumor volume changes in a mouse xenograft model. These results support the use of F-18-FDG PET to assess early tumor response for CE-355621.
更多
查看译文
关键词
CE-355621,c-Met inhibitor,F-18-FDG,microPET,drug evaluation,therapy response
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要