4.7 Article

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

Journal

JOURNAL OF NUCLEAR MEDICINE
Volume 49, Issue 1, Pages 129-134

Publisher

SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.106.038836

Keywords

CE-355621; c-Met inhibitor; F-18-FDG; microPET; drug evaluation; therapy response

Funding

  1. NATIONAL CANCER INSTITUTE [R24CA092862] Funding Source: NIH RePORTER
  2. NCI NIH HHS [R24 CA092862, R24CA92862] Funding Source: Medline

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available