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[Cancer Research 62, 5778-5784, October 15, 2002]
© 2002 American Association for Cancer Research


Experimental Therapeutics

Cyclooxygenase-2 Inhibition with Celecoxib Enhances Antitumor Efficacy and Reduces Diarrhea Side Effect of CPT-11

Ovidiu C. Trifan1, William F. Durham, Valerie S. Salazar, Jennifer Horton, Benjamin D. Levine, Ben S. Zweifel, Thomas W. Davis and Jaime L. Masferrer

Oncology Pharmacology, Pharmacia Corp., Chesterfield, Missouri 63198

Combining anticancer drugs with different mechanisms of action has the potential to enhance antitumor effect. CPT-11 (Camptosar, irinotecan), a topoisomerase I inhibitor, has been shown to be highly effective in the treatment of a variety of cancers. However, its clinical usage is often complicated by late diarrhea. A number of studies have shown that cyclooxygenase (COX)-2 is overexpressed in many forms of human tumors, suggesting that COX-2 inhibition may be useful in the treatment of cancer. In this study, we used two mouse tumor models (HT-29 and colon-26 cells) to evaluate the effect of combining CPT-11 with celecoxib on tumor growth. We also assessed the involvement of COX-2 in the pathogenesis of CPT-11-induced late diarrhea using a rat model. Results indicate that celecoxib enhances the antitumor effect of CPT-11 and reduces the severity of late diarrhea in a dose-dependent manner. The extended benefits of combining celecoxib with CPT-11 may significantly improve the outcome of cancer patients.




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Copyright © 2002 by the American Association for Cancer Research.