MedicineOncologyPharmacologyCancer PharmacologyChemotherapyMedical OncologyColorectal CancerCombination ChemotherapyCytotoxic ChemotherapyPharmacodynamics Of Anticancer DrugsAnticancer ChemotherapyColorectal Cancer PrognosisCurative TherapyImmunohistochemical BiomarkersImmunohistochemical DetectionImmunohistochemical MarkersImmunohistochemical StainingShort-term Efficacy Evaluation
This study investigated the antitumour and chemosensitizing effects of celecoxib in the treatment of advanced colorectal cancer. A total of 90 patients were randomly divided into two groups: group CF was treated with a combination of celecoxib and the folinic acid-fluorouracil-oxaliplatin (FOLFOX4) regimen; and group F was treated with the FOLFOX4 regimen alone. Immunohisto chemical analysis of tumour tissues for cyclooxygenase-2 (COX-2) protein was performed. With regard to short-term efficacy, the response and disease control rates were significantly greater in group CF than group F. A log-rank test showed that the 3-year survival rate was significantly greater in group CF than group F. It was concluded that the addition of celecoxib to the FOLFOX4 regimen increased the short-term efficacy and the 3-year survival rate, and improved the quality of life of patients with advanced colorectal cancer. The antitumour and chemo sensitizing effects of celecoxib appeared to be independent of COX-2.
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COX-2 is expressed in human pulmonary, colonic, and mammary tumors
Robert A. Soslow, Andrew J. Dannenberg, Demaretta Rush et al. · Cancer · 2000 · 872 citations
Host cyclooxygenase-2 modulates carcinoma growth
Christopher S. Williams, Masahiko Tsujii, Jeff Reese et al. · Journal of Clinical Investigation · 2000 · 677 citations · Full text
Medicine, Oncology, Pharmacology +17