A randomized phase II study of raltitrexed and gefitinib versus raltitrexed alone as second line chemotherapy in patients with colorectal cancer. (1839IL/0143)
Autor: | Luis de Sande González, José Luis García-López, Humberto Bovio, Ignacio Peláez, Manuel Valladares, Jesús García-Foncillas, Margarita Reboredo, Carlos García-Girón, Jose María Vieitez, Angel J. Lacave |
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Rok vydání: | 2010 |
Předmět: |
Adult
Male Oncology medicine.medical_specialty Adolescent Colorectal cancer Phases of clinical research Antineoplastic Agents Thiophenes Young Adult Gefitinib Internal medicine Antineoplastic Combined Chemotherapy Protocols Biomarkers Tumor medicine Clinical endpoint Humans Pharmacology (medical) Progression-free survival Survival analysis Aged Demography Pharmacology business.industry Middle Aged medicine.disease Survival Analysis Rash Treatment Outcome Quinazolines Female medicine.symptom Colorectal Neoplasms business Raltitrexed medicine.drug |
Zdroj: | Investigational New Drugs. 29:1038-1044 |
ISSN: | 1573-0646 0167-6997 |
DOI: | 10.1007/s10637-010-9400-z |
Popis: | Purpose To determine the efficacy of the addition of gefitinib to raltitrexed in patients with colorectal cancer (CRC) that have progressed after first line chemotherapy. The study also sought to explore the safety of the combination and to investigate biomarkers predictive outcome. Methods A total of 76 patients were randomized to raltitrexed (3 mg/m2 i.v.) every 21 days plus either daily gefitinib (250 mg p.o.) or placebo. The primary endpoint of the study was progression free survival (PFS). Tumor tissues were collected to determine the expression of EGFR, pEGFR, pMAPK, and pAkt. Results Both groups were well balanced with regard to prognostic factors. Treatment was well tolerated with no increased in toxicity except diarrhea and skin rash in the combination group. There were no differences in PFS between the combination arm [63 days (95% CI: 57–84)] compared to the raltitrexed alone arm [72 days (95% CI: 59–132)], or overall survival 361 days (95% CI: 283–533 days) versus 291 days (95% CI: 255–539 days) respectively. The objective response rate was 7.9% (3 patients) (CI 95%: 1,66–21,38) versus 5.3% (2 patients) (CI 0,64–17,75), respectively. The biomarker studies were not conclusive. Conclusion The combination of raltitrexed and gefitinib was well tolerated although was not associated with improved progression free survival in patients with refractory CRC. |
Databáze: | OpenAIRE |
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