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A randomized phase II study to compare oxaliplatin plus 5-fluorouracil and leucovorin (FOLFOX4) versus oxaliplatin plus raltitrexed (TOMOX) as first-line chemotherapy for advanced colorectal cancer
Gravalos, C; Salut, A; García-Girón, C; García-Carbonero, R; León, A. I; Sevilla, I; Maurel, J; Esteban, B; García-Rico, E; Murias, A; Cortés-Funes, H.
Affiliation
  • Gravalos, C; University Hospital 12 de Octubre. Madrid. Spain
  • Salut, A; Hospital Arnau de Vilanova. Lleida. Spain
  • García-Girón, C; Hospital General Yagüe. Burgos. Spain
  • García-Carbonero, R; Hospital Severo Ochoa. Leganés. Spain
  • León, A. I; Fundación Jiménez Díaz. Madrid. Spain
  • Sevilla, I; Hospital Virgen de la Victoria. Málaga. Spain
  • Maurel, J; Hospital Clinic i Provincial. Barcelona. Spain
  • Esteban, B; Hospital General de Segovia. Segovia. Spain
  • García-Rico, E; Hospital de Montepríncipe. Madrid. Spain
  • Murias, A; Hospital Insular de Las Palmas. Gran Canaria. Spain
  • Cortés-Funes, H; University Hospital 12 de Octubre. Madrid. Spain
Clin. transl. oncol. (Print) ; 14(8): 606-612, ago. 2012.
Article in En | IBECS | ID: ibc-126957
Responsible library: ES1.1
Localization: BNCS
ABSTRACT
INTRODUCTION: The aim of this study was to compare TOMOX versus FOLFOX4 as first-line treatment of advanced colorectal cancer (CRC). MATERIALS AND METHODS: 191 chemotherapy-naïve patients were randomized to receive TOMOX or FOLFOX4. Patients were evaluated every 3 months and chemotherapy was continued until disease progression or unacceptable toxicity. Overall response rate was the primary endpoint. RESULTS: 183 patients were included in the intent-to-treat analysis (92 TOMOX and 91 FOLFOX4). Overall response rate was 45.6 and 36.3 % (p = 0.003) for TOMOX and FOLFOX4, respectively. No statistically significant differences were observed in overall survival (15.6 and 17.2 months; p = 0.475); progression-free survival (7.7 and 8.7 months; p = 0.292), and response duration (6.4 and 7.6 months; p = 0.372) for TOMOX and FOLFOX4, respectively. Grades 3 and 4 neutropenia (p < 0.0001) and leukopenia (p = 0.028) were more common with the FOLFOX4 regimen, while hepatic disorders and asthenia were higher in TOMOX group (p = ns). There were two treatment-related deaths in the FOLFOX4 arm and one in the TOMOX arm. Quality of life analysis based on the SF-36 revealed differences between the two regimens for physical and mental composite scores after 6 weeks, and for body pain and emotional role functioning after 6 and 12 weeks; all of these favored the FOLFOX4 arm (p ≤ 0.05). CONCLUSIONS: TOMOX and FOLFOX4 seem to have similar efficacy and are well tolerated in the first-line treatment for advanced CRC with different profiles of toxicity. The convenient TOMOX regimen may offer an alternative to fluoropyrimidine-based regimens (AU)
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Collection: 06-national / ES Database: IBECS Main subject: Colorectal Neoplasms / Antineoplastic Combined Chemotherapy Protocols Type of study: Clinical_trials Aspects: Patient_preference Limits: Adult / Aged / Female / Humans / Male Language: En Journal: Clin. transl. oncol. (Print) Year: 2012 Document type: Article
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Collection: 06-national / ES Database: IBECS Main subject: Colorectal Neoplasms / Antineoplastic Combined Chemotherapy Protocols Type of study: Clinical_trials Aspects: Patient_preference Limits: Adult / Aged / Female / Humans / Male Language: En Journal: Clin. transl. oncol. (Print) Year: 2012 Document type: Article