TY - JOUR
T1 - Factors predicting for efficacy of oxaliplatin in combination with 5-fluorouracil (5-FU)±folinic acid (FA) in a compassionate-use cohort of 370 5-FU-resistant advanced colorectal cancer (CRC) patients
AU - Bensmane, M. A.
AU - De Gramont, A.
AU - Brienza, S.
AU - Marty, M.
AU - Lévi, F.
AU - Ducreux, M.
AU - François, E.
AU - Gamelin, E.
AU - Bleiberg, H.
AU - Bleuzen, P.
AU - Simon, J.
AU - Cvitkovic, E.
PY - 2000/12/5
Y1 - 2000/12/5
N2 - Univariate and multivariate analyses were performed on data from 370 5-fluorouracil (5-FU)-resistant advanced colorectal cancer patients treated with oxaliplatin (Eloxatin®)/5-FU±folinic acid (FA) to identify prognostic factors for oxaliplatin-based treatment. The response rate was 14.6% (95% confidence interval (CI): 11.0-18.2%), median time to progression was 4.3 months (95% CI: 3.9-4.7), and median overall survival 9.7 months (95% CI: 8.5-10.8). Multivariate analysis indicated < 2 prior chemotherapy regimens, bi-weekly treatment administration schedule (versus tri-weekly) and continuous chronomodulated delivery (CCM) as significantly associated (P < 0.05) with a higher overall response rate. Performance status (PS) < 2, having only one involved organ, biweekly schedule and CCM were associated (P < 0.05) with a longer time to progression. Good PS, one involved organ, low alkaline phosphatase (AP) serum levels, bi-weekly schedule and CCM were significantly correlated with longer overall survival, while confirming the efficacy of oxaliplatin/5-FU±FA in this indication. (C) 2000 Elsevier Science Ltd.
AB - Univariate and multivariate analyses were performed on data from 370 5-fluorouracil (5-FU)-resistant advanced colorectal cancer patients treated with oxaliplatin (Eloxatin®)/5-FU±folinic acid (FA) to identify prognostic factors for oxaliplatin-based treatment. The response rate was 14.6% (95% confidence interval (CI): 11.0-18.2%), median time to progression was 4.3 months (95% CI: 3.9-4.7), and median overall survival 9.7 months (95% CI: 8.5-10.8). Multivariate analysis indicated < 2 prior chemotherapy regimens, bi-weekly treatment administration schedule (versus tri-weekly) and continuous chronomodulated delivery (CCM) as significantly associated (P < 0.05) with a higher overall response rate. Performance status (PS) < 2, having only one involved organ, biweekly schedule and CCM were associated (P < 0.05) with a longer time to progression. Good PS, one involved organ, low alkaline phosphatase (AP) serum levels, bi-weekly schedule and CCM were significantly correlated with longer overall survival, while confirming the efficacy of oxaliplatin/5-FU±FA in this indication. (C) 2000 Elsevier Science Ltd.
KW - Clinical resistance
KW - Multivariate analysis
KW - Salvage chemotherapy
UR - http://www.scopus.com/inward/record.url?scp=0033695520&partnerID=8YFLogxK
U2 - 10.1016/S0959-8049(00)00305-1
DO - 10.1016/S0959-8049(00)00305-1
M3 - Article
C2 - 11094307
AN - SCOPUS:0033695520
SN - 0959-8049
VL - 36
SP - 2335
EP - 2343
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 18
ER -