TY - JOUR
T1 - Factors predicting efficacy of oxaliplatin in combination with 5-fluorouracil (5-FU) ± folinic acid in a compassionate-use cohort of 481 5-FU-resistant advanced colorectal cancer patients
AU - Bensmane, M. A.
AU - Marty, M.
AU - De Gramont, A.
AU - Brienza, S.
AU - Lévi, F.
AU - Ducreux, M.
AU - François, E.
AU - Gamelin, E.
AU - Bleiberg, H.
AU - Cvitkovic, E.
N1 - Funding Information:
This work was sponsored in part by grants from Debiopharm (Lausanne, Switzerland) and Sanofi-Synthelabo (Paris, France). We would like to thank Dr Bruno Lhote for his support of this project, and Mariko Johnson for her help in preparing the manuscript.
PY - 2001/8/17
Y1 - 2001/8/17
N2 - A statistical analysis was performed on the patient data collected from two compassionate-use programmes using oxaliplatin (Eloxatin®) + 5-fluorouracil (5-FU) ± folinic acid (FA), to identify predictive factors for oxaliplatin-based salvage treatment in patients with 5-FU-resistant advanced colorectal cancer (ACRC). 481 5-FU-resistant ACRC patients, most with performance status ≤ 2, ≥ 3 involved sites, and ≥ 2 prior lines of chemotherapy, received oxaliplatin + 5-FU ± FA. Prognostic factors associated with overall response rate (ORR), time to progression (TTP) and overall survival (OS) were identified using univariate and multivariate logistic and/or Cox proportional hazards analyses. The ORR was 16% (95% Cl: 13-20), the median TTP was 4.2 months (95% Cl: 3.4-4.6), and the median OS was 9.6 months (95% Cl: 8.6-10.6). The multivariate analysis indicated poor (≥ 2 WHO) performance status (PS), a large number of prior chemotherapy regimens (≥ 3), a low baseline haemoglobin level (< 10 g/dl), and a triweekly (vs biweekly) treatment administration schedule as significantly associated (P < 0.05) with a lower ORR. Sex (male), number of organs involved (≥3) and alkaline phosphatase (AP) level (≥ 2 × the upper limit of normal) were associated (P < 0.05) with shorter TTP. Poor PS, a large number of organs involved, and elevated AP were independently and significantly correlated with shorter OS. Our analysis identified a relationship between efficacy results of oxaliplatin + 5-FU ± FA treatment in 5-FU-resistant ACRC patients and baseline prognostic factors related to PS, extent of disease and number of prior regimens.
AB - A statistical analysis was performed on the patient data collected from two compassionate-use programmes using oxaliplatin (Eloxatin®) + 5-fluorouracil (5-FU) ± folinic acid (FA), to identify predictive factors for oxaliplatin-based salvage treatment in patients with 5-FU-resistant advanced colorectal cancer (ACRC). 481 5-FU-resistant ACRC patients, most with performance status ≤ 2, ≥ 3 involved sites, and ≥ 2 prior lines of chemotherapy, received oxaliplatin + 5-FU ± FA. Prognostic factors associated with overall response rate (ORR), time to progression (TTP) and overall survival (OS) were identified using univariate and multivariate logistic and/or Cox proportional hazards analyses. The ORR was 16% (95% Cl: 13-20), the median TTP was 4.2 months (95% Cl: 3.4-4.6), and the median OS was 9.6 months (95% Cl: 8.6-10.6). The multivariate analysis indicated poor (≥ 2 WHO) performance status (PS), a large number of prior chemotherapy regimens (≥ 3), a low baseline haemoglobin level (< 10 g/dl), and a triweekly (vs biweekly) treatment administration schedule as significantly associated (P < 0.05) with a lower ORR. Sex (male), number of organs involved (≥3) and alkaline phosphatase (AP) level (≥ 2 × the upper limit of normal) were associated (P < 0.05) with shorter TTP. Poor PS, a large number of organs involved, and elevated AP were independently and significantly correlated with shorter OS. Our analysis identified a relationship between efficacy results of oxaliplatin + 5-FU ± FA treatment in 5-FU-resistant ACRC patients and baseline prognostic factors related to PS, extent of disease and number of prior regimens.
KW - Clinical resistance
KW - Multivariate analysis
KW - Salvage chemotherapy
UR - http://www.scopus.com/inward/record.url?scp=17944376134&partnerID=8YFLogxK
U2 - 10.1054/bjoc.2001.1953
DO - 10.1054/bjoc.2001.1953
M3 - Article
C2 - 11506488
AN - SCOPUS:17944376134
SN - 0007-0920
VL - 85
SP - 509
EP - 517
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 4
ER -