Irinotecan, oxaliplatin plus bolus 5-fluorouracil and low dose folinic acid every 2 weeks - A feasibility study in metastatic colorectol cancer patients

被引:7
作者
Martinez, J
Martin, C
Chacon, M
Korbenfeld, E
Bella, S
Senna, S
Richardet, E
Coppola, F
Bas, C
Hidalgo, J
Escobar, E
Reale, M
Smilovich, AM
Wasserman, E
机构
[1] Cvitkovic Assoc Consultants Argentina, Buenos Aires, DF, Argentina
[2] Hosp Britanico, Buenos Aires, DF, Argentina
[3] Inst A Fleming, Buenos Aires, DF, Argentina
[4] Hosp Italiano Cordoba, Cordoba, Argentina
[5] Hosp Aleman Buenos Aires, Buenos Aires, DF, Argentina
[6] COIR, Mendoza, Argentina
[7] Pfizer Argentina, Buenos Aires, DF, Argentina
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 2006年 / 29卷 / 01期
关键词
oxaliplatin; irinotecan; triple combination; metastatic colorectal cancer;
D O I
10.1097/01.coc.0000196200.49373.d5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Irinotecan or oxaliplatin combined with 5-fluorouracil (5-FU) +/- folinic acid (FA) has changed the treatment standards for metastatic colorectal cancer (CRC). The oxaliplatin and irinotecan combination has reported consistent activity. The purpose of this phase II study was to assess the efficacy and safety of the simultaneous administration of a triple chemotherapy combination of oxaliplatin, irinotecan, 5-FU bolus, and FA. Materials and Methods: Eligible patients had metastatic CRC with no prior oxaliplatin or irinotecan-based chemotherapy. Treatment consisted of oxaliplatin 85 mg/m(2) followed by irinotecan 150 mg/m(2), repeated every 15 days, with 5-FU 500 mg/m(2) bolus and FA 20 mg/m(2) on days 1, 8, and 15. An early amendment suppressed the day 8 5-FU/FA. Results: Twenty-six eligible treated patients receiving 253 doses were assessed for toxicity. Myelosuppression was the most frequent toxicity; grade 3 to 4 neutropenia and febrile neutropenia occurred in 50% and 15% of patients, respectively. The treatment schedule modification, omitting the 5-FU dosing on day 8, considerably improved treatment compliance, reducing the incidence of febrile neutropenia, diarrhea, and asthenia. Among the 25 patients evaluable for efficacy, 10 had objective responses including 1 complete response (CR) (4%) and 9 partial responses (PR) (36%), giving an overall response rate of 40%. Median time to progression was 6.20 months [95% confidence interval (CI), 5.44-6.96]. Median overall survival was 12.95 months. Conclusions: The administration of a triple combination produced promising objective responses with acceptable toxicity but does not seem to produce an evident benefit in time-related parameters.
引用
收藏
页码:45 / 51
页数:7
相关论文
共 23 条
  • [21] Combination of oxaliplatin plus irinotecan in patients with gastrointestinal tumors:: Results of two independent phase I studies with pharmacokinetics
    Wasserman, E
    Cuvier, C
    Lokiec, F
    Goldwasser, F
    Kalla, S
    Méry-Mignard, D
    Ouldkaci, M
    Besmaine, A
    Dupont-André, G
    Mahjoubi, M
    Marty, M
    Misset, JL
    Cvitkovic, E
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (06) : 1751 - 1759
  • [22] Sequence- and region-specificity of oxaliplatin adducts in naked and cellular DNA
    Woynarowski, JM
    Chapman, WG
    Napier, C
    Herzig, MCS
    Juniewicz, P
    [J]. MOLECULAR PHARMACOLOGY, 1998, 54 (05) : 770 - 777
  • [23] Zeghari-Squalli N, 1999, CLIN CANCER RES, V5, P1189