A randomised phase II study of oxaliplatin alone versus oxaliplatin combined with 5-fluorouracil and folinic acid (Mayo Clinic regimen) in previously untreated metastatic colorectal cancer patients

被引:38
作者
Comba, AZ
Blajman, C
Richardet, E
Bella, S
Vilanova, M
Cóppola, F
Van Kooten, M
Rodger, J
Giglio, R
Balbiani, L
Perazzo, F
Montiel, M
Chacón, M
Pujol, F
Mickiewicz, E
Cazap, E
Recondo, G
Lastiri, F
Simon, J
Wasserman, E
Schmilovich, A
机构
[1] Hosp Zubizarreta, Buenos Aires, DF, Argentina
[2] Hosp Italiano, Cordoba, Argentina
[3] Clin Independencia, Buenos Aires, DF, Argentina
[4] Hosp Aleman, Buenos Aires, DF, Argentina
[5] Inst Alexander Fleming, Buenos Aires, DF, Argentina
[6] Inst Estevez, Buenos Aires, DF, Argentina
[7] Inst Angel Roffo, Buenos Aires, DF, Argentina
[8] Hosp Municipal Oncol, Buenos Aires, DF, Argentina
[9] CEMIC, Buenos Aires, DF, Argentina
[10] Acad Nacl Med Buenos Aires, Dept Bioestadiast, Buenos Aires, DF, Argentina
[11] Cvitkovic & Associates Consultants, Buenos Aires, DF, Argentina
[12] Lab Searle, Buenos Aires, DF, Argentina
关键词
colorectal; chemotherapy; oxaliplatin; Mayo clinic regimen; randomised;
D O I
10.1016/S0959-8049(01)00080-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to examine the efficacy and safety of both oxaliplatin as a single agent and oxaliplatin in combination with daily x 5 bolus 5-fluorouracil and folinic acid (5-FU/FA, Mayo clinic regimen) in the first-line treatment of metastatic colorectal cancer (CRC) patients. 73 advanced CRC patients were randomised to receive either oxaliplatin 85 mg/m(2) every 2 weeks (35 patients), or the same treatment combined with 5-FU 425 mg/m(2)/day and FA 20 mg/m(2)/day x 5 days every 4 weeks (38 patients). Treatment was continued until disease progression or unacceptable toxicity. All patients had documented inoperable disease and no previous chemotherapy for advanced disease. Based on the investigators' assessment of best response, objective response rate was 9% (95% confidence interval (CI) 2-24%) in the oxaliplatin arm, and 45% (95% CI 27-64%) in the oxaliplatin + 5-FU/FA arm. Median progression-free survival(PFS) was 2 months (95% CI 1.7-2.4 months) in the oxaliplatin arm and 3.9 months (95% CI 2.9-5 months) in the oxaliplatin + 5-FU/FA arm. Severe neutropenia was seen in 23% of patients in the oxaliplatin + 5-FU/FA arm, and none in the oxaliplatin arm. There were two treatment-related deaths, both in the oxaliplatin + 5-FU/FA arm. In the oxaliplatin + 5-FU/FA arm, severe diarrhoea, vomiting and stomatitis were seen in 34, 14 and 14% of the patients, respectively. In conclusion, oxaliplatin at a dose of 85 mg/m(2) given every 2 weeks was well tolerated and has limited activity in metastatic CRC, while the combination of this treatment with the full-dose Mayo clinic regimen (5-FU bolus 425 mg/m(2)/day + FA 20 mg/m(2)/day x 5 days every 4 weeks), although active, was unfeasible due to a high level of myelosuppression and gastrointestinal toxicity. Alternative lower dosing or other regimens are to be explored to ascertain the value of bolus 5-FU/FA combined with oxaliplatin. (C) 2001 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1006 / 1013
页数:8
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