Multicenter phase II study of fixed sequences of capecitabine combined with oxaliplatin or irinotecan in patients with previously untreated metastatic colorectal cancer

被引:6
作者
Cassinello, Javier
Valero Alvarez, Jose
Garcia Lopez, Maria Jose
Pujol, Eduardo
Colmenarejo, Antonio
Segovia, Femando
Marcos, Fernando
Filipovich, Elena
Arcediano, Alberto
Garcia Castro, Ines
机构
[1] Hosp Univ Guadalajara, Med Oncol Serv, Guadalajara 19002, Spain
[2] Hosp Rodriguez Chamorro, Zamora, Spain
[3] Hosp Nuestra Senora Alarcos, Ciudad Real, Spain
[4] Hosp Santa Barbara, Soria, Spain
[5] Hosp Nuestra Senora Prado, Talavera De La Reina, Spain
[6] Hosp Nuestra Senora Sonsoles, Avila, Spain
关键词
chemotherapy; hematologic toxicity; neutropenia; thrombocytopenia;
D O I
10.3816/CCC.2006.n.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The purpose of this study was to evaluate the antitumor activity and toxicity of fixed sequences of capecitabine/oxaliplatin followed by capecitabine/irinotecan in patients with previously untreated metastatic colorectal cancer. Patients and Methods: Adult patients with histologically confirmed, previously untreated, nonresectable, locally advanced or metastatic colorectal adenocarcinoma were enrolled in the study. Patients were treated as follows: capecitabine (1000 mg/m(2) orally twice daily) on days 1-14 and oxaliplatin (130 mg/m(2) 2-hour intravenous infusion) on day 1, followed by capecitabine (1000 mg/m(2) twice daily) on days 1-14 and irinotecan (240 mg/m(2) 1.5-hour intravenous infusion) on day 1. Each combination was administered every 21 days during 4 consecutive cycles followed by the alternating sequence to a maximum of 16 cycles. Results: A total of 35 eligible patients have been included in this ongoing study. Response rate (complete responses plus partial responses) was 37.1%.With a median follow-up of 9.5 months, the median time to disease progression and overall survival were 7.4 months and 16.4 months, respectively. Treatment was well tolerated, with only 6% of the patients developing grade 3/4 neurotoxicity, However, the low number of patients treated beyond 4 cycles limits the interpretation of the data. Conclusion: The preliminary results from this ongoing study suggest the feasibility of this strategy, which resulted in promising antitumor activity with less neurotoxicity.
引用
收藏
页码:429 / 435
页数:7
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