首页> 外文期刊>Anti-cancer drugs >Overcoming resistance to chronomodulated 5-fluorouracil and folinic acid by the addition of chronomodulated oxaliplatin in advanced colorectal cancer patients.
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Overcoming resistance to chronomodulated 5-fluorouracil and folinic acid by the addition of chronomodulated oxaliplatin in advanced colorectal cancer patients.

机译:在晚期结直肠癌患者中,通过添加经时脉调制的奥沙利铂,克服了对经时脉调制的5-氟尿嘧啶和亚叶酸的耐药性。

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摘要

The addition of oxaliplatin (L-OHP) to a 5-fluorouracil (5-FU)/ leucovorin (FA) regimen was retrospectively evaluated in 35 consecutive advanced colorectal cancer patients after progression of disease. L-OHP, 25 mg/m2/day, was infused from 10.00-22.00 with a peak flow at 16.00 while 5-FU, 700 mg/m2/day and FA, 150 mg/m2/day of the I-form or 300 mg/m2/day of the racemic form, from 22.00 to 10.00 with a nocturnal peak at 4.00, for 5 days every 3 weeks in 24 patients and for 4 days every 2 weeks in the other 11. Diarrhea and sensitive neuropathy were the most relevant types of toxicity (17% of patients). An objective response was achieved in 8/35 patients (23%) [95% CL 9-37], stabilization in 15 patients (43%) which included five minor responses, and progression in 12. There was no relevant difference in quality of life assessed with the EORTC QLQ C30+3 questionnaire before and after treatment. Median duration of response and median progression-free survival were 6 months; median overall survival was 11 months. This retrospective study showed that it is possible to reverse resistance to chronomodulated 5-FU by adding chronomodulated L-OHP to the previous regimen; comparison with different schedules of this combination should be performed in order to identify the best tolerated and active regimen as second-line treatment of advanced colorectal cancer.
机译:回顾性评估了疾病进展后连续35例晚期结直肠癌患者在5-氟尿嘧啶(5-FU)/亚叶酸(FA)方案中添加奥沙利铂(L-OHP)的情况。从10.00-22.00注入25 mg / m2 /天的L-OHP,峰值流量为16.00,而I型的5-FU,700 mg / m2 /天和FA,150 mg / m2 /天或300注入外消旋形式的mg / m2 /天,从22.00至10.00,夜间峰值在4.00,在24位患者中每3周持续5天,在其他11位患者中每2周持续4天。毒性类型(占患者的17%)。 8/35例患者(23%)[95%CL 9-37]达到客观缓解,15例患者(43%)达到稳定,其中包括5例轻微缓解,12例进展。治疗前后用EORTC QLQ C30 + 3问卷评估生活。中位反应持续时间和中位无进展生存期为6个月;中位总生存期为11个月。这项回顾性研究表明,通过在以前的治疗方案中添加同步L-OHP,可以逆转对5-FU的耐药性。为了确定最佳耐受性和有效方案作为晚期大肠癌的二线治疗,应与该组合的不同方案进行比较。

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