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首页> 外文期刊>Japanese journal of clinical oncology. >Oxaliplatin, folinic acid and 5-fluorouracil (FOLFOX-4) combination chemotherapy as second-line treatment in advanced colorectal cancer patients with irinotecan failure: a Korean single-center experience.
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Oxaliplatin, folinic acid and 5-fluorouracil (FOLFOX-4) combination chemotherapy as second-line treatment in advanced colorectal cancer patients with irinotecan failure: a Korean single-center experience.

机译:奥沙利铂,亚叶酸和5-氟尿嘧啶(FOLFOX-4)联合化学疗法作为伊立替康衰竭的晚期大肠癌患者的二线治疗:韩国单中心经验。

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OBJECTIVE: This study was designed to determine the effectiveness and tolerance of oxaliplatin, folinic acid (FA) and infusional 5-fluorouracil (5-FU) (FOLFOX-4) chemotherapy when used as a second-line treatment in patients with advanced colorectal cancer for whom an irinotecan-containing regimen failed. METHODS: Thirty-eight patients with measurable colorectal cancer, progressive after previous irinotecan-containing chemotherapy for metastatic disease, were registered in this trial. Oxaliplatin was administered on day 1 at the dose of 85 mg/m(2) as a 2 h infusion, concurrently with FA 200 mg/m(2)/day, followed by bolus 5-FU 400 mg/m(2) and a 22 h infusion of 5-FU 600 mg/m(2) for two consecutive days. The treatment was repeated every 2 weeks until disease progression or unacceptable toxicity occurred or until a patient chose to discontinue the treatment. RESULTS: For 34 patients treated, a total of 183 chemotherapy cycles were administered. In an intent-to-treat analysis, six patients (16%) achieved a partial response that they maintained for 5.4 months. The median progression-free and overall survivals were 2 and 5 months, respectively. Frequently encountered toxicities were peripheral neuropathy and gastrointestinal side effects including diarrhea. Although there was one early death, toxicity profiles were generally predictable and manageable. CONCLUSION: Second-line FOLFOX-4 is a feasible regimen with modest activity for colorectal cancer patients with irinotecan failure. Further clinical trials incorporating novel biological agents are warranted.
机译:目的:本研究旨在确定奥沙利铂,亚叶酸(FA)和输注5-氟尿嘧啶(5-FU)(FOLFOX-4)化疗作为晚期大肠癌患者的二线治疗的有效性和耐受性为此,含伊立替康的治疗方案失败了。方法:38例可测量的结直肠癌患者在先前接受含伊立替康的转移性疾病化疗后进展。奥沙利铂在第1天以85 mg / m(2)的剂量输注2 h,并与FA 200 mg / m(2)/ day并发,随后推注5-FU 400 mg / m(2)和连续两天连续22小时输注5-FU 600 mg / m(2)。每2周重复治疗一次,直到疾病进展或出现不可接受的毒性或直到患者选择中止治疗为止。结果:对于34例接受治疗的患者,总共进行了183个化疗周期。在意向治疗分析中,有6名患者(16%)达到了部分反应,并维持了5.4个月。中位无进展生存期和总生存期分别为2个月和5个月。常见的毒性反应是周围神经病和胃肠道副作用,包括腹泻。尽管有一个早期死亡,但毒性特征通常是可以预测和控制的。结论:二线FOLFOX-4是治疗伊立替康衰竭的大肠癌患者可行的,中等活性的方案。纳入新的生物制剂的进一步临床试验是有保证的。

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