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首页> 外文期刊>Journal of Clinical Oncology >Biweekly chemotherapy with oxaliplatin, irinotecan, infusional Fluorouracil, and leucovorin: a pilot study in patients with metastatic colorectal cancer.
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Biweekly chemotherapy with oxaliplatin, irinotecan, infusional Fluorouracil, and leucovorin: a pilot study in patients with metastatic colorectal cancer.

机译:奥沙利铂,伊立替康,氟尿嘧啶和亚叶酸静脉输注的双周化疗:转移性结直肠癌患者的初步研究。

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PURPOSE: To determine the feasibility, recommended doses, plasma pharmacokinetics, and antitumor activity of a biweekly chemotherapy regimen with oxaliplatin (L-OHP), irinotecan (CPT-11), infusional fluorouracil (5-FU), and leucovorin (LV) in metastatic colorectal cancer patients. PATIENTS AND METHODS: Patients received CPT-11 followed by L-OHP and LV 200 mg/m(2) and followed by 5-FU 3,800 mg/m(2) as a 48-hour infusion, repeated every 2 weeks. In the first part of the study, an escalation of CPT-11 dose and/or a decrease of the L-OHP dose were planned. Once the recommended doses of CPT-11 and L-OHP were determined, all subsequent patients were treated at the recommended doses. RESULTS: Forty-two patients entered the study. CPT-11 175 mg/m(2) and L-OHP 100 mg/m(2) in combination with LV 200 mg/m(2) and 5-FU 3,800 mg/m(2) could be administered with acceptable toxicities; 39 patients were treated at these dose levels. The pharmacokinetics parameters of the agents used and their metabolites did not seem to be influenced by the concomitant use of the other drugs. The most relevant toxicities were diarrhea and neutropenia, with 14% of patients experiencing one episode of febrile neutropenia. In five patients (11.9%) a complete and in 25 (59.5%) a partial response was demonstrated, for an objective response rate of 71.4% (95% confidence interval, 47% to 83%). In 11 patients (26%), a surgical resection of residual disease could be performed. Median progression-free and overall survival times were 10.4 and 26.5 months, respectively. CONCLUSION: This biweekly regimen is feasible and has acceptable and manageable toxicities and no apparent relevant pharmacokinetics interactions. This combination is associated with a promising antitumor activity, time to progression, and survival. A phase III randomized trial in Italy planned by the Gruppo Oncologico Nord Ovest has just started.
机译:目的:为确定每两周一次的奥沙利铂(L-OHP),伊立替康(CPT-11),输注氟尿嘧啶(5-FU)和亚叶酸(LV)化疗方案的可行性,建议剂量,血浆药代动力学和抗肿瘤活性转移性结直肠癌患者。患者与方法:患者接受CPT-11治疗,随后接受L-OHP和LV 200 mg / m(2),然后接受48小时输注的5-FU 3,800 mg / m(2),每2周重复一次。在研究的第一部分中,计划提高CPT-11剂量和/或降低L-OHP剂量。一旦确定了CPT-11和L-OHP的推荐剂量,所有随后的患者都将以推荐剂量接受治疗。结果:42例患者进入研究。可以将CPT-11 175 mg / m(2)和L-OHP 100 mg / m(2)与LV 200 mg / m(2)和5-FU 3,800 mg / m(2)结合使用,并具有可接受的毒性;在这些剂量水平下治疗了39名患者。所用药物及其代谢产物的药代动力学参数似乎不受其他药物同时使用的影响。最相关的毒性反应是腹泻和中性粒细胞减少,其中14%的患者经历了一次发热性中性粒细胞减少。在5例患者中(11.9%),完全缓解;在25例患者中(59.5%),部分缓解,客观缓解率为71.4%(95%置信区间,47%至83%)。在11例患者(26%)中,可以对残留疾病进行手术切除。无进展中位生存时间和总生存时间分别为10.4和26.5个月。结论:这种每两周一次的方案是可行的,并且具有可接受和可控制的毒性,并且没有明显的相关药代动力学相互作用。这种组合与有希望的抗肿瘤活性,进展时间和存活率有关。 Gruppo Oncologico Nord Ovest计划在意大利进行的一项III期随机试验刚刚开始。

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