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首页> 外文期刊>World Journal of Gastroenterology >Bevacizumab plus infusional 5-fluorouracil, leucovorin and irinotecan for advanced colorectal cancer that progressed after oxaliplatin and irinotecan chemotherapy: A pilot study
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Bevacizumab plus infusional 5-fluorouracil, leucovorin and irinotecan for advanced colorectal cancer that progressed after oxaliplatin and irinotecan chemotherapy: A pilot study

机译:奥沙利铂和伊立替康化疗后进展的晚期大肠癌贝伐单抗加5-氟尿嘧啶,亚叶酸钙和伊立替康的输注:一项初步研究

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AIM: To evaluate the combination of bevacizumab with infusional 5-fluorouracil (5-FU), leucovorin (LV) and irinotecan (FOLFIRI) in patients with advanced colorectal cancer (CRC) pretreated with combination regimens including irinotecan and oxaliplatin. METHODS: Fourteen patients (median age 56 years) with advanced CRC, all having progressed after oxaliplatin- and irinotecan-based combination chemotherapy, were enrolled in this study. Patients were treated with 2 h infusion of irinotecan 150 mg/m~2 on d 1, plus bevacizumab 5 mg/kg iv infusion for 90 min on d 2, and iv injection of LV 20 mg/m~2 followed by a bolus of 5-FU 400 mg/m~2 and then 22 h continuous infusion of 600 mg/m~2 given on two consecutive days every 14 d. RESULTS: The median number of cycles of chemotherapy was six (range 3-12). The response rate was 28.5%, one patient had a complete response, and three patients had a partial response. Eight patients had stable disease. The median time to progression was 3.9 mo (95% CI 2.0-8.7), and the median overall survival was 10.9 mo (95% CI 9.6-12.1). Grade 3/4 neutropenia occurred in five patients, and two of these developed neutropenic fever. Grade 3 hematuria and hematochezia occurred in one. Grade 2 proteinuria occurred in two patients. However, hypertension, bowel perforation or thromboembolic events did not occur in a total of 90 cycles. CONCLUSION: Bevacizumab with FOLFIRI is well tolerated and a feasible treatment in patients with heavily treated advanced CRC.
机译:目的:评估贝伐单抗与5-氟尿嘧啶(5-FU),亚叶酸钙(LV)和伊立替康(FOLFIRI)输注的联合用药,其中包括采用伊立替康和奥沙利铂联合治疗方案的晚期结直肠癌(CRC)患者。方法:本研究纳入了14例中位年龄为56岁的晚期CRC患者,所有患者均在以奥沙利铂和伊立替康为基础的联合化疗后进展。在第1天,患者接受2个小时的伊立替康150 mg / m〜2输注治疗,再于第2天,对贝伐单抗5 mg / kg静脉输注治疗90分钟,然后静脉注射LV 20 mg / m〜2,然后再推注5-FU 400 mg / m〜2,然后每14天连续两天连续22 h连续输注600 mg / m〜2。结果:化疗的中位周期数为六个(范围3-12)。缓解率为28.5%,一名患者完全缓解,三名患者部分缓解。 8例患者病情稳定。中位进展时间为3.9个月(95%CI 2.0-8.7),中位总生存期为10.9个月(95%CI 9.6-12.1)。 3/4例中性粒细胞减少症发生在5例患者中,其中2例发展为中性粒细胞减少症。 3级血尿和便血合二为一。两名患者发生2级蛋白尿。然而,高血压,肠穿孔或血栓栓塞事件在总共90个周期中并未发生。结论:贝伐单抗联合FOLFIRI具有良好的耐受性,在重度CRC患者中是可行的治疗方法。

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