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Oxaliplatin and protracted venous infusion of 5-fluorouracil in patients with advanced or relapsed 5-fluorouracil pretreated colorectal cancer

机译:奥沙利铂和5-氟尿嘧啶预处理的晚期大肠癌或复发性结肠癌患者经长期静脉滴注5-氟尿嘧啶

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摘要

The purpose of this study was to evaluate the activity and safety of oxaliplatin and protracted venous infusion of 5-fluorouracil (PVI 5-FU) in patients with advanced or relapsed 5-FU pretreated colorectal cancer. 38 patients with advanced or metastatic colorectal carcinoma with documented progression on or within 6 months following 5-FU or thymidylate synthase inhibitor containing chemotherapy were recruited between June 1997 and September 2000. Oxaliplatin (100 mg m−2) was given every 2 weeks and PVI 5-FU (300 mg m−2day−1) was administered. Median age of patients was 61 years. 17 patients had >2 sites of disease involvement. 10 had received 5-FU based adjuvant chemotherapy. 16 received oxaliplatin and PVI 5-FU as second-line chemotherapy for advanced disease and 22 as third or subsequent lines. Median follow up was 6.1 months. The best achieved objective tumour response rate was 29% (11 partial responses 95% confidence interval [CI] = 15–46%). 20 patients (52.6%) had stable disease. The median duration of response was 3.9 months. Even for patients who had previously received both 5-FU and irinotecan (n= 22), 27.3% had partial response with oxaliplatin and PVI 5-FU. 37 patients had symptoms on entry into the study. 25 patients had pain, 10 had anorexia and 28 had lethargy. 64%, 70% and 17.9% had symptomatic improvement after treatment respectively. Grade 3–4 toxicities were anaemia 10.6%, neutropenia 2.6%, thrombocytopenia 5.2%, diarrhoea 18.9%, nausea and vomiting 2.7%, infection 5.4% and lethargy 37.8%. The median survival was 9.1 months. Probability of overall survival at 6 months was 58.4% (95% CI = 38.7–73.7%). The median failure-free survival was 4 months. Oxaliplatin and PVI 5FU is an active and well tolerated regimen in patients with heavily pre-treated advanced colorectal cancer. © 2001 Cancer Research Campaign
机译:这项研究的目的是评估晚期或复发的5-FU预处理结直肠癌患者中奥沙利铂和5-氟尿嘧啶(PVI 5-FU)长期静脉输注的活性和安全性。 1997年6月至2000年9月,招募了38名晚期或转移性结直肠癌患者,这些患者在包含5-FU或胸苷酸合酶抑制剂的化疗后6个月或6个月内进展。每2周给予一次PVI 5-FU(300μmgm -2 day -1 )。患者的中位年龄为61岁。 17名患者有2个以上的疾病受累部位。 10例接受了5-FU辅助化疗。 16例接受奥沙利铂和PVI 5-FU进行晚期疾病的二线化疗,22例接受第三线或后续治疗。中位随访时间为6.1个月。达到的最佳客观肿瘤缓解率为29%(11个局部缓解95%置信区间[CI] = 15-46%)。 20名患者(52.6%)病情稳定。中位缓解时间为3.9个月。即使是既往接受5-FU和伊立替康(22例)的患者,也有27.3%的患者接受了奥沙利铂和PVI 5-FU的部分缓解。 37名患者进入研究时出现症状。 25例患者疼痛,10例厌食,28例嗜睡。治疗后症状改善分别为64%,70%和17.9%。 3-4级毒性反应为:贫血10.6%,中性粒细胞减少症2.6%,血小板减少症5.2%,腹泻18.9%,恶心和呕吐2.7%,感染5.4%和嗜睡37.8%。中位生存期为9.1个月。 6个月时总生存概率为58.4%(95%CI = 38.7–73.7%)。中位无故障生存期为4个月。奥沙利铂和PVI 5FU是一种在严重预处理的晚期大肠癌患者中有效且耐受性良好的方案。 ©2001癌症研究运动

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