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首页> 外文期刊>Investigational new drugs. >A phase I/II trial of celecoxib with chemotherapy and radiotherapy in the treatment of patients with locally advanced oesophageal cancer.
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A phase I/II trial of celecoxib with chemotherapy and radiotherapy in the treatment of patients with locally advanced oesophageal cancer.

机译:塞来昔布联合化疗和放疗在局部晚期食道癌患者中进行的I / II期试验。

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摘要

BACKGROUND: The study's aim was to determine the maximum tolerated dose (MTD) of celecoxib combined with chemoradiotherapy (CRT) for locally advanced oesophageal cancer (OC). METHODS: CRT comprised of 5FU (1000 mg/m(2)/day, days 1-4, weeks 1 & 5), cisplatin (75 mg/m(2), days 1 & 29) and radiotherapy (50 Gy in 25 fractions or 50.4 Gy in 28 fractions). Celecoxib was given daily during CRT at one of five doses (200 mg bd to 600 mg bd). Three to six patients were assigned per dose. RESULTS: Thirteen patients were recruited before trial closure due to external safety concerns regarding celecoxib. Median follow up was 17 months (95% CI 9 - >39). The highest administered dose was 400 mg bd (n=4) with one dose-limiting toxicity at this level: grade 3 rash. Five (38%) and 8(62%) patients had grade 3 non-haematological and haematological toxicities respectively. No grade 4 toxicities occurred. Radiological response rate was 54% (n=7: all CR). Six patients had resection with one pathological CR. Median progression-free and overall survival were 8.8 (95% CI 5.1 - >24.8) and 19.6 months (95% CI 7.3 - >39) respectively. CONCLUSIONS: A MTD was not reached. The regimen was tolerable, indicating that celecoxib can be safely administered with CRT for locally advanced OC.
机译:背景:这项研究的目的是确定塞来昔布联合放化疗(CRT)用于局部晚期食管癌(OC)的最大耐受剂量(MTD)。方法:CRT包括5FU(1000 mg / m(2)/天,第1-4天,第1和5周),顺铂(75 mg / m(2),第1和29天)和放疗(25中的50 Gy)馏分或28馏分中的50.4 Gy)。 CRT期间每天以五种剂量之一(200 mg bd至600 mg bd)给予塞来昔布。每剂分配三至六名患者。结果:由于有关塞来昔布的外部安全问题,在试验结束前招募了13名患者。中位随访时间为17个月(95%CI 9-> 39)。最高给药剂量为400 mg bd(n = 4),在此水平具有一种剂量限制性毒性:3级皮疹。分别有5名(38%)和8(62%)患者具有3级非血液学和血液学毒性。没有发生4级毒性。放射反应率为54%(n = 7:全部CR)。 6例患者切除了1例病理CR。中位无进展生存期和总生存期分别为8.8(95%CI 5.1-> 24.8)和19.6个月(95%CI 7.3-> 39)。结论:未达到MTD。该方案是可以耐受的,这表明塞来昔布可以与CRT一起安全地用于局部晚期OC。

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