首页> 外文期刊>European journal of cancer: official journal for European Organization for Research and Treatment of Cancer (EORTC) [and] European Association for Cancer Research (EACR) >Raltitrexed (Tomudex) versus standard leucovorin-modulated bolus 5-fluorouracil: Results from the randomised phase III Pan-European Trial in Adjuvant Colon Cancer 01 (PETACC-1).
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Raltitrexed (Tomudex) versus standard leucovorin-modulated bolus 5-fluorouracil: Results from the randomised phase III Pan-European Trial in Adjuvant Colon Cancer 01 (PETACC-1).

机译:Raltitrexed(Tomudex)与标准亚叶酸调节的5-氟尿嘧啶推注:佐剂性结肠癌01(PETACC-1)中的随机III期泛欧洲试验结果。

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OBJECTIVES: PETACC-1 assessed if raltitrexed is non-inferior to 5-fluorouracil and leucovorin for relapse-free survival (RFS) and overall survival (OS) in adjuvant stage III colon cancer. METHODS: Non-inferiority required both HR for RFS and OS<1.25 at 1-sided alpha=0.05. Patients (1921) were randomised to six cycles of 5-FU/LV (n=969) or eight cycles of raltitrexed (n=952). We report the final results in 993 eligible patients who started and completed the allocated treatment (489 5-FU/LV and n=504 Raltitrexed) of whom respectively 146 and 148 died, respectively. RESULTS: The trial closed prematurely when 17 (1.9%) raltitrexed-related deaths were reported. Haematological and gastrointestinal toxicities were more frequent with 5-FU/LV, liver toxicities with raltitrexed. Raltitrexed was stopped for toxicity in 13.2% and 5-FU/LV in 8.5%. Sixty-day mortality was 9% versus 7%. With 4.1 years median follow-up, the HR for RFS was 1.16 (90% CI 0.99-1.37) and that for OS was 1.01 (90% CI 0.84-1.23). CONCLUSION:The trial failed to demonstrate non-inferiority of raltitrexed. FUNDING: Free drugs and financial support from AstraZeneca.
机译:目的:PETACC-1评估了雷替曲塞在辅助性III期结肠癌中的无复发生存期(RFS)和总生存期(OS)是否不低于5-氟尿嘧啶和亚叶酸。方法:非劣效性要求RFS的HR和OS <1.25且单侧alpha = 0.05。患者(1921)被随机分为6个周期的5-FU / LV(n = 969)或8个周期的雷替曲塞(n = 952)。我们报告了993名合格患者的最终结果,这些患者开始和完成了分配的治疗(489 5-FU / LV,n = 504 Raltitrexed),分别死亡146和148。结果:该试验过早结束,原因是报告了17例(1.9%)与雷公tre有关的死亡。 5-FU / LV的血液和胃肠道毒性更高,拉替曲塞的肝脏毒性更高。停止使用Raltitrexed的毒性为13.2%,而5-FU / LV的毒性为8.5%。六十天死亡率为9%,而同期为7%。经过4.1年的中位随访,RFS的HR为1.16(90%CI 0.99-1.37),而OS的HR为1.01(90%CI 0.84-1.23)。结论:该试验未能证明拉替曲非劣效性。资金:阿斯利康提供免费药物和财务支持。

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