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The Role of Targeted Therapy in Adjuvant Colorectal Cancer Trials: Where Did We Go Wrong and Where Do We Go from Here?

机译:有针对性治疗在佐剂结直肠癌试验中的作用:我们在哪里出错,我们从这里去哪里?

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The new biologic drugs active in the advanced setting of colorectal cancer have failed when used in the adjuvant setting. Both bevacizumab (BEVA) and cetuximab (CET) added to oxaliplatin-based chemotherapy (CT) have produced no improvements in 3-year disease-free survival (DFS) rates compared with CT alone. Even worse, the possibility exists that both agents are actually detrimental to the efficacy of CT in this setting. BEVA, after an initial impressive delay in relapses (0.6 hazard ratio [HR] for DFS at 12 months in both the NSABP C-08 and AVANT studies) did not maintain this beneficial effect; more relapses and deaths occurred, compared with CT alone in the 2 years after discontinuation of the antiangiogenic agent. The danger of a rebound effect is real.
机译:当在佐剂设置中使用时,新的生物药物活跃于结直肠癌的晚期环境失效。添加到基于Oxaliplatin的化学疗法(CT)的Bevacizumab(Beva)和西妥昔单抗(CET)都没有在与单独的CT相比的3年无病的存活率(DFS)率没有改善。更糟糕的是,存在两种药剂的可能性实际上对该环境中CT的功效有害。 BEVA,经过初步令人印象深刻的延迟(在12个月内为NSABP C-08和Avant研究中的DFS的0.6危险比[HR])并未保持这种有益效果;发生了更多的复发和死亡,与抗原试剂停止后2年中单独的CT相比。反弹效果的危险是真实的。

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