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Which Strategies Will Lead to Progress in the Management of Colorectal Cancer?

机译:哪些策略将导致结直肠癌治疗的进展?

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摘要

The past decade has seen considerable progress in the treatment of colorectal cancer (CRC) in the United States; whereas in 1996, one agent had been approved for the treatment of CRC, there are now seven approved drugs in the United States. This panoply of options now requires us to refine our approaches to therapy. It apears that the best approach would be to devote ourselves to unraveling the biology of CRC, so that we can both understand its diversity and use that understanding to individualize treatment for patients with this disease. The focus would be to maximize antitumor effects and, when possible, to minimize toxicity. Genetic analyses of tumors, the host, or both should lead to such advances, as preliminary analyses have shown. Optimizing drug combinations and minimizing toxicity has heretofore been mainly empirically rather than scientifically driven. A host of rationally designed new agents are in development. Sorting through those with clinical activity – although a difficult process – should result in additional active agents. One troubling consequence of this new drug development has been the high costs of combination therapies, which may render them unavailable to certain patient segments that could potentially benefit from them. Despite the complexities involved, the pace of progress is accelerating and sustaining that pace must be our highest priority.
机译:在过去的十年中,美国在结直肠癌(CRC)的治疗方面取得了长足的进步。而在1996年,一种药物被批准用于CRC的治疗,而美国现在有7种药物被批准。现在,这众多选择要求我们完善治疗方法。可以断定,最好的方法是致力于研究CRC的生物学,以便我们既可以了解CRC的多样性,又可以利用这种理解来个性化治疗该病的患者。重点是使抗肿瘤作用最大化,并在可能的情况下使毒性最小化。正如初步分析所表明的那样,对肿瘤,宿主或两者的遗传学分析应导致这种进展。迄今为止,优化药物组合和最小化毒性主要是凭经验而不是科学驱动的。大量设计合理的新代理正在开发中。对具有临床活动的人员进行分类(尽管过程很困难),但应得到更多的活性剂。这种新药开发的一个令人不安的后果是联合疗法的高昂费用,这可能会使某些可能无法从中受益的患者细分市场无法使用它们。尽管涉及复杂性,但进展的步伐正在加快,维持这一步伐必须是我们的最高优先事项。

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