弥合癌症研究临床前和临床研究之间的差距

R. Kumari
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引用次数: 0

摘要

几十年来,随着新技术的出现,癌症研究领域已经达到了成功的顶峰。尽管癌症基础和临床前研究取得了成功,但大多数临床试验并没有取得预期结果。基本上,临床前研究在决定一种药物是否安全、有效并准备好进行临床试验时发挥着极其重要的作用。通过临床前研究评估人类特效药对临床试验的成功至关重要。不幸的是,临床前癌症研究的可译性明显低于其他治疗领域[1-2]。癌症的临床试验失败率最高,这是一个公认的事实。事实上,设计临床试验所依据的许多重要的临床前发现实际上是不可重复的[1]。因此,迫切需要重新审视癌症临床前的研究策略,以取得更大的临床成功。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bridging the Gap between Pre-Clinical and Clinical Studies in Cancer Research
With the advent of new technologies over the decades the field of Cancer Research has reached its pinnacle of success. Despite the success of basic and pre-clinical cancer research most of the clinical trials do not succeed with expected outcome. Basically, pre-clinical studies play an enormously important role when it comes to decide whether a drug is safe, effective, and ready for clinical trials or not. The evaluation of human specific drugs through pre-clinical studies is extremely crucial for the success of clinical trials. Unfortunately, the translatability of pre-clinical cancer research is significantly low than other therapeutic areas [1-2]. It is now a well-established fact that the clinical trials in cancer have the highest failure rate. Indeed, many significant pre-clinical findings based on which the clinical trials are designed are not actually reproducible [1]. Consequently, there is an urgent need to revisit the pre-clinical cancer research strategies to achieve a greater clinical success.
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