Bridging the Gap between Pre-Clinical and Clinical Studies in Cancer Research

R. Kumari
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Abstract

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.
弥合癌症研究临床前和临床研究之间的差距
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。
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