Maertens Ophélia, McCurrach Mila E, Braun Benjamin S, De Raedt Thomas, Epstein Inbal, Huang Tannie Q, Lauchle Jennifer O, Lee Hyerim, Wu Jianqiang, Cripe Timothy P, Clapp D Wade, Ratner Nancy, Shannon Kevin, Cichowski Karen
Genetics Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts.
Cancer Res. 2017 Nov 1;77(21):5706-5711. doi: 10.1158/0008-5472.CAN-17-1789. Epub 2017 Oct 9.
Preclinical studies using genetically engineered mouse models (GEMM) have the potential to expedite the development of effective new therapies; however, they are not routinely integrated into drug development pipelines. GEMMs may be particularly valuable for investigating treatments for less common cancers, which frequently lack alternative faithful models. Here, we describe a multicenter cooperative group that has successfully leveraged the expertise and resources from philanthropic foundations, academia, and industry to advance therapeutic discovery and translation using GEMMs as a preclinical platform. This effort, known as the Neurofibromatosis Preclinical Consortium (NFPC), was established to accelerate new treatments for tumors associated with neurofibromatosis type 1 (NF1). At its inception, there were no effective treatments for NF1 and few promising approaches on the horizon. Since 2008, participating laboratories have conducted 95 preclinical trials of 38 drugs or combinations through collaborations with 18 pharmaceutical companies. Importantly, these studies have identified 13 therapeutic targets, which have inspired 16 clinical trials. This review outlines the opportunities and challenges of building this type of consortium and highlights how it can accelerate clinical translation. We believe that this strategy of foundation-academic-industry partnering is generally applicable to many diseases and has the potential to markedly improve the success of therapeutic development. .
使用基因工程小鼠模型(GEMM)的临床前研究有加快有效新疗法开发的潜力;然而,它们并未常规纳入药物开发流程。GEMM对于研究不太常见癌症的治疗方法可能特别有价值,这些癌症通常缺乏其他可靠的模型。在此,我们描述了一个多中心合作组织,该组织成功利用了慈善基金会、学术界和产业界的专业知识和资源,以GEMM作为临床前平台推进治疗性发现和转化。这项工作被称为神经纤维瘤病临床前联盟(NFPC),其成立目的是加速针对与1型神经纤维瘤病(NF1)相关肿瘤的新治疗方法的研发。在其成立之初,NF1没有有效的治疗方法,且几乎没有有前景的方法。自2008年以来,参与的实验室通过与18家制药公司合作,对38种药物或药物组合进行了95项临床前试验。重要的是,这些研究确定了13个治疗靶点,这些靶点已激发了16项临床试验。本综述概述了建立此类联盟的机遇与挑战,并强调了它如何能加速临床转化。我们相信,这种基金会 - 学术界 - 产业界合作的策略普遍适用于许多疾病,并有显著提高治疗开发成功率的潜力。 。