Pfizer Inc, New York, NY, USA.
Pfizer Inc, La Jolla, CA, USA.
Paediatr Drugs. 2021 Jul;23(4):381-394. doi: 10.1007/s40272-021-00455-1. Epub 2021 Jun 26.
Regulatory changes have been enacted in the United States (US) and European Union (EU) to encourage the development of new treatments for pediatric cancer. Here, we review some of the factors that have hampered the development of pediatric cancer treatments and provide a comparison of the US and EU regulations implemented to address this clinical need. We then provide some recommendations for each stage of the oncology drug development pathway to help researchers maximize their chance of successful drug development while complying with regulations. A key recommendation is the engagement of key stakeholders such as regulatory authorities, pediatric oncologists, academic researchers, patient advocacy groups, and a Pediatric Expert Group early in the drug development process. During drug target selection, sponsors are encouraged to consult the Food and Drug Administration (FDA), European Medicines Agency (EMA), and the FDA target list, in addition to relevant US and European consortia that have been established to characterize and prioritize oncology drug targets. Sponsors also need to carefully consider the resourcing requirements for preclinical testing, which include ensuring appropriate access to the most relevant databases, clinical samples, and preclinical models (cell lines and animal models). During clinical development, sponsors can account for the pharmacodynamic (PD)/pharmacokinetic (PK) considerations specific to a pediatric population by developing pediatric formulations, selecting suitable PD endpoints, and employing sparse PK sampling or modeling/simulation of drug exposures where appropriate. Additional clinical considerations include the specific design of the clinical trial, the potential inclusion of children in adult trials, and the value of cooperative group trials.
美国(US)和欧盟(EU)已颁布监管法规,以鼓励开发新的儿科癌症治疗方法。在这里,我们回顾了一些阻碍儿科癌症治疗开发的因素,并比较了为满足这一临床需求而实施的美国和欧盟法规。然后,我们针对肿瘤药物开发途径的每个阶段提出了一些建议,以帮助研究人员在遵守法规的同时,最大限度地提高药物开发成功的机会。一个关键建议是在药物开发过程的早期让关键利益相关者(如监管机构、儿科肿瘤学家、学术研究人员、患者权益团体和儿科专家组)参与进来。在药物靶点选择阶段,鼓励赞助商咨询美国食品药品监督管理局(FDA)、欧洲药品管理局(EMA)和 FDA 靶点清单,以及为了对肿瘤药物靶点进行特征描述和优先级排序而建立的相关美国和欧洲联盟。赞助商还需要仔细考虑临床前测试的资源需求,包括确保能够适当获取最相关的数据库、临床样本和临床前模型(细胞系和动物模型)。在临床开发过程中,赞助商可以通过开发儿科制剂、选择合适的 PD 终点以及在适当情况下采用稀疏 PK 采样或药物暴露建模/模拟,来考虑儿科人群特有的药效学(PD)/药代动力学(PK)因素。其他临床考虑因素包括临床试验的具体设计、儿童在成人试验中的潜在纳入以及合作组试验的价值。