Hirsch Steffen, Marshall Lynley V, Carceller Lechon Fernando, Pearson Andrew D J, Moreno Lucas
The Royal Marsden NHS Foundation Trust, Children and Young People's Unit , Sutton, Surrey, SM2 5PT , UK +44 0 20 8915 6161 ;
Expert Opin Drug Discov. 2015 May;10(5):483-95. doi: 10.1517/17460441.2015.1025745. Epub 2015 Apr 3.
Cancer is a leading cause of death in childhood. Encouraging progress has been made in the treatment of childhood malignancies, but there is an unmet need for new drugs to improve survival and reduce treatment-associated toxicities. Drug development in paediatric oncology has specific requirements with regard to the patient population and the regulatory background and presents several unique challenges that need addressing.
This review discusses the current framework of paediatric oncology drug development and some of the specific challenges in pre-clinical and clinical research. The authors discuss the recent developments in the targeting of various signalling pathways. These pathways represent a selection of targets that have been identified by pre-clinical and clinical investigators to be highly relevant in paediatric malignancies.
The development of targeted agents in paediatric oncology must be driven by knowledge of tumour biology. Predictive and pharmacodynamic biomarkers should be incorporated within paediatric early clinical trials wherever possible. Faster dose-escalation, limited numbers of cohorts and novel adaptive designs can help to make paediatric early clinical trials more efficient. Close collaboration between academic/clinical researchers, the pharmaceutical industry, regulatory bodies and parent groups are crucial in overcoming the challenges associated with paediatric oncology drug development.
癌症是儿童死亡的主要原因。儿童恶性肿瘤的治疗已取得令人鼓舞的进展,但仍需要新药物来提高生存率并降低治疗相关毒性。儿科肿瘤学的药物开发在患者群体和监管背景方面有特定要求,并存在一些需要解决的独特挑战。
本综述讨论了儿科肿瘤学药物开发的当前框架以及临床前和临床研究中的一些特定挑战。作者讨论了各种信号通路靶向方面的最新进展。这些通路代表了临床前和临床研究人员已确定在儿科恶性肿瘤中高度相关的一系列靶点。
儿科肿瘤学中靶向药物的开发必须以肿瘤生物学知识为驱动。只要有可能,应在儿科早期临床试验中纳入预测性和药效学生物标志物。更快的剂量递增、有限数量的队列和新颖的适应性设计有助于提高儿科早期临床试验的效率。学术/临床研究人员、制药行业、监管机构和家长团体之间的密切合作对于克服与儿科肿瘤学药物开发相关的挑战至关重要。