ACCELERATE.
Zoé4life, Switzerland.
Eur J Cancer. 2019 Mar;110:74-85. doi: 10.1016/j.ejca.2019.01.013. Epub 2019 Feb 14.
Paediatric Strategy Forums have been created by the multistakeholder organisation, ACCELERATE, and the European Medicines Agency to facilitate dialogue between all relevant stakeholders and suggest strategies in critical areas of paediatric oncology drug development. As there are many medicines being developed for B-cell malignancies in adults but comparatively few in children with these malignancies, a Paediatric Strategy Forum was held to discuss the best approach to develop these products for children. It was concluded that as current frontline therapy is highly successful, despite associated acute toxicity, de-escalation of this or substitution of presently used drugs with new medicines can only be undertaken when there is an effective salvage regimen, which is currently not available. Therefore priority should be given to developing treatment for patients with relapsed and refractory mature B-cell lymphomas. The consensus of the clinicians attending the meeting was that CAR T-cells, T-cell engagers and antibody drug conjugates (excluding those with a vinca alkaloid-like drug) presently have the greatest probability of providing benefit in relapse in view of their mechanism of action. However, as producing autologous CAR T-cells currently takes at least 4 weeks, they are not products which could be quickly employed initially at relapse in rapidly progressing mature B-cell malignancies but only for the consolidation phase of the treatment. Global, industry-supported, academic-sponsored studies testing compounds from different pharmaceutical companies simultaneously should be considered in rare populations, and it was proposed that an international working group be formed to develop an overarching clinical trials strategy for these disease groups. Future Forums are planned for other relevant paediatric oncologic diseases with a high unmet medical need and relevant molecular targets.
儿科战略论坛由多利益相关者组织 ACCELERATE 和欧洲药品管理局创建,旨在促进所有相关利益攸关方之间的对话,并为儿科肿瘤药物开发的关键领域提出策略。由于有许多药物正在为成人的 B 细胞恶性肿瘤开发,但儿童中相对较少,因此举办了一个儿科战略论坛来讨论为儿童开发这些产品的最佳方法。结论是,由于目前的一线治疗非常成功,尽管存在相关的急性毒性,但在没有有效的挽救方案的情况下,只能降低这种毒性或用新药替代目前使用的药物。因此,应优先为复发和难治性成熟 B 细胞淋巴瘤患者开发治疗方法。参加会议的临床医生的共识是,鉴于其作用机制,CAR T 细胞、T 细胞激动剂和抗体药物偶联物(不包括具有长春花生物碱样药物的那些)目前最有可能在复发时提供获益。然而,由于目前生产自体 CAR T 细胞至少需要 4 周,因此它们不是在快速进展的成熟 B 细胞恶性肿瘤复发时最初可以快速使用的产品,而只是用于治疗的巩固阶段。应考虑在罕见人群中同时进行全球、行业支持、学术赞助的研究,以测试来自不同制药公司的化合物,有人提议成立一个国际工作组,为这些疾病群体制定总体临床试验策略。未来还计划为其他具有高未满足医疗需求和相关分子靶点的相关儿科肿瘤疾病举办论坛。