Berns Anton, Ringborg Ulrik, Celis Julio, Jönsson Bengt, Baumann Michael
European Academy of Cancer Sciences, Stockholm, Sweden.
Division of Molecular Genetics, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Mol Oncol. 2025 Jun;19(6):1553-1560. doi: 10.1002/1878-0261.70058. Epub 2025 May 21.
The development of new anticancer treatments, their clinical evaluation and introduction into the healthcare system need improvement. New drugs and cell therapies often come with significant costs for society while only marginally improving patients' survival and health-related quality-of-life. Therefore, bold, innovative clinical trials with critical assessment of the efficacy and cost-effectiveness of new preventive measures and medical treatments are needed to ensure that patients and society benefit. Drug development programmes controlled by pharma should be complemented with initiatives such as stop studies, dose reduction, combination and repurposing trials. These should be validated in academia-initiated trials supported by societal funds. Special attention should be devoted to paediatric and rare adult cancers. Comprehensive Cancer Centres (CCCs) covering the entire cancer research continuum, present throughout the EU, are critical for this. More of such centres must be established concomitantly with a robust accreditation methodology to ensure that they meet appropriate quality standards. It is crucial that funding for these initiatives, now temporarily and partially provided by the EU Cancer Mission and Europe's Beating Cancer Plan, is secured for a much longer period.
新型抗癌治疗方法的研发、临床评估以及引入医疗保健系统都需要改进。新药和细胞疗法往往给社会带来巨大成本,而对患者生存率和健康相关生活质量的改善却微乎其微。因此,需要开展大胆、创新的临床试验,对新的预防措施和医疗治疗的疗效及成本效益进行严格评估,以确保患者和社会受益。由制药公司控制的药物研发项目应辅以停药研究、剂量减少、联合用药和药物再利用试验等举措。这些举措应在由社会资金支持的学术发起的试验中得到验证。应特别关注儿童癌症和罕见成人癌症。覆盖整个癌症研究连续过程、遍布欧盟的综合癌症中心(CCC)对此至关重要。必须建立更多这样的中心,并同时采用强有力的认证方法,以确保它们符合适当的质量标准。至关重要的是,目前由欧盟癌症使命和欧洲抗癌计划临时部分提供资金的这些举措,要获得更长时间的资金保障。