Department of Radiation Oncology, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Université Paris-Sud, Orsay, France.
Clin Cancer Res. 2020 Sep 15;26(18):4723-4736. doi: 10.1158/1078-0432.CCR-19-4155. Epub 2020 May 14.
Newer technical improvements in radiation oncology have been rapidly implemented in recent decades, allowing an improved therapeutic ratio. The development of strategies using local and systemic treatments concurrently, mainly targeted therapies, has however plateaued. Targeted molecular compounds and immunotherapy are increasingly being incorporated as the new standard of care for a wide array of cancers. A better understanding of possible prior methodology issues is therefore required and should be integrated into upcoming early clinical trials including individualized radiotherapy-drug combinations. The outcome of clinical trials is influenced by the validity of the preclinical proofs of concept, the impact on normal tissue, the robustness of biomarkers and the quality of the delivery of radiation. Herein, key methodological aspects are discussed with the aim of optimizing the design and implementation of future precision drug-radiotherapy trials.
近几十年来,放射肿瘤学的新技术改进得到了迅速实施,从而提高了治疗效果。然而,同时使用局部和全身治疗(主要是靶向治疗)的策略已经达到了瓶颈。靶向分子化合物和免疫疗法越来越多地被纳入广泛癌症的治疗标准。因此,需要更好地了解可能存在的先前方法学问题,并将其纳入即将进行的早期临床试验,包括个体化放疗药物联合治疗。临床试验的结果受到临床前概念验证的有效性、对正常组织的影响、生物标志物的稳健性以及放射治疗质量的影响。本文讨论了关键的方法学方面,旨在优化未来精准药物放疗试验的设计和实施。