Castiello Luciano, Santodonato Laura, Napolitano Mariarosaria, Carlei Davide, Montefiore Enrica, Monque Domenica Maria, D'Agostino Giuseppina, Aricò Eleonora
Cell Factory FaBioCell, Core Facilities, Italian National Institute of Health, 00161 Rome, Italy.
Research Coordination and Support Service, Italian National Institute of Health, 00161 Rome, Italy.
Cancers (Basel). 2022 Oct 30;14(21):5351. doi: 10.3390/cancers14215351.
Chimeric antigen receptor T cell therapies are revolutionizing the clinical practice of hematological tumors, whereas minimal progresses have been achieved in the solid tumor arena. Multiple reasons have been ascribed to this slower pace: The higher heterogeneity, the hurdles of defining reliable tumor antigens to target, and the broad repertoire of immune escape strategies developed by solid tumors are considered among the major ones. Currently, several CAR therapies are being investigated in preclinical and early clinical trials against solid tumors differing in the type of construct, the cells that are engineered, and the additional signals included with the CAR constructs to overcome solid tumor barriers. Additionally, novel approaches in development aim at overcoming some of the limitations that emerged with the approved therapies, such as large-scale manufacturing, duration of manufacturing, and logistical issues. In this review, we analyze the advantages and challenges of the different approaches under development, balancing the scientific evidences supporting specific choices with the manufacturing and regulatory issues that are essential for their further clinical development.
嵌合抗原受体T细胞疗法正在彻底改变血液肿瘤的临床实践,而在实体肿瘤领域取得的进展却微乎其微。造成这种进展缓慢的原因有很多:较高的异质性、确定可靠的肿瘤抗原作为靶点的障碍,以及实体肿瘤所采用的广泛的免疫逃逸策略被认为是主要原因。目前,几种嵌合抗原受体疗法正在针对实体肿瘤进行临床前和早期临床试验研究,这些疗法在构建体类型、经过基因改造的细胞以及嵌合抗原受体构建体中包含的额外信号等方面存在差异,目的是克服实体肿瘤障碍。此外,正在研发的新方法旨在克服已获批疗法中出现的一些局限性,如大规模生产、生产持续时间和后勤问题。在这篇综述中,我们分析了正在研发的不同方法的优势和挑战,在支持特定选择的科学证据与对其进一步临床开发至关重要的生产和监管问题之间取得平衡。