Wang Zhenguang, Han Weidong
Molecular & Immunological Department, Bio-therapeutic Department, Chinese PLA General Hospital, No. 28 Fuxing Road, Beijing, 100853 China.
Biomark Res. 2018 Jan 22;6:4. doi: 10.1186/s40364-018-0116-0. eCollection 2018.
Severe cytokine release syndrome (CRS) and neurotoxicity following chimeric antigen receptor T cell (CAR-T) therapy can be life-threatening in some cases, and management of those toxicities is still a great challenge for physicians. Researchers hope to understand the pathophysiology of CRS and neurotoxicity, and identify predictive biomarkers that can forecast those toxicities in advance. Some risk factors for severe CRS and/or neurotoxicity including patient and treatment characteristics have been identified in multiple clinical trials of CAR-T cell therapy. Moreover, several groups have identified some predictive biomarkers that are able to determine beforehand which patients may suffer severe CRS and/or neurotoxicity during CAR-T cell therapy, facilitating testing of early intervention strategies for those toxicities. However, further studies are needed to better understand the biology and related risk factors for CRS and/or neurotoxicity, and determine if those identified predictors can be extrapolated to other series. Herein, we review the pathophysiology of CRS and neurotoxicity, and summarize the progress of predictive biomarkers to improve CAR-T cell therapy in cancer.
嵌合抗原受体T细胞(CAR-T)治疗后出现的严重细胞因子释放综合征(CRS)和神经毒性在某些情况下可能危及生命,对这些毒性的管理仍然是医生面临的巨大挑战。研究人员希望了解CRS和神经毒性的病理生理学,并识别能够提前预测这些毒性的生物标志物。在CAR-T细胞治疗的多项临床试验中,已经确定了一些严重CRS和/或神经毒性的风险因素,包括患者和治疗特征。此外,一些研究小组已经识别出一些预测性生物标志物,这些生物标志物能够预先确定哪些患者在CAR-T细胞治疗期间可能发生严重CRS和/或神经毒性,从而便于对这些毒性进行早期干预策略的测试。然而,需要进一步研究以更好地了解CRS和/或神经毒性的生物学及相关风险因素,并确定那些已识别的预测指标是否可外推至其他队列。在此,我们综述CRS和神经毒性的病理生理学,并总结预测性生物标志物在改善癌症CAR-T细胞治疗方面的进展。