Xiao X, Yuan T, Meng J X, Jiang Y Y, Cao Y Q, Li Q, Sun R, Zhao M F
Graduate School, Tianjin Medical University, Tianjin 300070, China, is now working at the Department of Hematology, Tianjin First Central Hospital.
Department of Hematology, Tianjin. First Central Hospital, Tianjin 300192, China.
Zhonghua Yi Xue Za Zhi. 2020 Mar 3;100(8):593-598. doi: 10.3760/cma.j.issn.0376-2491.2020.08.006.
To investigate the factors influencing the efficacy of CD19 chimeric antigen receptor T (CAR-T) cells in the treatment of patients with relapsed refractory B cell lymphoma and to provide evidence for further improvement of CAR-T efficacy. A total of 34 patients with relapsed and refractory B-cell lymphoma were recruited from the Department of Hematology of Tianjin First Central Hospital from February 2017 to January 2019. All patients received CD19 CAR-T cell therapy. These patients were evaluated for efficacy, factors with poor efficacyand adverse effects. The overall response rate was 58.8% (20/34) and the complete remission rate was 41.2% (14/34) after infusion of CD19 CAR-T cells in 34 patients with relapsed refractory B cell lymphoma. According to the efficacy of CAR-T cells, patients were divided into two groups, 20 in the effective group and 14 in the poorly effective group. The median am ount of CD19 CAR-T cell infusions in these two groups were 8.6 (5.0-12.7)×10(6)/kg and 9.7 (5.8-15.0) × 10(6)/kg, respectively, and the difference was not statistically significant (0.654). The percentage of CD19 CAR-T cells in the effective group and the poorly treated group was 10.28% (3.92%-44.16%) and 4.05% (0.92%-28.63%), respectively.The effective group had a higher proportion of CAR-T cells than the poorly treated group, but the difference was not statistically significant (0.371).The presence of massive mass was an unfavorable factor affecting the efficacy of CD19 CAR-T cells and the difference was statistically significant (0.001). Logistic regression multivariate analysis showed that the characteristics of massive tumors were still independent prognostic factors for poor efficacy of CD19 CAR-T cells (0.005, 0.039). Of all 34 patients, there were 70.6% (24/34) who showed varying degrees of adverse reactions after the infusion of CD19 CAR-T cells, mainly cytokines release syndrome (CRS). The median time of occurrence of fever was on the third day after infusion (0-11th) day. 16 patients were with grade 1 CRS, 7 with grade 2, and 1 with grade 3. After glucocorticoids and support treatment, they all showed improvements. CD19 CAR-T cell therapy has achieved a certain effect in CD19(+)B cell lymphoma, but has poor efficacy on some patients. Large mass tumors may be an adverse factors to CAR-T cell treatment.
探讨影响CD19嵌合抗原受体T(CAR-T)细胞治疗复发难治性B细胞淋巴瘤患者疗效的因素,为进一步提高CAR-T疗效提供依据。2017年2月至2019年1月,从天津市第一中心医院血液科招募了34例复发难治性B细胞淋巴瘤患者。所有患者均接受CD19 CAR-T细胞治疗。对这些患者进行疗效、疗效不佳因素及不良反应评估。34例复发难治性B细胞淋巴瘤患者输注CD19 CAR-T细胞后,总缓解率为58.8%(20/34),完全缓解率为41.2%(14/34)。根据CAR-T细胞疗效,将患者分为两组,有效组20例,疗效不佳组14例。两组CD19 CAR-T细胞输注中位数分别为8.6(5.0-12.7)×10⁶/kg和9.7(5.8-15.0)×10⁶/kg,差异无统计学意义(0.654)。有效组和治疗不佳组CD19 CAR-T细胞百分比分别为10.28%(3.92%-44.16%)和4.05%(0.92%-28.63%)。有效组CAR-T细胞比例高于治疗不佳组,但差异无统计学意义(0.371)。巨大肿块的存在是影响CD19 CAR-T细胞疗效的不利因素,差异有统计学意义(0.001)。Logistic回归多因素分析显示,巨大肿瘤特征仍是CD19 CAR-T细胞疗效不佳的独立预后因素(0.005,0.039)。34例患者中,70.6%(24/34)在输注CD19 CAR-T细胞后出现不同程度不良反应,主要为细胞因子释放综合征(CRS)。发热中位发生时间为输注后第3天(0-11天)。16例为1级CRS,7例为2级,1例为3级。经糖皮质激素及支持治疗后均有改善。CD19 CAR-T细胞治疗在CD19(+)B细胞淋巴瘤中取得了一定疗效,但对部分患者疗效不佳。巨大肿块可能是CAR-T细胞治疗的不利因素。