Cao Yaqing, Lu Wenyi, Sun Rui, Jin Xin, Cheng Lin, He Xiaoyuan, Wang Luqiao, Yuan Ting, Lyu Cuicui, Zhao Mingfeng
The First Central Clinical College of Tianjin Medical University, Tianjin, China.
Department of Hematology, Tianjin First Central Hospital, Tianjin, China.
Front Oncol. 2019 Aug 19;9:767. doi: 10.3389/fonc.2019.00767. eCollection 2019.
Chimeric antigen receptor (CAR) T cells are emerging as a novel treatment for patients with refractory/relapsed B-cell non-Hodgkin lymphoma (B-NHL), and combination with PD1 inhibitors may further improve the efficacy of anti-CD19 CAR (CD19 CAR)-T cells in the treatment of lymphomas. In a single-center study, we evaluated the safety and efficacy of a combination therapy with CD19 CAR-T cells and an anti-PD-1 antibody (nivolumab) in patients with relapsed/refractory B-NHL. A total of 11 patients with refractory/relapsed B-NHL were recruited and subsequently received CD19 CAR-T cells and nivolumab. The primary end points were safety and feasibility. The infusions were safe, and no dose-limiting toxicities occurred. Grade 1 or 2 cytokine release syndrome (CRS) was observed in 25% (3/11) and 50% (6/11) of the patients, respectively, and only one patient (1/11) experienced neurotoxicity. The objective response rate (ORR) and complete response (CR) rate were 81.81% (9/11) and 45.45% (5/11), respectively. The median follow-up time was 6 (115) months. The median progression-free survival (PFS) time was 6 months (114 months), and 3 patients continued to have a response at the time of this writing. Our study demonstrated that the combination of CD19 CAR-T cells and nivolumab was feasible and safe and mediated potent anti-lymphoma activity, which should be examined further in prospective clinical trials in refractory/relapsed B-NHL.
嵌合抗原受体(CAR)T细胞正在成为难治性/复发性B细胞非霍奇金淋巴瘤(B-NHL)患者的一种新型治疗方法,与PD1抑制剂联合使用可能会进一步提高抗CD19 CAR(CD19 CAR)-T细胞治疗淋巴瘤的疗效。在一项单中心研究中,我们评估了CD19 CAR-T细胞与抗PD-1抗体(纳武单抗)联合治疗复发/难治性B-NHL患者的安全性和疗效。共招募了11例难治性/复发性B-NHL患者,随后接受了CD19 CAR-T细胞和纳武单抗治疗。主要终点是安全性和可行性。输注是安全的,未发生剂量限制性毒性。分别有25%(3/11)和50%(6/11)的患者观察到1级或2级细胞因子释放综合征(CRS),只有1例患者(1/11)出现神经毒性。客观缓解率(ORR)和完全缓解(CR)率分别为81.81%(9/11)和45.45%(5/11)。中位随访时间为6(115)个月。中位无进展生存期(PFS)为6个月(114个月),3例患者在撰写本文时仍有反应。我们的研究表明,CD19 CAR-T细胞与纳武单抗联合使用是可行且安全的,并介导了强大的抗淋巴瘤活性,这应在难治性/复发性B-NHL的前瞻性临床试验中进一步研究。