CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:CAR-T Cell Therapy Shows Similar Efficacy and Toxicity in Patients With DLBCL Regardless of CNS Involvement.
CAR-T Cell Therapy Shows Similar Efficacy and Toxicity in Patients With DLBCL Regardless of CNS Involvement.
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对于伴中枢神经系统(CNS)受累的复发/难治性弥漫大B细胞淋巴瘤(DLBCL),CAR-T(CAR-T)细胞疗法的疗效和毒性仍研究不足。本研究分析伴CNS受累的复发/难治性DLBCL患者接受CAR-T 治疗的结局,并与无CNS疾病患者比较。我们对接受CAR-T 治疗的复发/难治性DLBCL患者队列进行了单中心回顾性比较分析:CNS受累患者15例,无CNS受累患者65例。两队列的总体缓解率相当(均为80%;P=1.0),无进展生存期(P=0.157)和总生存期(P=0.393)亦相当。CNS组与非CNS组细胞因子释放综合征发生率相近,分别为93%和80%(P=1.0)。数值上,伴CNS表现患者的免疫效应细胞相关神经毒性综合征(所有级别)发生率较高(53%比29%;P=0.063),但未记录到4级事件。本研究提示,CAR-T 疗法对伴CNS表现的复发/难治性DLBCL患者有效且可行。
Efficacy and toxicity of chimeric antigen receptor T (CAR-T) cell therapy in relapsed/refractory (r/r) diffuse large B-cell lymphoma (DLBCL) with central nervous system (CNS) involvement remain understudied.
Here we analyzed the outcomes of CAR-T cell therapy in r/r DLBCL patients with CNS involvement and compared them with patients without CNS disease. Retrospective and monocentric comparative analysis of patient cohort with r/r DLBCL treated with CAR-T cell therapy: 15 patients with CNS versus 65 patients without CNS involvement.
Overall response rates (80% versus 80%; P = 1. 0), progression-free survival ( P = 0. 157), and overall survival ( P = 0. 393) were comparable for both cohorts. The frequency of cytokine release syndrome was comparable in the CNS and non-CNS cohorts; 93% versus 80%; P = 1. 0. Numerically, immune effector-cell-associated neurotoxicity syndrome (all grades) was more frequent in patients with CNS manifestation (53% versus 29%; P = 0. 063), although no grade 4 events were documented.
Our study suggests that CAR-T cell therapy is effective and feasible in patients with r/r DLBCL and CNS manifestation.
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