Reduced Chimeric Antigen Receptor T Cell Expansion Postinfusion Is Associated with Poor Survival in Patients with Large B Cell Lymphoma after Two or More Therapies.

IF 3.6 3区 医学 Q2 HEMATOLOGY Transplantation and Cellular Therapy Pub Date : 2025-01-06 DOI:10.1016/j.jtct.2025.01.001
Edward Abadir, Rebecca Wayte, Wenlong Li, Sachin Gupta, Shihong Yang, Elizabeth Reaiche, Katrina Debosz, Emily Anderson, James Favaloro, Esther Aklilu, Christina Brown, Christian Bryant, Scott Dunkley, Derek McCulloch, Stephen Larsen, John E J Rasko, Vinay Vanguru, P Joy Ho
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Abstract

CD19-directed chimeric antigen receptor T cell (CAR-T) therapy is now standard of care for relapsed/refractory large B cell non-Hodgkin lymphoma. Despite good overall response rates, many patients still experience disease progression and therefore it is important to predict those at risk of relapse following CAR-T therapy. We performed a prospective study using a flow cytometry assay at a single treatment center to assess early CAR T cell expansion in vivo 6 to 9 days after CAR T cell infusion. Early CAR T cell expansion was used in conjunction with additional clinical risk factors to identify those at greater risk of relapse or treatment failure. Forty-four patients treated with commercial CD19-directed CAR-T therapy were included in the study, with a median follow-up of 306 days. CAR T cell expansion of >30 cells/μL was associated with a lower risk of disease progression or death (hazard ratio, 0.34; P = .048), but did not correlate with the risk of death alone. Patients who had poor early CAR T cell expansion (<30 cells/μL) in addition to high lactate dehydrogenase (LDH) had significantly lower median progression-free survival and overall survival. High LDH level alone was not a statistically significant risk factor for death or disease progression, and thus the interaction between CAR T cell expansion and this clinical risk factor may be important in predicting response. The mean CAR T cell count was higher in patients with grade 2 to 4 cytokine release syndrome (CRS) compared to those with grade 0 to 1 CRS (54.9 cells/μL versus 25.5 cells/μL; P = .01). The methodology of this assay is easily reproducible outside of a clinical trial, allowing for real-life implementation in clinical settings. This study suggests that early assessment of CAR T cell expansion can assist in identifying patients with poor overall survival who may benefit from early intervention or more intensive monitoring.

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大B细胞淋巴瘤患者在两次或两次以上治疗后,输注后CAR - T扩增减少与生存率低相关。
CD19靶向嵌合抗原受体(CAR) t细胞疗法现在是复发/难治性大b细胞非霍奇金淋巴瘤的标准治疗方法。尽管总体反应率良好,但许多患者仍经历疾病进展,因此预测CAR - t细胞治疗后复发风险很重要。我们在单个治疗中心使用流式细胞术进行了一项前瞻性研究,以评估CAR- t细胞输注后6 - 9天体内早期CAR- t细胞的扩增情况。早期CAR - t细胞扩增与其他临床风险因素一起用于识别复发或治疗失败风险较高的患者。44名接受商业化CD19靶向CAR - t细胞治疗的患者被纳入研究,中位随访时间为306天。CAR - t细胞扩增量为bbb30个细胞/μl与疾病进展或死亡风险降低相关(HR 0.34, p=0.048),但与死亡风险无关。早期CAR - t细胞扩增不良的患者(
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来源期刊
CiteScore
7.00
自引率
15.60%
发文量
1061
审稿时长
51 days
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