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淋巴细胞清除前绝对淋巴细胞计数对接受 CAR-T 细胞治疗的复发/难治性弥漫大 B 细胞淋巴瘤患者的预后价值

英文原题:Prognostic value of prelymphodepletion absolute lymphocyte counts in relapsed/refractory diffuse large B-cell lymphoma patients treated with chimeric antigen receptor T cells.

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Prognostic value of prelymphodepletion absolute lymphocyte counts in relapsed/refractory diffuse large B-cell lymphoma patients treated with chimeric antigen receptor T cells.

PubMed 2023/05/02(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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研究概要

数据提示,pre-LD ALC 可作为预测 CAR-T 细胞治疗 R/R DLBCL 患者结局的有用指标。

研究思路结论见上方概要

嵌合抗原受体(CAR)T细胞疗法近期取得了前所未有的疗效。然而,与应答和持久缓解相关的因素仍不明确。本研究旨在探讨淋巴细胞清除前(pre-LD)绝对淋巴细胞计数(ALC)对CAR-T 细胞治疗结局的影响。

我们进行了一项回顾性研究,纳入2016年3月1日至2021年12月31日在徐州医科大学附属医院接受CAR-T 细胞治疗的84例复发/难治性弥漫大B细胞淋巴瘤(R/R DLBCL)患者。根据pre-LD ALC的最佳截断值将入组患者分为高值组和低值组。采用Kaplan-Meier分析计算生存曲线。采用Cox比例风险模型进行单因素和多因素分析以评估预后因素。

ROC显示,pre-LD ALC的最佳截断值为1.05 x 10 9 /L。高pre-LD ALC患者的总体缓解(定义为部分缓解或完全缓解)率显著更高(75% versus 52.08%;P=0.032)。与高pre-LD ALC患者相比,低pre-LD ALC患者的总体生存(OS)和无进展生存期(PFS)显著更差(中位OS,9.6个月 versus 45.17个月 [P=0.008];中位PFS,4.07个月 versus 45.17个月 [P= 0.030])。同时,低pre-LD ALC是PFS和OS的独立危险因素。

展开英文摘要原文

We conducted a retrospective study of 84 patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL) who underwent CAR T cell treatment at the Affiliated Hospital of Xuzhou Medical University between March 1,2016 and December 31, 2021. The enrolled patients were divided into high group and low group according to the optimal cutoff value of pre-LD ALC. The Kaplan-Meier analyses was used to calculate survival curves. The Cox proportional hazards model was used for univariate and multivariate analysis to assess the prognostic factors.

The ROC showed that the optimal cutoff value of pre-LD ALC was 1.05 x 10 9 /L. The overall response (defined as partial response or complete response) rate was significantly higher in patients with a high pre-LD ALC (75% versus 52.08%; P=0.032). Patients with a low pre-LD ALC had significantly inferior overall survival (OS) and progression-free survival (PFS) compared with those having a high pre-LD ALC (median OS, 9.6 months versus 45.17 months [P=0.008]; median PFS, 4.07 months versus 45.17 months [P= 0.030]). Meanwhile, low pre-LD ALC is an independent risk factor for PFS and OS. DISCUSSION: The data suggested that pre-LD ALC may serve as a helpful indicator to predict the outcomes of CAR T cell therapy in patients with R/R DLBCL.

论文信息

作者
Lu Y、Zhu H、Liu Y、Wang Y、Sun Y、Cheng H、Yan Z、Cao J
单位
Blood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.China
文献类型
非美国政府资助研究
期刊
Frontiers in immunology2023
原文标识
PubMed 37205117 · DOI 10.3389/fimmu.2023.1155216