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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Clinical features of hemophagocytic syndrome following BCMA CAR-T cell therapy in patients with relapsed/refractory multiple myeloma.
Clinical features of hemophagocytic syndrome following BCMA CAR-T cell therapy in patients with relapsed/refractory multiple myeloma.
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carHLH 在 BCMA CAR-T 细胞治疗患者中发生率较高,与治疗前骨髓肿瘤细胞百分比、CAR-T 细胞扩增及细胞因子分泌密切相关。基于 tocilizumab 和类固醇的用药可使 carHLH 患者获得可观的治疗效果。
分析复发/难治性多发性骨髓瘤患者接受B细胞成熟抗原(BCMA)嵌合抗原受体(CAR)T细胞治疗后发生噬血细胞综合征(HLH)的临床特征。:分析复发/难治性多发性骨髓瘤患者接受B细胞成熟抗原(BCMA)嵌合抗原受体(CAR)T细胞治疗后发生噬血细胞综合征(HLH)的临床特征。
2018年7月至2021年12月于浙江大学医学院附属第一医院接受BCMA CAR-T 细胞治疗(单中心期临床试验,ChiCTR1800017404)的99例复发/难治性多发性骨髓瘤患者(包括3例浆细胞白血病)纳入研究。分析这些患者的基线特征、实验室检查、治疗及临床反应。:2018年7月至2021年12月于浙江大学医学院附属第一医院接受BCMA CAR-T 细胞治疗(单中心期临床试验,ChiCTR1800017404)的99例复发/难治性多发性骨髓瘤患者(包括3例浆细胞白血病)纳入研究。分析这些患者的基线特征、实验室检查、治疗及临床反应。
CAR-T 细胞相关HLH(carHLH)发生于20例患者(20.20%),中位发生时间为细胞因子释放综合征(CRS)后7(0-19)d。carHLH患者主要为男性,表现为异常浆细胞比例高、重度CRS(3-4级)发生率更高,以及外周血中CAR-T 细胞强劲扩增(均P <0.05)。carHLH患者中白细胞介素(IL)-6、IL-10和干扰素(IFN)-水平、国际标准化比值和D-二聚体峰值升高,纤维蛋白原谷值降低(均P <0.01)。所有carHLH患者经适当干预后均缓解(包括7例使用tocilizumab,5例使用类固醇,6例两者均使用)。carHLH患者的客观缓解率略高于非carHLH患者[100.0%(17/17)vs. 94.87%(74/78),P >0.05]。CAR-T 细胞相关HLH(carHLH)发生于20例患者(20.20%),中位发生时间为细胞因子释放综合征(CRS)后7(0 19)d。carHLH患者主要为男性,表现为异常浆细胞比例高、重度CRS(3 4级)发生率更高,以及外周血中CAR-T 细胞强劲扩增(均P <0.05)。carHLH患者中白细胞介素(IL)-6、IL-10和干扰素(IFN)-水平、国际标准化比值和D-二聚体峰值升高,纤维蛋白原谷值降低(均P <0.01)。所有carHLH患者经适当干预后均缓解(包括7例使用tocilizumab,5例使用类固醇,6例两者均使用)。carHLH患者的客观缓解率略高于非carHLH患者[100.0%(17/17)vs. 94.87%(74/78),P >0.05]。结论:在接受BCMA CAR-T 细胞治疗的患者中,carHLH的发生率相对较高,其与治疗前骨髓中肿瘤细胞百分比、CAR-T 细胞的扩增及细胞因子的分泌密切相关。基于tocilizumab和类固醇的药物治疗可在carHLH患者中取得可观的治疗效果。
To analyze the clinical features of hemophagocytic syndrome (HLH) following B cell maturation antigen (BCMA) chimeric antigen receptor (CAR) T cell therapy in patients with relapsed/refractory multiple myeloma.
Ninety-nine patients with relapsed/refractory multiple myeloma (including 3 cases of plasma cell leukemia) undergoing BCMA CAR-T cell therapy (monocentric phase clinical trial, ChiCTR1800017404) in the First Affiliated Hospital, Zhejiang University School of Medicine from July 2018 to December 2021 were enrolled in the study. The baseline features, laboratory findings, treatment, and clinical response of these patients were analyzed.
CAR-T cell associated HLH (carHLH) occurred in 20 patients (20.20%), and the median onset time was 7(0-19) d after cytokine release syndrome (CRS). Patients with carHLH were maily male patients, and manifested as high percentage of abnormal plasma cells, higher incidence of severe CRS (grade 3-4), and robust expansion of CAR-T cells in the peripheral blood (all P <0.05). The levels of interleukin (IL)-6, IL-10 and interferon (IFN)- , the peak value of international normalized ratio and D-dimer were elevated, and the valley value of fibrinogen was decreased in patients with carHLH (all P <0.01). All carHLH patients resolved with proper intervention (including 7 cases with tocilizumab, 5 with steroids, 6 with both). The objective response rate in carHLH patients was slightly higher than that in non-carHLH patients [100.0% (17/17) vs. 94.87% (74/78), P >0.05].
The incidence of carHLH is relatively high in BCMA CAR-T cell treated patients, which is closely related to pretreatment tumor cell percentage in bone marrow, expansion of CAR-T cells and the secretion of cytokines. Medication based on tocilizumab and steroids can achieve considerable therapeutic effects in patient with carHLH.
: To analyze the clinical features of hemophagocytic syndrome (HLH) following B cell maturation antigen (BCMA) chimeric antigen receptor (CAR) T cell therapy in patients with relapsed/refractory multiple myeloma.
: Ninety-nine patients with relapsed/refractory multiple myeloma (including 3 cases of plasma cell leukemia) undergoing BCMA CAR-T cell therapy (monocentric phase clinical trial, ChiCTR1800017404) in the First Affiliated Hospital, Zhejiang University School of Medicine from July 2018 to December 2021 were enrolled in the study. The baseline features, laboratory findings, treatment, and clinical response of these patients were analyzed.
: CAR-T cell associated HLH (carHLH) occurred in 20 patients (20.20%), and the median onset time was 7(0 19) d after cytokine release syndrome (CRS). Patients with carHLH were maily male patients, and manifested as high percentage of abnormal plasma cells, higher incidence of severe CRS (grade 3 4), and robust expansion of CAR-T cells in the peripheral blood (all P <0.05). The levels of interleukin (IL)-6, IL-10 and interferon (IFN)- , the peak value of international normalized ratio and D-dimer were elevated, and the valley value of fibrinogen was decreased in patients with carHLH (all P <0.01). All carHLH patients resolved with proper intervention (including 7 cases with tocilizumab, 5 with steroids, 6 with both). The objective response rate in carHLH patients was slightly higher than that in non-carHLH patients [100.0% (17/17) vs. 94.87% (74/78), P >0.05].
: The incidence of carHLH is relatively high in BCMA CAR-T cell treated patients, which is closely related to pretreatment tumor cell percentage in bone marrow, expansion of CAR-T cells and the secretion of cytokines. Medication based on tocilizumab and steroids can achieve considerable therapeutic effects in patient with carHLH.
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