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CD19嵌合抗原受体T细胞(CAR-T)治疗弥漫性大B细胞淋巴瘤或转化性滤泡性淋巴瘤后的血细胞减少:单中心经验

Cytopenias After CD19 Chimeric Antigen Receptor T-Cells (CAR-T) Therapy for Diffuse Large B-Cell Lymphomas or Transformed Follicular Lymphoma: A Single Institution Experience.

作者信息

Schaefer Andrew, Huang Ying, Kittai Adam, Maakaron Joseph E, Saygin Caner, Brammer Jonathan, Penza Sam, Saad Ayman, Jaglowski Samantha M, William Basem M

机构信息

Department of Medicine, University of Wisconsin, Madison, WI, USA.

Department of Internal Medicine, The Ohio State University, Columbus, OH, USA.

出版信息

Cancer Manag Res. 2021 Nov 30;13:8901-8906. doi: 10.2147/CMAR.S321202. eCollection 2021.

Abstract

INTRODUCTION

Patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL) have poor outcomes. Treatment with CD19 chimeric antigen receptor (CAR-T) cells, tisagenlecleucel and axicabtagene ciloleucel, has been associated with improved outcomes. Cytopenias were observed in clinical trials with both products; however, little is known regarding the patterns and outcomes of these cytopenias.

SUBJECTS AND METHODS

We reviewed DLBCL patients (=32) receiving either product between January and September 2018 at our institution.

RESULTS

Median duration of leukopenia, neutropenia, lymphopenia, anemia, and thrombocytopenia was 49, 9, 117.5, 125, and 95.5 days after CAR-T infusion, respectively. Filgrastim was used in 63% of patients, and 50% of patients received red cell or platelet transfusions. With the exception of neutropenia, increase in the duration of cytopenia of any lineage was associated with improvement in progression-free survival, and in overall survival in case of anemia. There was no association between the duration of cytopenias with either cytokine release syndrome or neurotoxicity.

DISCUSSION

Our data suggest a correlation between cytopenias and survival outcomes after CD19 CAR-T therapy. If validated, cytopenia may be proven useful as a biomarker of response and survival after CAR-T therapy.

摘要

引言

复发/难治性弥漫性大B细胞淋巴瘤(DLBCL)患者的预后较差。使用CD19嵌合抗原受体(CAR-T)细胞进行治疗,如tisagenlecleucel和axiabtagene ciloleucel,已显示出预后改善。在这两种产品的临床试验中均观察到血细胞减少;然而,对于这些血细胞减少的模式和结果知之甚少。

研究对象与方法

我们回顾了2018年1月至9月在我们机构接受这两种产品治疗的DLBCL患者(n=32)。

结果

CAR-T输注后,白细胞减少、中性粒细胞减少、淋巴细胞减少、贫血和血小板减少的中位持续时间分别为49天、9天、117.5天、125天和95.5天。63%的患者使用了非格司亭,50%的患者接受了红细胞或血小板输注。除中性粒细胞减少外,任何谱系血细胞减少持续时间的增加与无进展生存期的改善相关,对于贫血患者,与总生存期的改善相关。血细胞减少的持续时间与细胞因子释放综合征或神经毒性均无关联。

讨论

我们的数据表明CD19 CAR-T治疗后血细胞减少与生存结果之间存在相关性。如果得到验证,血细胞减少可能被证明是CAR-T治疗后反应和生存的有用生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0122/8643129/79b2bc4bf7c5/CMAR-13-8901-g0001.jpg

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