Schaefer Andrew, Huang Ying, Kittai Adam, Maakaron Joseph E, Saygin Caner, Brammer Jonathan, Penza Sam, Saad Ayman, Jaglowski Samantha M, William Basem M
Department of Medicine, University of Wisconsin, Madison, WI, USA.
Department of Internal Medicine, The Ohio State University, Columbus, OH, USA.
Cancer Manag Res. 2021 Nov 30;13:8901-8906. doi: 10.2147/CMAR.S321202. eCollection 2021.
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.
We reviewed DLBCL patients (=32) receiving either product between January and September 2018 at our institution.
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.
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.
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。
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)。
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。
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。