| Frontiers in Immunology | |
| Efficacy and safety of chimeric antigen receptor T cell therapy in relapsed/refractory diffuse large B-cell lymphoma with different HBV status: a retrospective study from a single center | |
| Immunology | |
| Xin Gao1  Rui Zou2  Zhengming Jin3  Changju Qu3  Danqing Kong3  Peng Wang3  Nana Ping3  Depei Wu3  | |
| [1] Department of Gastroenterology, The First Affiliated Hospital of Soochow University, Suzhou, China;National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, China;National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, China;Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Suzhou University, Suzhou, China; | |
| 关键词: diffuse large B cell lymphoma; hepatitis B virus; chimeric antigen receptor T cell therapy; HBV reactivation; cirrhosis; | |
| DOI : 10.3389/fimmu.2023.1200748 | |
| received in 2023-04-05, accepted in 2023-05-15, 发布年份 2023 | |
| 来源: Frontiers | |
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【 摘 要 】
BackgroundChimeric antigen receptor T cell (CAR-T) therapy is an effective salvage treatment in relapsed or refractory(r/r) diffuse large B-cell lymphoma (DLBCL), but the impact of hepatitis B virus (HBV) infection has not been studied.Methods and resultsHere, 51 patients with r/r DLBCL receiving CAR-T therapy were enrolled and analyzed at the First Affiliated Hospital of Soochow University. The overall response rate and the complete remission rate (CR) of CAR-T therapy were 74.5% and 39.2%, respectively. With a median follow-up of 21.1 months after CAR-T, the probabilities of overall survival (OS) and progression-free survival (PFS) at 36 months were 43.4% and 28.7%, respectively. These patients were divided into three cohorts including chronic HBV infection group (n=6), resolved HBV infection group (n=25) and non-HBV infection group (n=20). Bone marrow involvement was significantly higher in the HBV infection group(P<0.001), other basic characteristics before CAR-T therapy were comparable. Subgroup analysis showed that HBV infection status did not affect the efficacy of CAR-T therapy in CR rate, OS or PFS, and there was no significant difference in CAR-T related toxicities between three cohorts. Only one cirrhosis patient with chronic HBV infection experienced HBV reactivation.ConclusionsCAR-T therapy was effective and can be used safely in r/r DLBCL with HBV infection under proper monitoring and antiviral prophylaxis.
【 授权许可】
Unknown
Copyright © 2023 Kong, Ping, Gao, Zou, Wang, Wu, Jin and Qu
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202310109894518ZK.pdf | 1103KB |
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