L. An, Ruifeng Hou, Huanhuan Guan, Zhihui Li, Tong Wu, Shuangyou Liu
{"title":"CD7 CAR-T therapy for an AML patient with CD7 expression","authors":"L. An, Ruifeng Hou, Huanhuan Guan, Zhihui Li, Tong Wu, Shuangyou Liu","doi":"10.15212/hod-2022-0007","DOIUrl":null,"url":null,"abstract":"To date, no ideal CAR-T product is available for treating acute myeloid leukemia (AML). Recently, CD7 CAR-T therapy has shown promising efficiency in treating T-cell acute lymphoblastic leukemia. Because the CD7 antigen is also expressed on the myeloid blasts of some patients with AML, it might serve as a target for immunotherapy in AML. Herein, we administered CD7-specific CAR-T cells into a 20-year-old woman with AML with CD7 expression. She had a history of multiple relapses (with extramedullary disease, EMD) and treatments (radiation and allogeneic hematopoietic cell transplantation). The most recent relapse indicated a high disease burden with multifocal EMD. After a combination regimen of azacytidine, venetoclax and ruxolitinib, she showed minimal residual disease-positive remission in the bone marrow (BM), and EMD remained present. Subsequently, donor-derived CD7 CAR-T cells infused at a dose of 5.5×105/kg completely eliminated all disease in the BM and extramedullary areas. Grade I cytokine release syndrome occurred with no neurotoxicity. CD7 CAR-T cells were detectable in the peripheral blood and BM. Fifty-five days after T-cell infusion, she underwent a second allogeneic hematopoietic cell transplantation and has survived in disease-free remission for more than 7 months.","PeriodicalId":107466,"journal":{"name":"Hematology and Oncology Discovery","volume":"45 1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hematology and Oncology Discovery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15212/hod-2022-0007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
To date, no ideal CAR-T product is available for treating acute myeloid leukemia (AML). Recently, CD7 CAR-T therapy has shown promising efficiency in treating T-cell acute lymphoblastic leukemia. Because the CD7 antigen is also expressed on the myeloid blasts of some patients with AML, it might serve as a target for immunotherapy in AML. Herein, we administered CD7-specific CAR-T cells into a 20-year-old woman with AML with CD7 expression. She had a history of multiple relapses (with extramedullary disease, EMD) and treatments (radiation and allogeneic hematopoietic cell transplantation). The most recent relapse indicated a high disease burden with multifocal EMD. After a combination regimen of azacytidine, venetoclax and ruxolitinib, she showed minimal residual disease-positive remission in the bone marrow (BM), and EMD remained present. Subsequently, donor-derived CD7 CAR-T cells infused at a dose of 5.5×105/kg completely eliminated all disease in the BM and extramedullary areas. Grade I cytokine release syndrome occurred with no neurotoxicity. CD7 CAR-T cells were detectable in the peripheral blood and BM. Fifty-five days after T-cell infusion, she underwent a second allogeneic hematopoietic cell transplantation and has survived in disease-free remission for more than 7 months.