Li Meng-Yun, Lin Zhi-Hong, Hu Ming-Ming, Kang Li-Qing, Wu Xiao-Xia, Chen Qi-Wei, Kong Xin, Zhang Jian, Qiu Hui-Ying, Wu De-Pei
Jiangsu Institute of Hematology, National Clinical Research Center for Hematologic Diseases, Collaborative Innovation Center of Hematology, The First Affiliated Hospital of Soochow University, Institute of Blood and Marrow Transplantation, Soochow University, 188 Shizi Street, Suzhou, 215006 P.R. China.
Suzhou Yongding Hospital, Suzhou, People's Republic of China.
Biomark Res. 2020 Aug 31;8:36. doi: 10.1186/s40364-020-00216-1. eCollection 2020.
Mixed phenotype acute leukemia (MPAL) is a rare leukemia and is regarded as a high-risk entity with a poor prognosis. Induction therapy of an acute lymphoblastic leukemia type or hybrid regimen and hematopoietic stem cell transplantation has been recommended for MPAL. However, the optimal therapies for relapsed or refractory MPAL remain unclear, especially for relapse after stem cell transplantation. Donor-derived chimeric antigen receptor T (CAR-T) cell therapy may be a promising therapeutic option for patients with MPAL who express target antigens and have relapsed after stem cell transplantation. However, recurrence remains a challenge, and reinfusion of CAR-T cells is not always effective. An infusion of secondary donor-derived humanized CD19-modified CAR-T cells may be effective in inducing remission.
We report a case of MPAL with CD19 expression. The patient was treated with acute lymphoblastic leukemia-like induction and consolidation therapies but remained positive for SET-NUP214 fusion gene transcript. He subsequently underwent a haploidentical stem cell transplantation but relapsed within 6 months. He then underwent donor-derived CD19-targeted CAR-T cell therapy and achieved a sustained, complete molecular remission. Unfortunately, he developed a CD19-positive relapse after 2 years. Donor-derived humanized CD19-directed CAR-T cells induced a second complete molecular remission without severe cytokine release syndrome or acute graft-versus-host disease.
This case demonstrated the efficacy and safety of humanized donor-derived CD19-modified CAR-T cell infusion for treating the recurrence of MPAL previously exposed to murine-derived CD19-directed CAR-T cells.
混合表型急性白血病(MPAL)是一种罕见的白血病,被视为预后不良的高危实体。对于MPAL,推荐采用急性淋巴细胞白血病类型的诱导治疗或混合方案以及造血干细胞移植。然而,复发或难治性MPAL的最佳治疗方法仍不明确,尤其是干细胞移植后的复发情况。供体来源的嵌合抗原受体T(CAR-T)细胞疗法对于表达靶抗原且干细胞移植后复发的MPAL患者可能是一种有前景的治疗选择。然而,复发仍然是一个挑战,CAR-T细胞再输注并不总是有效。输注二次供体来源的人源化CD19修饰的CAR-T细胞可能有效诱导缓解。
我们报告一例表达CD19的MPAL病例。该患者接受了类似急性淋巴细胞白血病的诱导和巩固治疗,但SET-NUP214融合基因转录本仍为阳性。他随后接受了单倍体相合干细胞移植,但在6个月内复发。然后他接受了供体来源的靶向CD19的CAR-T细胞治疗,并实现了持续的完全分子缓解。不幸的是,2年后他出现了CD19阳性复发。供体来源的人源化靶向CD19的CAR-T细胞诱导了第二次完全分子缓解,且未出现严重的细胞因子释放综合征或急性移植物抗宿主病。
本病例证明了人源化供体来源的CD19修饰的CAR-T细胞输注治疗先前接受鼠源靶向CD19的CAR-T细胞治疗后复发MPAL 的有效性和安全性。