Ph-like acute lymphocytic leukemia:Clinical study of 9 cases and prognostic evaluation
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摘要: 目的:探讨Ph样急性淋巴细胞白血病(Ph-like ALL)的发病特点、治疗及预后。方法:采用荧光原位杂交检测9例Ph-like ALL患者常见基因重排,给予化疗联合芦可替尼、酪氨酸激酶抑制剂诱导治疗,未缓解的患者接受嵌合抗原受体T(CAR-T)细胞治疗,在获得完全缓解后行造血干细胞移植。其中6例受者接受异基因造血干细胞移植,1例受者接受自体造血干细胞移植。结果:9例患者中有7例进行了造血干细胞移植,其中6例受者移植后处于持续完全缓解,1例受者移植后早期复发。剩余2例未进行移植,其中1例在CAR-T治疗后本病复发死亡,另1例因重度感染死亡。结论:联合传统化疗、芦可替尼、酪氨酸激酶抑制剂和CAR-T等综合治疗手段使患者尽快达完全缓解,并序贯造血干细胞移植,有望改善此类患者的预后,未进行造血干细胞移植的此类患者预后较差。
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关键词:
- Ph样急性淋巴细胞白血病 /
- 造血干细胞移植 /
- 嵌合抗原受体T细胞
Abstract: Objective:To explore the clinical characteristics,treatment and prognosis of patients with Ph-like acute lymphocytic leukemia.Method:Fluorescent insitu hybridization was used to detect the rearrangement of susceptibility genes in 9 patients with Ph-like acute lymphocytic leukemia.Patients were treated with chemotherapy combined with ruxolitinib and tyrosine kinase inhibitor induction therapy.Patients without remission received chimeric antigen receptor T(CAR-T)cell therapy.After complete remission,hematopoietic stem cell transplantation was performed.Six patients received allogeneic hematopoietic stem cell transplantation and 1 patient received autologous hematopoietic stem cell transplantation.Result:Among the 9 patients,7 cases received hematopoietic stem cell transplantation,of which 6 cases achieved continuous complete remission and 1 case had early recurrence after transplantation.The remaining 2 cases did not receive transplantation,with one case dying from recurrence after CAR-T treatment and the other dying from severe infection.Conclusion:Combined therapy of chemotherapy,ruxolitinib,tyrosine kinase inhibitor and CAR-T are necessary for Ph-1 ike acute lymphocytic leukemia patients.Hematopoietic stem cell transplantation after an initial complete remission can improve the prognosis of patients.The prognosis of these patients without hematopoietic stem cell transplantation is poor. -
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