[t (17;19) (q21-22;p13)/TCF3-HLF 融合的 7 例急性 B 细胞淋巴细胞白血病的临床分析]。

Y Pu, Y Liu, X Y Zhou, B Q Song, J Zhang, W H Yan, Q Wang, J N Cen, H J Shen, Q R Wang, S N Chen, J L Pan, H Y Qiu
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引用次数: 0

摘要

本研究对苏州大学附属第一医院2017年6月至2022年8月收治的7例TCF3-HLF融合基因阳性急性B淋巴细胞白血病(B-ALL)患者的临床资料进行了回顾性分析,总结了他们的临床特征和预后。7名B-ALL患者中4男3女,中位年龄为18(11-33)岁。五名患者的CD33表达呈阳性,四名患者的核型正常。两名患者在初诊时出现高钙血症,一名患者在复发时出现高钙血症。六名患者在确诊时出现凝血功能障碍。经过诱导化疗后,七名患者中有五名获得了完全缓解,其中四名随后复发。两名患者在接受两轮诱导化疗后仍未获得缓解,其中一名患者在接受blinatumomab免疫疗法治疗后获得完全缓解。三名患者接受了嵌合抗原受体T细胞治疗,三名患者随后接受了造血干细胞移植。五名患者死亡,两名患者存活并获得持续完全缓解。TCF3-HLF阳性B-ALL非常罕见,复发率高,预后差。
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[Clinical analysis of 7 cases of acute B cell lymphoblastic leukemia with t (17;19) (q21-22;p13)/TCF3-HLF fusion].

A retrospective analysis of the clinical data of seven acute B-lymphoblastic leukemia (B-ALL) patients with TCF3-HLF fusion gene-positive admitted to the First Affiliated Hospital of Soochow University from June 2017 to August 2022 was conducted to summarize their clinical features and prognoses. The seven B-ALL patients comprised four males and three females, with a median age of 18 (11-33) years. Five patients tested positive for CD33 expression, and four patients had a normal karyotype. Two patients had hypercalcemia at the initial diagnosis, and one patient developed hypercalcemia at relapse. Six patients presented with coagulation dysfunction at diagnosis. After induction chemotherapy, five out of seven patients achieved complete remission, of which four subsequently relapsed. Two patients did not achieve remission even after two rounds of induction chemotherapy, with one achieving complete remission after treatment with blinatumomab immunotherapy. Three patients underwent chimeric antigen receptor T cell therapy, whereas three patients subsequently underwent hematopoietic stem cell transplantation. Five patients died, while two patients survived with sustained complete remission. TCF3-HLF-positive B-ALL is rare and has a high relapse rate and poor prognosis.

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