Jin Xuelian, Liu Zhigang, Wu Yu, Ji Jie
Department of Hematology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Front Immunol. 2025 Jan 14;15:1475974. doi: 10.3389/fimmu.2024.1475974. eCollection 2024.
B-cell acute lymphoblastic leukemia (B-ALL) with the fusion gene has a poor prognosis, and the mortality rate exceeds 90%, particularly in cases of extramedullary relapse (EMR). Herein, we present a case of a 46-year-old male patient who developed relapsed B-ALL with . The patient initially achieved a complete remission (CR) after induction therapy and underwent haploidentical hematopoietic stem cell transplantation. Five months post-transplantation, he developed enlarged lymph nodes and subcutaneous masses. A lymph node biopsy confirmed EMR, without leukemia in the bone marrow or peripheral blood. The patient received the VCA regimen (venetoclax, chidamide, and azacitidine) and was regularly monitored through blood counts, marrow cell morphology analysis, flow cytometry, and computed tomography or positron emission tomography-computed tomography imaging. After the first VCA course, the patient achieved a second CR with only transient myelosuppression. Following two VCA courses, he received chimeric antigen receptor T-cell therapy, which led to complete metabolic remission and improved prognosis. This case underscores the potential of the VCA regimen as a bridging therapy for EMR in B-ALL with , although further studies are warranted.
具有该融合基因的B细胞急性淋巴细胞白血病(B-ALL)预后较差,死亡率超过90%,尤其是在髓外复发(EMR)的病例中。在此,我们报告一例46岁男性患者,其发生了伴有[此处原文缺失具体融合基因内容]的复发性B-ALL。该患者诱导治疗后最初达到完全缓解(CR),并接受了单倍体相合造血干细胞移植。移植后五个月,他出现了淋巴结肿大和皮下肿块。淋巴结活检证实为EMR,骨髓或外周血中无白血病。该患者接受了VCA方案(维奈克拉、西达本胺和阿扎胞苷)治疗,并通过血常规、骨髓细胞形态分析、流式细胞术以及计算机断层扫描或正电子发射断层扫描-计算机断层扫描成像进行定期监测。在第一个VCA疗程后,患者仅出现短暂的骨髓抑制,实现了第二次CR。在两个VCA疗程后,他接受了嵌合抗原受体T细胞疗法,实现了完全代谢缓解并改善了预后。该病例强调了VCA方案作为伴有[此处原文缺失具体融合基因内容]的B-ALL中EMR的桥接治疗的潜力,尽管仍需进一步研究。