[Ruxolitinib联合venetoclax和阿扎胞苷治疗JAK1、JAK3和STAT5B基因突变的难治性T-ALL患者:病例报告和文献综述】。]

Q3 Medicine
P P Xu, T Zhou, Y Y Xu, M X Peng, Y Du, T Xie, Y G Yang, J Ouyang, B Chen
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引用次数: 0

摘要

难治性急性T淋巴细胞白血病(T-ALL)对常规诱导治疗敏感性低、预后差,给治疗带来巨大挑战。本研究报告了南京大学鼓楼医院的一例JAK1、JAK3和STAT5B基因突变的难治性T-ALL患者。在标准VDLP方案化疗疗程失败后,患者接受了鲁索利替尼联合venetoclax和阿扎胞苷治疗。治疗后,患者骨髓极小残留病(MRD)阴性。值得注意的是,在同一阶段,胸腔灌注地塞米松联合依托泊苷后,胸腔积液和纵隔肿块明显改善。患者在获得骨髓缓解后还接受了异基因造血干细胞移植,并随访至2024年1月。Ruxolitinib联合venetoclax和氮杂胞苷治疗携带JAK1、JAK3和STAT5B突变的难治性T-ALL具有良好的疗效和安全性,为这类患者提供了一种新的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Ruxolitinib combined with venetoclax and azacitidine in the treatment of refractory T-ALL patients with JAK1, JAK3, and STAT5B gene mutations: a case report and literature review].

Refractory acute T-lymphoblastic leukemia (T-ALL), which is characterized by a low sensitivity to conventional induction therapy and poor prognosis, poses significant challenges during treatment. This study reported a case of refractory T-ALL patient with mutations in the JAK1, JAK3, and STAT5B genes from Nanjing University's Gulou Hospital. Following an unsuccessful course of standard VDLP regimen chemotherapy, the treatment was modified to include ruxolitinib in combination with venetoclax and azacitidine. Subsequent to this therapy, the patient achieved bone marrow minimal residual disease (MRD) negativity. Notably, pleural effusion and mediastinal mass significantly improved the post-chest cavity infusion of dexamethasone combined with etoposide at the same stage. The patient also underwent allogeneic hematopoietic stem cell transplantation upon achieving bone marrow remission and was followed up until January 2024. Ruxolitinib combined with venetoclax and azacytidine has shown promising efficacy and safety in treating refractory T-ALL harboring the JAK1, JAK3, and STAT5B mutations, providing a novel therapeutic approach for such patients.

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CiteScore
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