【venetoclax联合酪氨酸激酶抑制剂和小剂量化疗治疗13例微小残留病阳性和复发/难治性Ph(+)急性淋巴细胞白血病的疗效和安全性】。

Q3 Medicine
H Ai, T T Liang, Q Wang, H F Wu, Q S Yin
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引用次数: 0

摘要

本研究旨在评估venetoclax (Ven)联合酪氨酸激酶抑制剂(TKI)和减少剂量化疗治疗微小残留病(MRD)阳性和复发/难治性(R/R) Ph阳性急性淋巴细胞白血病(Ph(+) ALL)患者的疗效和安全性。回顾性分析郑州大学附属肿瘤医院2015年7月至2024年2月收治的13例mrd阳性复发Ph(+) ALL患者的临床资料。该队列包括7名男性和6名女性,中位年龄为50岁(范围:37-71岁)。再诱导治疗由Ven和TKI联合小剂量化疗组成。13例患者中,mrd阳性10例,R/R病3例。在mrd阳性组中,9例(90%)达到完全分子缓解(CMR),中位缓解时间为47天(范围:30-80天);一名患者没有反应。在3例R/R患者中,2例(66.6%)达到完全缓解,1例无反应。整个队列的中位总生存期(OS)和无复发生存期(RFS)分别为21.5个月和7个月。在实现CMR的患者中,中位OS和RFS时间分别为35个月和34个月。5例患者发生≥3级血液学不良事件(38.4%);然而,所有病例的造血功能都恢复了,没有观察到≥3级感染或器官相关不良反应。这些研究结果表明,Ven联合TKI和小剂量化疗可能是MRD阳性和R/R Ph(+) ALL的有效和可耐受的治疗策略,特别是在显著提高MRD清除率方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[Efficacy and safety of venetoclax combined with tyrosine kinase inhibitors and reduced-dose chemotherapy in 13 cases of minimal residual disease-positive and relapsed/refractory Ph(+) acute lymphoblastic leukemia].

[Efficacy and safety of venetoclax combined with tyrosine kinase inhibitors and reduced-dose chemotherapy in 13 cases of minimal residual disease-positive and relapsed/refractory Ph(+) acute lymphoblastic leukemia].

This study sought to evaluate the efficacy and safety of venetoclax (Ven) in combination with tyrosine kinase inhibitors (TKI) and reduced-dose chemotherapy for the treatment of patients with minimal residual disease (MRD) -positive and relapsed/refractory (R/R) Ph-positive acute lymphoblastic leukemia (Ph(+) ALL). A retrospective analysis was conducted on the clinical data of 13 patients with MRD-positive and relapsed Ph(+) ALL admitted between July 2015 and February 2024 at the Affiliated Cancer Hospital of Zhengzhou University. The cohort included seven males and six females, with a median age of 50 years (range: 37-71 years). Reinduction therapy consisted of Ven and TKI administration combined with reduced-dose chemotherapy. Among the 13 patients, 10 were MRD-positive, and three had R/R disease. Of the MRD-positive group, nine (90%) achieved complete molecular response (CMR), with a median time to response of 47 days (range: 30-80) ; one patient did not respond. Among the three patients who had R/R, two (66.6%) achieved complete remission, while one patient was nonresponsive. The median overall survival (OS) and relapse-free survival (RFS) time for the entire cohort were 21.5 months and 7 months, respectively. In patients who achieved CMR, the median OS and RFS time were 35 months and 34 months, respectively. Grade ≥3 hematologic adverse events occurred in five patients (38.4%) ; however, hematopoietic function recovered in all cases, and no grade ≥3 infections or organ-related adverse reactions were observed. These findings suggest that Ven combined with TKI and reduced-dose chemotherapy may be an effective and tolerable therapeutic strategy for MRD-positive and R/R Ph(+) ALL, particularly in significantly improving MRD clearance rates.

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CiteScore
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