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低剂量维奈克拉联合抗真菌药物治疗急性髓系白血病的疗效与安全性:台湾一家医院的经验

Treatment outcomes and safety of reduced‑dose venetoclax plus antifungal agents to treat acute myeloid leukemia: A single hospital experience in Taiwan.

作者信息

Hsiao Sheng-Yen, Wu Kun-Yu, Huang Wen-Tsung, Lin Cheng-Yao, Chen Kuan-Yu, Weng Teng-Song

机构信息

Division of Hematology-Oncology, Department of Internal Medicine, Chi Mei Medical Center, Liouying, Tainan 736402, Taiwan, R.O.C.

Department of Nursing, Chung Hwa University of Medical Technology, Tainan 717302, Taiwan, R.O.C.

出版信息

Oncol Lett. 2025 Mar 21;29(5):241. doi: 10.3892/ol.2025.14987. eCollection 2025 May.

Abstract

Venetoclax, an orally administered B-cell lymphoma 2 inhibitor, requires dose adjustments when coadministered with cytochrome P450 inhibitors in patients with acute myeloid leukemia (AML). The present study retrospectively analyzed data on progression-free survival (PFS), overall survival (OS) and drug-related adverse events in patients with AML who received adjusted low-dose venetoclax with antifungal agents, compared with those receiving conventional chemotherapy regimens (I3A7, LDAC, and I2A5), at a single hospital. In total, 45 patients with AML who were treated between January 2015 and December 2021 were retrospectively included. A significantly longer median OS time was observed in the group receiving idarubicin [12 mg/m intravenous (IV) on days 1-3] and cytarabine (100 mg/m continuous IV infusion on days 1-7) (I3A7 group) (median not reached) compared with that in the venetoclax group [10.7 months; 95% confidence interval (CI), 6.3-20.8], the low-dose cytarabine (LDAC) group (4.7 months; 95% CI, 0.8-18.7) and the group receiving idarubicin (12 mg/m IV on days 1-2) with cytarabine (100 mg/m continuous IV infusion on days 1-5) (I2A5 group) (2.3 months; 95% CI, 0.5-2.3). Similarly, the median PFS time was significantly longer in the I3A7 group (29.0 months; 95% CI, 1.1-29.0) compared with that in the venetoclax (8.0 months; 95% CI, 0.8-10.8), LDAC (2.1 months; 95% CI, 0.1-6.4) and I2A5 (0.9 months; 95% CI, 0.1-4.7) groups. Grade 3 or higher adverse hematological events were common across all treatment groups. Cardiovascular events and grade 3 or higher tumor lysis syndrome occurred only in the venetoclax group (14 and 7%, respectively). In conclusion, low-dose venetoclax combined with antifungal agents appears to be less effective than standard treatment but superior to both LDAC and the I2A5 treatment regimens. Venetoclax also demonstrates a relatively low infection risk. However, careful monitoring for cardiovascular events and tumor lysis syndrome during venetoclax administration is crucial, particularly in patients with relevant medical histories.

摘要

维奈克拉是一种口服的B细胞淋巴瘤2抑制剂,在急性髓系白血病(AML)患者中与细胞色素P450抑制剂合用时需要调整剂量。本研究回顾性分析了在一家医院接受调整后的低剂量维奈克拉联合抗真菌药物治疗的AML患者与接受传统化疗方案(I3A7、小剂量阿糖胞苷和I2A5)的患者的无进展生存期(PFS)、总生存期(OS)及药物相关不良事件的数据。总共回顾性纳入了2015年1月至2021年12月期间接受治疗的45例AML患者。与维奈克拉组[10.7个月;95%置信区间(CI),6.3 - 20.8]、小剂量阿糖胞苷(LDAC)组(4.7个月;95% CI,0.8 - 18.7)和接受去甲氧柔红霉素(第1 - 2天静脉注射12 mg/m²)联合阿糖胞苷(第1 - 5天持续静脉输注100 mg/m²)的I2A5组(2.3个月;95% CI,0.5 - 2.3)相比,接受去甲氧柔红霉素(第1 - 3天静脉注射12 mg/m²)联合阿糖胞苷(第1 - 7天持续静脉输注100 mg/m²)的I3A7组观察到显著更长的中位OS时间(未达到中位值)。同样,I3A7组的中位PFS时间(29.0个月;95% CI,1.1 - 29.0)也显著长于维奈克拉组(8.0个月;95% CI,0.8 - 10.8)、LDAC组(2.1个月;95% CI,0.1 - 6.4)和I2A5组(0.9个月;95% CI,0.1 - 4.7)。3级或更高等级的血液学不良事件在所有治疗组中都很常见。心血管事件和3级或更高等级的肿瘤溶解综合征仅发生在维奈克拉组(分别为14%和7%)。总之,低剂量维奈克拉联合抗真菌药物似乎比标准治疗效果差,但优于LDAC和I2A5治疗方案。维奈克拉也显示出相对较低的感染风险。然而,在维奈克拉给药期间仔细监测心血管事件和肿瘤溶解综合征至关重要,尤其是在有相关病史的患者中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe3/12142305/5efa5666ff79/ol-29-05-14987-g00.jpg

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