• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

伴有 CYP3A4 抑制剂的急性髓性白血病患者的血浆 Venetoclax 浓度。

Plasma Venetoclax Concentrations in Patients with Acute Myeloid Leukemia Treated with CYP3A4 Inhibitors.

机构信息

Department of Pharmaceutical Sciences, Tohoku University Hospital.

Faculty of Pharmaceutical Sciences, Tohoku University.

出版信息

Yakugaku Zasshi. 2024;144(7):775-779. doi: 10.1248/yakushi.24-00018.

DOI:10.1248/yakushi.24-00018
PMID:38945852
Abstract

Venetoclax (VEN) is used in patients with acute myeloid leukemia (AML) and is primarily metabolized by CYP3A4, a major drug-metabolizing enzyme. Patients with AML simultaneously administered VEN and CYP3A4 inhibitors require a more appropriate management of drug-drug interactions (DDIs). Here, we report two cases of patients with AML (54-year-old man and 22-year-old woman) administrated VEN and CYP3A4 inhibitors, such as posaconazole, cyclosporine, or danazol. In the first case, we evaluated the appropriateness of timing for adjusting VEN dosage subsequent to the cessation of posaconazole. Consequently, modifying the VEN dosage in conjunction with the cessation of Posaconazole simultaneously may result in elevated plasma VEN levels. In the second case, plasma VEN concentrations were markedly elevated when co-administered with several CYP3A4 inhibitors. Additionally, in vitro assays were conducted for reverse translational studies to analyze CYP3A4 inhibition. CYP3A4 inhibition by combinatorial administration of cyclosporine A and danazol was demonstrated in vitro, which potentially explains the increasing plasma VEN concentrations observed in clinical settings. Although the acquisition of therapeutic effects is a major priority for patients, frequent therapeutic drug monitoring and dosage adjustments considering DDIs would be important factors in chemotherapy.

摘要

维奈托克(VEN)用于治疗急性髓系白血病(AML),主要通过 CYP3A4 代谢,CYP3A4 是一种主要的药物代谢酶。同时给予 AML 患者 VEN 和 CYP3A4 抑制剂的患者需要更适当的药物相互作用(DDI)管理。在这里,我们报告了两例 AML 患者(54 岁男性和 22 岁女性)同时接受 VEN 和 CYP3A4 抑制剂,如泊沙康唑、环孢素或丹那唑的情况。在第一个病例中,我们评估了在停止泊沙康唑后调整 VEN 剂量的时间是否合适。因此,同时调整 VEN 剂量和停止泊沙康唑可能会导致血浆 VEN 水平升高。在第二个病例中,当与几种 CYP3A4 抑制剂联合给药时,血浆 VEN 浓度显著升高。此外,还进行了体外测定以进行反向转化研究来分析 CYP3A4 抑制。体外组合给予环孢素 A 和丹那唑可抑制 CYP3A4,这可能解释了在临床环境中观察到的血浆 VEN 浓度升高。尽管获得治疗效果是患者的主要关注点,但考虑到 DDI 的频繁治疗药物监测和剂量调整将是化疗的重要因素。

相似文献

1
Plasma Venetoclax Concentrations in Patients with Acute Myeloid Leukemia Treated with CYP3A4 Inhibitors.伴有 CYP3A4 抑制剂的急性髓性白血病患者的血浆 Venetoclax 浓度。
Yakugaku Zasshi. 2024;144(7):775-779. doi: 10.1248/yakushi.24-00018.
2
Dose adjustment of venetoclax when co-administered with posaconazole: clinical drug-drug interaction predictions using a PBPK approach.当与泊沙康唑同时给药时维奈托克的剂量调整:使用 PBPK 方法进行临床药物相互作用预测。
Cancer Chemother Pharmacol. 2021 Apr;87(4):465-474. doi: 10.1007/s00280-020-04179-w. Epub 2021 Jan 4.
3
Management of Venetoclax-Posaconazole Interaction in Acute Myeloid Leukemia Patients: Evaluation of Dose Adjustments.急性髓系白血病患者中维奈克拉与泊沙康唑相互作用的管理:剂量调整评估
Clin Ther. 2017 Feb;39(2):359-367. doi: 10.1016/j.clinthera.2017.01.003. Epub 2017 Feb 1.
4
Impact of ritonavir dose and schedule on CYP3A inhibition and venetoclax clinical pharmacokinetics.利托那韦剂量和给药方案对CYP3A抑制作用及维奈克拉临床药代动力学的影响。
Eur J Clin Pharmacol. 2018 Apr;74(4):413-421. doi: 10.1007/s00228-017-2403-3. Epub 2018 Jan 4.
5
Drug-drug interactions of newly approved small molecule inhibitors for acute myeloid leukemia.新型小分子抑制剂治疗急性髓系白血病的药物相互作用。
Ann Hematol. 2020 Sep;99(9):1989-2007. doi: 10.1007/s00277-020-04186-0. Epub 2020 Jul 18.
6
Development of Physiology Based Pharmacokinetic Model to Predict the Drug Interactions of Voriconazole and Venetoclax.基于生理学的药代动力学模型预测伏立康唑和维奈托克药物相互作用的研究进展。
Pharm Res. 2022 Aug;39(8):1921-1933. doi: 10.1007/s11095-022-03289-9. Epub 2022 Jun 21.
7
Clinical experience with the BCL2-inhibitor venetoclax in combination therapy for relapsed and refractory acute myeloid leukemia and related myeloid malignancies. Venetoclax 联合治疗复发/难治性急性髓系白血病及相关髓系恶性肿瘤的临床经验。
Am J Hematol. 2018 Mar;93(3):401-407. doi: 10.1002/ajh.25000. Epub 2017 Dec 23.
8
Physiologically based pharmacokinetic modeling and simulation to predict drug-drug interactions of ivosidenib with CYP3A perpetrators in patients with acute myeloid leukemia.基于生理学的药代动力学模型和模拟预测ivosidenib 与急性髓系白血病患者中 CYP3A 诱导剂的药物相互作用。
Cancer Chemother Pharmacol. 2020 Nov;86(5):619-632. doi: 10.1007/s00280-020-04148-3. Epub 2020 Sep 25.
9
characterization of acute myeloid leukemia patients undergoing hypomethylating agents and venetoclax regimen reveals a venetoclax-specific effect on non-suppressive regulatory T cells and PD-1TIM3 exhausted CD8 T cells.对接受低甲基化药物和 venetoclax 方案治疗的急性髓系白血病患者进行表征,揭示了 venetoclax 对非抑制性调节性 T 细胞和 PD-1TIM3 耗尽的 CD8 T 细胞的特异性作用。
Front Immunol. 2024 May 15;15:1386517. doi: 10.3389/fimmu.2024.1386517. eCollection 2024.
10
Single-center pediatric experience with venetoclax and azacitidine as treatment for myelodysplastic syndrome and acute myeloid leukemia.单中心儿科应用维奈托克联合阿扎胞苷治疗骨髓增生异常综合征和急性髓系白血病的经验。
Pediatr Blood Cancer. 2020 Oct;67(10):e28398. doi: 10.1002/pbc.28398. Epub 2020 Jul 31.

引用本文的文献

1
A New Histology-Based Prognostic Index for Acute Myeloid Leukemia: Preliminary Results for the "AML Urayasu Classification".一种基于组织学的急性髓系白血病新预后指数:“AML 浦安分类”的初步结果
J Clin Med. 2025 Mar 15;14(6):1989. doi: 10.3390/jcm14061989.
2
Final analysis of the phase 1b Chemotherapy and Venetoclax in Elderly Acute Myeloid Leukemia Trial (CAVEAT).老年急性髓系白血病化疗与维奈克拉试验(CAVEAT)1b期的最终分析。
Blood Adv. 2025 Apr 22;9(8):1827-1835. doi: 10.1182/bloodadvances.2024014900.
3
Relevance of plasma lenvatinib concentrations and endogenous urinary cytochrome P450 3A activity biomarkers in clinical practice.
血浆仑伐替尼浓度与内源性尿细胞色素 P4503A 活性生物标志物在临床实践中的相关性。
Pharmacol Res Perspect. 2024 Aug;12(4):e1241. doi: 10.1002/prp2.1241.