通过癌症患者的血度进行埃弗罗利斯:前性的纵向观察多中心研究 (DIANA-1项目)
Eduard Fort-Casamartina1, Sonia Pernas2, Sara Otero1
1Pharmacy Department, Institut Català Oncologia (ICO), Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), L'Hospitalet Llobregat, 08908 Barcelona, Spain.
Journal of clinical medicine
|January 11, 2025
概括
许多接受everolimus治疗的癌症患者可能无法达到最佳药物水平,因此需要治疗药物监测 (TDM). 这项研究调查了超出范围的恒胺度的患病率及其在瘤学环境中的影响因素.
科学领域:
- 在瘤学瘤学.
- 药理学 药理学是指药理学的学科.
- 翻译医学是一种翻译医学.
背景情况:
- 作为mTOR抑制剂的Everolimus可以治疗各种癌症,但具有显著的药理动力学变异性.
- 在瘤学中常规治疗药物监测 (TDM) 对于everolimus不是标准的做法.
- 了解药物度变化对于优化癌症治疗至关重要.
研究的目的:
- 为了确定超出治疗范围 (10-26.3 ng/mL) 的埃弗罗利斯最低稳定状态度 (Cminss) 的流行率.
- 探索非治疗性恒大水平与患者/治疗特定因素之间的相关性.
- 为癌症治疗中个性化剂量策略提供见解.
主要方法:
- 多中心,前性观察队列研究.
- 包括60名患有转移性乳腺癌,神经内分泌癌或癌的患者,接受Everolimus治疗.
- 定期采取血液样本 (每4-6周一次) 用于Cminss监测和与临床数据的相关性分析.
主要成果:
- 假设30-50%的患者将有超出目标治疗范围的Everolimus水平.
- 旨在确定与可变药物度相关的人口,临床,实验室和遗传因素.
- 将量化在现实世界瘤学环境中低于最佳的常利暴露的发生率.
结论:
- 这些发现可能有助于在癌症治疗中实施常规的EverolimusTDM.
- 结果可以为个性化剂量策略提供信息,以提高治疗疗效和安全性.
- 有助于优化Everolimus治疗和潜在的其他向抗癌药物.
更多相关视频
06:00Development of a Human Preclinical Model of Osteoclastogenesis from Peripheral Blood Monocytes Co-cultured with Breast Cancer Cell Lines
Published on: September 13, 2017
7.1K
09:44Pretargeted Radioimmunotherapy Based on the Inverse Electron Demand Diels-Alder Reaction
Published on: January 29, 2019
10.0K
相关概念视频
Drug Concentration Versus Time Correlation
608
The plasma drug concentration-time curve is a crucial tool in pharmacokinetics, representing the drug's concentration in plasma at different time intervals post-administration. This curve illustrates the drug's journey from absorption into the systemic circulation, distribution to body tissues, and eventual elimination through excretion or biotransformation.
Two pivotal parameters are the minimum effective concentration (MEC) and the minimum toxic concentration (MTC). The MEC is the...
Two pivotal parameters are the minimum effective concentration (MEC) and the minimum toxic concentration (MTC). The MEC is the...
608
Drug Concentrations: Measurements
319
Drug concentration is the quantity of a drug present in a biological sample. Measuring drug amounts in biological samples allows the clinician to understand how a drug is absorbed, distributed, metabolized, and excreted. Samples can be obtained through invasive or non-invasive methods. Invasive techniques involve surgical or parenteral interventions to gather blood, cerebrospinal fluid, or tissue biopsy. Conversely, non-invasive approaches provide samples like urine, feces, and saliva.
Plasma...
Plasma...
319
