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临床试验/NCT06582186
NCT06582186尚未招募4 期

Individualization of First Maintenance Doses of Voriconazole Using a Multiparametric Algorithm in Hematology Patients: a Prospective Single-arm Interventional Study

University Hospital, Grenoble1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年10月1日最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
Percentage of patients with initial plasma voriconazole trough concentration in the therapeutic range

研究概览

简要总结

The goal of this interventional single-arm study is to evaluate the interest of a multiparametric algorithm for individualization of first voriconazole maintenance doses for improvement of initial voriconazole exposure in adult patients with haematological malignancies. The main objective it aims is to determine the percentage of patients with initial voriconazole trough concentrations in the therapeutic range after individualization of first maintenance doses.

Participants will benefited from individualization of first voriconazole maintenance doses through a previously developed and validated multiparametric algorithm (publication in progress) taking into account CYP2C19 genotype, C reactive protein level and age.

详细描述

The currently recommended therapeutic drug monitoring of voriconazole has improved the efficacy of this treatment and reduced its adverse effects, especially for treatment and prophylaxis of invasive aspergillosis. However, dose adjustments made as part of this therapeutic drug monitoring only occur at the earliest 3 to 5 days after the initiation of treatment, whereas it is essential to achieve effective concentrations from the start of treatment. Simple a priori dose adjustment approaches based on CYP2C19 genotype have been shown to improve voriconazole exposure and treatment response. However other factors such as the patient's inflammatory status or age also influence voriconazole exposure, suggesting that strategies for individualizing initial voriconazole doses could be improved by integrating all covariates influencing voriconazole pharmacokinetics. In this line, a previous multicenter and international study has developped and validated an algorithm for calculating the first maintenance doses integrating not only the CYP2C19 genotype, but also the inflammatory status, the patient's age, and the presence (or not) of hematological malignancy. Here, the investigators propose to evaluate the interest of this multiparametric algorithm for improving initial exposure (within the first 4 days) to voriconazole in patients suffering from haematological malignancies.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • adult patient suffering from haematological malignancy
  • followed in the clinical hematology department or in the hematology day hospital of the Grenoble Alps University Hospital
  • consenting to carrying out CYP2C19 genotyping
  • likely to start treatment with voriconazole (for curative or prophylactic purposes as part of care)
  • having signed a written consent to participate
  • affiliated to a social security system

排除标准

  • comedication with strong inhibitors/inducers (valproic acid, phenytoin, carbamazepine, rifampicin)
  • Subject during exclusion period from another study,
  • Persons referred to in articles L1121-5 to L1121-8 of the CSP (corresponds to all protected persons: pregnant woman, parturient woman, breastfeeding mother, person deprived of liberty by judicial or administrative decision, persons subject to care psychiatric pursuant to articles L. 3212-1 and L. 3213-1 who do not fall under the provisions of article L. 1121-8, persons admitted to a health or social establishment for purposes other than research , minors, person subject to a legal protection measure or unable to express their consent)

结局指标

主要结局

Percentage of patients with initial plasma voriconazole trough concentration in the therapeutic range

时间窗: Day 5 +/-2

次要结局

  • Frequency of initial plasma voriconazole trough concentrations above the therapeutic range(Day 5 +/-2)
  • Frequency of initial plasma voriconazole trough concentrations below the therapeutic range(Day 5 +/-2)
  • Voriconazole area under the curve (AUC0-12h) after the first maintenance dose individualized(Day 2)
  • Time to get the therapeutic range(through study completion, an average of 3 months)
  • Treatment outcome in patients curatively treated(At month 3 +/- 15 days)
  • Frequency of side effects(through study completion, an average of 3 months)
  • Percentage of patients with initial plasma voriconazole trough concentration in the therapeutic range(Day 5 +/-2)

研究者

发起方
University Hospital, Grenoble
申办方类型
Other
责任方
Sponsor

研究点 (1)

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