Oral Voriconazole vs IV Low Dose Amphotericin B for Primary Antifungal Prophylaxis in Pediatric Acute Leukemia Induction:A Prospective, Randomized, Clinical Trial.
试验速览
- 阶段
- 3 期
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Prevention of possible, probable or proven fungal infection.
研究概览
简要总结
Hypothesis:Oral Voriconazole will be as effective as intravenous Amphotericin B as antifungal prophylaxis in induction of acute leukemia (ALL, AML) in pediatric patients, with less toxicity and more convenience.
详细描述
RATIONALE OF STUDY:
- In induction chemotherapy for childhood acute leukemia, our experience and international studies has shown that 30% of ALL and approximately 50% of AML patients require antifungal therapy. Mortality rates associated with documented fungal infection due to opportunistic yeasts and filamentous fungi have been high, ranging from 50-90% despite use of therapeutic amphotericin B or voriconazole.
- Currently licensed drug for use in pediatric patients are amphotericin B and its lipid derivatives; 5-flucytosine; azoles like fluconazole, itraconazole, voriconazole; and caspofungin.
- Limitation with Fluconazole- inactive against Aspergilosis, C. glabrata, C. krusei, C. parapsilosis and filamentous fungi.
- Limitation with Itraconazole- erratic oral absorption of capsule form, frequent drug interactions, non availability of oral suspension form for use in very small children who would not be able to take capsules.
- Amphotericin B and Voriconazole both have proven activity against filamentous fungi and candida species.
- There is no prospective, randomised trial comparing voriconazole and amphotericin B in prophylaxis of pediatric acute leukemia during induction.
Hence there is need to study their role in prophylaxis of this infection which has a high mortality despite therapy.
Study design: Prospective, Randomized, concealed, single institutional study.
Study population:
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- — 至 15 Years(Child)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients age </= 15 years with de novo acute leukemia (AML, ALL) undergoing induction chemotherapy.
- •No evidence of fungal infection at randomization
- •No pneumonia at presentation on CXR.
- •No systemic antifungal therapy within 7 days before randomization.
- •Febrile patients with no pneumonia, systemic fungal infection and hemodynamically stable will be eligible for study.
排除标准
- •Patients with baseline pneumonia on CXR.
- •Laboratory evidence of significant hepatic or renal dysfunction (defined as a SGOT or SGPT >5 times, Total bilirubin>2 times and Serum creatinine > 2 times upper limit of normal)
研究组 & 干预措施
1
Oral Voriconazole
干预措施: ORAL VORICONAZOLE and IV Amphotericin B (Drug)
2
IV Amphotericin B
干预措施: ORAL VORICONAZOLE and IV Amphotericin B (Drug)
结局指标
主要结局
Prevention of possible, probable or proven fungal infection.
时间窗: Completion of Induction Chemotherapy or successful recovery of ANC > 1000/mm3
次要结局
未报告次要终点
