NCT01788995已完成不适用
A Non-interventional Trial With Avastin as Front-line Treatment for Ovarian Cancer
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 63
- 试验地点
- 1
- 主要终点
- Treatment discontinuations/modifications
研究概览
简要总结
This non-interventional study will evaluate the routine use and the safety and efficacy of Avastin (bevacizumab) as first-line treatment in patients with advanced ovarian cancer (epithelial ovarian cancer, fallopian tube carcinoma, primary peritoneal carcinoma). Newly diagnosed patients who are initiated on carboplatin/paclitaxel chemotherapy in combination with Avastin will be followed for up to 15 months of treatment and 12 months of follow-up.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Adult patients, >/= 18 years of age
- •Patients with newly diagnosed advanced epithelial ovarian cancer (EOC), fallopian tube carcinoma (FTC) or primary peritoneal carcinomas (PPC) with indication for first-line carboplatin/paclitaxel chemotherapy in combination with Avastin
排除标准
- •Contraindications for Avastin according to the Summary of Product Characteristics
结局指标
主要结局
Treatment discontinuations/modifications
时间窗: approximately 4 years
Duration of treatment
时间窗: approximately 4 years
Clinical/demographic patient characteristics at initiation of treatment
时间窗: approximately 4 years
次要结局
- Progression-free survival(approximately 4 years)
- Safety: Incidence of adverse events(approximately 4 years)
研究者
研究点 (1)
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