Phase II Study of Rituximab in Combination With Fludarabine and Cyclophosphamide for the Treatment of Relapsed Follicular Lymphoma
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 54
- 试验地点
- 18
- 主要终点
- Toxicity during the treatment period
研究概览
简要总结
Purpose of this study was to assess the safety profile and the anti-lymphoma activity of the FC+R combination.
详细描述
The natural history of follicular lymphomas is characterized by a high initial response rate to chemotherapy followed invariably by relapse, with subsequent remissions of progressively shorter duration. The majority of patients eventually die of their disease. As yet, there is no gold standard for the treatment of newly diagnosed or relapsed advanced FL.Rituximab(R) has been shown to be a highly effective agent in the treatment of FL, either alone or in combination with chemotherapy. The ability of R to sensitize indolent lymphoma derived cell lines to cytotoxic chemotherapy agents has been demonstrated. Furthermore, fludarabine (F) may also sensitize cells to the effects of R. Cyclophosphamide (C) and F have shown in vivo synergistic activity. In view of the single agent activity and demonstrated synergy between C and F, and between F and R, we evaluated FC+R in previously treated patients with advanced FL. The primary aim of this study was to assess the safety profile and clinical activity of the FC+R combination. The secondary goal was to evaluate the ability of the treatment to convert bone marrow Bcl2 positivity such that patients achieved molecular remissions.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 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 70 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •histologically documented WHO grade 1-2 ,CD20+,follicular lymphoma
- •relapsed Follicular lymphoma
- •stage III or IV disease
- •Stage II patients are eligible if they present with B symptoms or bulky disease
- •to have a need for therapy in the opinion of treating clinician
- •measurable disease
- •expected survival of 6 months or more
- •age 18 to 70 years
- •to have undergone < 3 lines of chemotherapy
- •performance status of 0 to 2
排除标准
- •known HIV infections
- •Known Hepatitis B or C
- •CNS lymphoma
- •previous malignancies, or cardiac, renal, hepatic, or respiratory failure
- •Pregnant or lactating women and patients of child bearing potential unless using birth control measures
结局指标
主要结局
Toxicity during the treatment period
Efficacy evaluated in terms of complete and partial response 1 month after the end of therapy
次要结局
- Efficacy evaluated in terms of molecular response ( bone marrow Bcl2 negativity after treatment)
