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临床试验/NCT00393107
NCT00393107已完成2 期

Phase II Study of Rituximab in Combination With Fludarabine and Cyclophosphamide for the Treatment of Relapsed Follicular Lymphoma

Gruppo Italiano Studio Linfomi18 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2000年3月1日最近更新:
适应症
相关药物

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

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)

研究者

发起方
Gruppo Italiano Studio Linfomi
申办方类型
Other

研究点 (18)

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