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临床试验/NCT00127569
NCT00127569终止2 期

Multicenter, Phase II Trial Assessing the Efficacy of Rituximab in HIV Infected Patients With Multicentric Castleman Disease Dependent on Chemotherapy (ANRS 117 Study, CastlemaB)

French National Agency for Research on AIDS and Viral Hepatitis0 个研究点目标入组 25 人开始时间: 2003年5月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
终止
发起方
入组人数
25
主要终点
Sustained response rate of multicentric Castleman disease at day 60, after 4 infusions of rituximab

研究概览

简要总结

This trial is aimed to study the efficacy of 4 weekly cycles of rituximab in HIV-infected patients with multicentric Castleman disease (giant lymph node hyperplasia) dependent on chemotherapy. Efficacy is assessed by the complete response rate at day 60. The patients are followed until day 365.

详细描述

HIV-related multicentric Castleman disease (MCD) is a lymphoproliferative disorder characterized by lymphadenopathy with angiofollicular hyperplasia and plasma cell infiltration, associated with KSHV/HHV-8. Patients typically have systemic manifestations such as fever associated with lymphadenopathy, hepatosplenomegaly, respiratory symptoms, peripheral edema, cytopenia, hypergammaglobulinemia, hypoalbuminemia, and high levels of serum C reactive protein (CRP). Symptoms correlate with an important increase of KSHV/HHV-8 DNA in peripheral blood mononuclear cells. HIV-MCD is characterized by a rapidly progressive and often fatal course. HIV-MCD is often refractory to treatment. Vinca alkaloids produce frequent but short-lived responses, and most patients remain dependant upon chemotherapy.

Lymph nodes of patients with HIV-MCD specifically harbor the virus in B cells located in the mantle zone, which stain positively for the CD20 surface antigen. Rituximab, a humanized monoclonal anti-CD20 antibody, has been reported to be effective in some cases, with conflicting data in other cases. The optimal schedule of infusions remains unclear.

Kaposi's sarcoma is often associated with HIV-MCD, and the development of aggressive non-Hodgkin's lymphoma is not a rare outcome.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Confirmed multicentric Castleman disease, with dependence on vinblastine or VP16 for at least 3 months, whenever they have been splenectomized
  • •At least one Castleman crisis since onset of chemotherapy
  • •Ongoing highly active antiretroviral therapy (HAART) for at least 3 months
  • •No threshold of CD4 cell count and HIV-RNA
  • •Signed written informed consent

排除标准

  • •Prior treatment with rituximab
  • •Evolutive lymphoma or Kaposi's sarcoma needing treatment
  • •Absence of effective contraception
  • •Pregnancy

结局指标

主要结局

Sustained response rate of multicentric Castleman disease at day 60, after 4 infusions of rituximab

次要结局

  • One-year overall survival
  • One-year lymphoma-free survival
  • Tolerance of rituximab
  • One-year disease-free survival
  • One-year event-free survival
  • Relapse rate at day 365
  • Change in HHV-8 viral load within one year
  • Change in lymphocyte B cell count within one year

研究者

发起方
French National Agency for Research on AIDS and Viral Hepatitis
申办方类型
Other Gov

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