Rituximab in the Treatment of HIV Associated Multicentric Castleman Disease Dependent on Chemotherapy
Primary Purpose
HIV Infections, Giant Lymph Node Hyperplasia
Status
Terminated
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Rituximab
Sponsored by
About this trial
This is an interventional treatment trial for HIV Infections focused on measuring HIV infections, Giant Lymph Node Hyperplasia, Herpesvirus 8, Human, Rituximab (Mabthera), Antibodies, Monoclonal
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: Prior treatment with rituximab Evolutive lymphoma or Kaposi's sarcoma needing treatment Absence of effective contraception Pregnancy
Sites / Locations
Outcomes
Primary Outcome Measures
Sustained response rate of multicentric Castleman disease at day 60, after 4 infusions of rituximab
Secondary Outcome Measures
One-year disease-free survival
One-year event-free survival
Relapse rate at day 365
One-year lymphoma-free survival
Tolerance of rituximab
One-year overall survival
Change in HHV-8 viral load within one year
Change in lymphocyte B cell count within one year
Full Information
NCT ID
NCT00127569
First Posted
August 4, 2005
Last Updated
January 11, 2007
Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
Hoffmann-La Roche
1. Study Identification
Unique Protocol Identification Number
NCT00127569
Brief Title
Rituximab in the Treatment of HIV Associated Multicentric Castleman Disease Dependent on Chemotherapy
Official Title
Multicenter, Phase II Trial Assessing the Efficacy of Rituximab in HIV Infected Patients With Multicentric Castleman Disease Dependent on Chemotherapy (ANRS 117 Study, CastlemaB)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2007
Overall Recruitment Status
Terminated
Study Start Date
May 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2006 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
Hoffmann-La Roche
4. Oversight
5. Study Description
Brief Summary
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.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Giant Lymph Node Hyperplasia
Keywords
HIV infections, Giant Lymph Node Hyperplasia, Herpesvirus 8, Human, Rituximab (Mabthera), Antibodies, Monoclonal
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
25 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Rituximab
Primary Outcome Measure Information:
Title
Sustained response rate of multicentric Castleman disease at day 60, after 4 infusions of rituximab
Secondary Outcome Measure Information:
Title
One-year disease-free survival
Title
One-year event-free survival
Title
Relapse rate at day 365
Title
One-year lymphoma-free survival
Title
Tolerance of rituximab
Title
One-year overall survival
Title
Change in HHV-8 viral load within one year
Title
Change in lymphocyte B cell count within one year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
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
Exclusion Criteria:
Prior treatment with rituximab
Evolutive lymphoma or Kaposi's sarcoma needing treatment
Absence of effective contraception
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eric Oksenhendler, M.D.
Organizational Affiliation
AP-HP Hopital Saint-Louis
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Rituximab in the Treatment of HIV Associated Multicentric Castleman Disease Dependent on Chemotherapy
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