search
Back to results

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
French National Agency for Research on AIDS and Viral Hepatitis
About
Eligibility
Locations
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    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
    search

    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

    We'll reach out to this number within 24 hrs