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Rituximab in the Treatment of HIV Associated Multicentric Castleman Disease Dependent on Chemotherapy

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

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00127569
Enrollment
25
Registered
2005-08-08
Start date
2003-05-31
Completion date
2006-01-31
Last updated
2007-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Giant Lymph Node Hyperplasia, HIV Infections

Keywords

HIV infections, Giant Lymph Node Hyperplasia, Herpesvirus 8, Human, Rituximab (Mabthera), Antibodies, Monoclonal

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.

Interventions

DRUGRituximab

Sponsors

Hoffmann-La Roche
CollaboratorINDUSTRY
French National Agency for Research on AIDS and Viral Hepatitis
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

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

Secondary

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026