Improved outcome with rituximab in patients with HIV-associated multicentric Castleman disease

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Abstract

Although HIV-associated multicentric Castleman disease (HIV-MCD) is not classified as an AIDS-defining illness, mortality is high and progression to lymphoma occurs frequently. At present, there is no widely accepted recommendation for the treatment of HIV-MCD. In this retrospective (1998-2010), multicentric analysis of 52 histologically proven cases, outcome was analyzed with respect to the use of different MCD therapies and potential prognostic factors. After a mean follow-up of 2.26 years, 19 of 52 patients died. Median estimated overall survival (OS)was6.2 years. Potential risk factors, such as older age, previous AIDS, or lower CD4 T cells had no impact on OS. Treatment was heterogeneous, consisting of cytostatic and/or antiviral agents, rituximab, or combinations of these modalities. There were marked differences in the outcome when patients were grouped according to MCD treatment. Patients receiving rituximab-based regimens had higher complete remission rates than patients receiving chemotherapy only. The mean estimated OS in patients receiving rituximab alone or in combination with cytostatic agents was not reached, compared with 5.1 years (P ∇ .03). Clinical outcome and overall survival of HIV-MCD have markedly improved with rituximab-based therapies, considering rituximab-based therapies (with or without cytostatic agents) to be among the preferred first-line options in patients with HIV-MCD. © 2011 by The American Society of Hematology.

Figures

  • Table 1. Baseline characteristics at the time of HIV-MCD diagnosis (n 52)
  • Table 2. First- or second-line treatment for HIV-MCD
  • Figure 1. OS in patients with HIV-associated MCD.
  • Figure 2. OS in patients with HIV-associated MCD stratified according to MCD treatment. When patients receiving rituximab only (R Mono) or receiving R C were compared with patients receiving cytostatic therapy (with or without antiviral agents; C( V) only), there was a significant effect on OS toward rituximab-based regimens. The mean estimated OS of patients with R or R C was not reached, compared with 5.1 years (P .03) in patients receiving C( V).

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CITATION STYLE

APA

Hoffmann, C., Schmid, H., Müller, M., Teutsch, C., Van Lunzen, J., Esser, S., … Arasteh, K. (2011). Improved outcome with rituximab in patients with HIV-associated multicentric Castleman disease. Blood, 118(13), 3499–3503. https://doi.org/10.1182/blood-2011-02-333633

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