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

Authors :
Hoffmann, Christian
Schmid, Holger
Mueller, Markus
Teutsch, Christian
van Lunzen, Jan
Esser, Stefan
Wolf, Timo
Wyen, Christoph
Sabranski, Michael
Horst, Heinz-August
Reuter, Stefan
Vogel, Martin
Jaeger, Hans
Bogner, Johannes
Arasteh, Keikawus
Hoffmann, Christian
Schmid, Holger
Mueller, Markus
Teutsch, Christian
van Lunzen, Jan
Esser, Stefan
Wolf, Timo
Wyen, Christoph
Sabranski, Michael
Horst, Heinz-August
Reuter, Stefan
Vogel, Martin
Jaeger, Hans
Bogner, Johannes
Arasteh, Keikawus
Publication Year :
2011

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) was 6.2 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. (Blood. 2011;118(13):3499-3503)

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1252544467
Document Type :
Electronic Resource