4.6 Article

Multicentric Castleman's disease in HIV patients: a single-center cohort diagnosed from 2008 to 2018

Journal

INFECTION
Volume 49, Issue 5, Pages 945-951

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s15010-021-01618-5

Keywords

Castleman’ s disease; HHV-8; HIV; IL-6; Rituximab; Ruxolitinib

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This study involved nine male patients with HIV-associated MCD, all of whom were treated with Rituximab after diagnosis. Six patients achieved symptom resolution, with three also receiving tocilizumab. Other treatment options included splenectomy, valganciclovir, vincristine, siltuximab, and ruxolitinib. The relapse rate was 44% and the survival rate was 87.5% after one year and 71.4% after three years. The study concluded that rituximab remains the most effective therapy for MCD, while the efficacy of other treatments requires further confirmation in larger studies.
Purpose Castleman's disease (CD) is a well-established entity but there is a lack of available data regarding the management and therapy of HIV- and HHV-8-positive multicentric CD (MCD). We provide our own single-center experience with HIV-associated MCD. Methods We performed a retrospective, descriptive study on a cohort of patients with MCD, diagnosed and admitted to the infectious diseases or intensive care unit in the University Hospital Dusseldorf between 2008 and 2018. Included patients had a previous or new HIV diagnosis and clinical signs resembling MCD with evidence of HHV-8 replication or histological diagnosis for MCD. Results Nine male patients were included in the study. All patients were treated with Rituximab after diagnosis of MCD, with six of them acquiring resolution of symptoms. Three patients received tocilizumab additionally. Other treatment options included: splenectomy (2/9), valganciclovir (2/9), vincristine and siltuximab (1/9), ruxolitinib and Cytosorb(R) (2/9). The relapse rate was 44% (4/9) and the survival rate 87.5% after 1 year (8/9) and 71.4% after 3 years (5/7). Conclusion The most effective first-line therapy and retreatment option remains rituximab. The effectiveness of other treatment options like splenectomy or different immunotherapeutic approaches requires confirmation in larger-scale studies.

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