| Autor: |
Chellapandian, DeepakBabu, Das, Rupali, Zelley, Kristin, Wiener, Susan J., Zhao, Huaqing, Teachey, David T., Nichols, Kim E., Hale, Gregory, Minkov, Milen, Karlhuber, Susanne, Weinstein, Joanna L., Weitzman, Sheila, Moshous, Despina, Fischer, Alain, Jeng, Michael, Henry, Michael, Haupt, Riccardo, Svahn, Joanna, Zapotocka, Ester, Wolfson, Julie |
| Předmět: |
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| Zdroj: |
British Journal of Haematology; Aug2013, Vol. 162 Issue 3, p376-382, 7p, 1 Diagram, 2 Charts, 1 Graph |
| Abstrakt: |
Haemophagocytic lymphohistiocytosis ( HLH) is a life threatening complication of Epstein- Barr virus ( EBV) infection. The anti- CD20 antibody rituximab depletes B cells, leading to improved outcomes for patients with EBV-associated B-lymphoproliferative disorders. To gather data on the use of rituximab in EBV- HLH, we performed a retrospective investigation involving 42 EBV- HLH patients who had received treatment with rituximab-containing regimens. On average, patients received 3 rituximab infusions (range 1-10) at a median dose of 375 mg/m2. In all patients, rituximab was administered with other HLH-directed medications, including steroids, etoposide and/or ciclosporin. Rituximab-containing regimens appeared well tolerated and improved clinical status in 43% of patients. Examination of laboratory data obtained prior to and within 2-4 weeks after the first rituximab dose revealed significant reductions in EBV load (median load pre-rituximab: 114 200 copies/ml, median post-rituximab: 225 copies/ml, P = 0·0001) and serum ferritin levels (median ferritin pre-rituximab: 4260 μg/l, median post-rituximab: 1149 μg/l, P = 0·001). Thus, when combined with conventional HLH-directed therapies, rituximab improves symptoms, reduces viral load and diminishes inflammation. These data support the incorporation of rituximab into future prospective clinical trials for patients with EBV- HLH. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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