Efficacy and safety of first-line rituximab in severe, acquired thrombotic thrombocytopenic purpura with a suboptimal response to plasma exchange. Experience of the French Thrombotic Microangiopathies Reference Center
- PMID: 21926591
- DOI: 10.1097/CCM.0b013e31822e9d66
Efficacy and safety of first-line rituximab in severe, acquired thrombotic thrombocytopenic purpura with a suboptimal response to plasma exchange. Experience of the French Thrombotic Microangiopathies Reference Center
Abstract
Objective: To assess the efficacy and safety of rituximab in adults responding poorly to standard treatment for severe autoimmune thrombotic thrombocytopenic purpura.
Design: Open-label prospective study. Outcomes in the survivors were compared to those of 53 historical survivors who were given therapeutic plasma exchange alone or with vincristine.
Setting: Hospitals belonging to the Reference Network for Thrombotic Microangiopathies in France.
Patients: Twenty-two adults with either no response or a disease exacerbation when treated with intensive therapeutic plasma exchange.
Intervention: Add-on rituximab therapy, four infusions over 15 days.
Measurements and main results: One patient died despite two rituximab infusions. In the rituximab-treated patients, the time to a durable remission was significantly shortened (p = .03), although the plasma volume required to achieve a durable remission was not significantly different compared to the controls. Platelet count recovery occurred within 35 days in all 21 survivors, compared to only 78% of the historical controls (p < .02). Of the rituximab-treated patients, none had a relapse within the first year but three relapsed later on. In patients treated with rituximab, a rapid and profound peripheral B-cell depletion was produced, lasting for 9 months and correlating with higher a disintegrin and metalloproteinase with thrombospondin-13 activity and lower anti-a disintegrin and metalloproteinase with thrombospondin-13 antibody titers. These differences were no longer significant after 12 months. No severe side effects occurred.
Conclusions: Adults with severe thrombocytopenic purpura who responded poorly to therapeutic plasma exchange and who were treated with rituximab had shorter overall treatment duration and reduced 1-yr relapses than historical controls.
Comment in
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Targeting B cells in severe thrombotic thrombocytopenic purpura--a road to cure?Crit Care Med. 2012 Jan;40(1):317-8. doi: 10.1097/CCM.0b013e318232d2b6. Crit Care Med. 2012. PMID: 22179358 Free PMC article. No abstract available.
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Thrombotic microangiopathy: rituximab in severe autoimmune TTP.Nat Rev Nephrol. 2012 Jan 31;8(3):131. doi: 10.1038/nrneph.2012.7. Nat Rev Nephrol. 2012. PMID: 22290542 No abstract available.
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Another beneficial effect of rituximab on refractory and relapsing thrombotic thrombocytopenic purpura: the role of interleukin-12 suppression?Crit Care Med. 2012 Apr;40(4):1391. doi: 10.1097/CCM.0b013e318241e3aa. Crit Care Med. 2012. PMID: 22425862 No abstract available.
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