Rituximab therapy for pure red cell aplasia due to anti-epoetin antibodies in a woman treated with epoetin-alfa: A case report

被引:8
作者
Behler C.M. [1 ,2 ]
Terrault N.A. [3 ]
Etzell J.E. [4 ]
Damon L.E. [1 ]
机构
[1] Department of Hematology and Oncology, University of California, San Francisco, CA
[2] Department of Hematology and Oncology, San Francisco Veterans Affairs Medical Center, San Francisco, CA
[3] Department of Gastroenterology, University of California, San Francisco, CA
[4] Department of Laboratory Medicine, University of California, San Francisco, CA
关键词
Chronic Kidney Disease; Reticulocyte Count; Nadir Absolute Neutrophil Count; Baseline White Blood Cell; Baseline White Blood Cell Count;
D O I
10.4076/1752-1947-3-7335
中图分类号
学科分类号
摘要
Introduction. Pure red cell aplasia due to anti-epoetin antibodies is a known complication of epoetin therapy for anemia due to chronic kidney disease. This disease has not previously been well described in the setting of therapy for chronic hepatitis C virus infection. While treatment for pure red cell aplasia due to anti-epoetin antibodies is usually with immunosuppressive therapy such as calcineurin inhibition, the safety of this treatment in chronic hepatitis C virus infection is unknown. To date, little has been published on the efficacy of rituximab on pure red cell aplasia due to anti-epoetin antibodies. Case presentation. This report describes a 65-year-old Asian-American woman who developed pure red cell aplasia from high titer neutralizing anti-epoetin antibodies after epoetin-alfa therapy during ribavirin and peg-interferon treatment for chronic hepatitis C virus infection. We describe the outcome of her treatment with rituximab. The reticulocyte count increased, and anti-epoetin antibody titer decreased with a loss of neutralizing activity in vitro, leading to a reduction in blood transfusions, and eventual resolution of anemia, without reactivation of hepatitis C virus. Conclusion. The diagnosis of pure red cell aplasia from anti-epoetin antibodies should be considered in patients undergoing therapy for chronic hepatitis C virus infection who develop severe anemia after administration of erythropoietin or darbepoetin. Though it is currently an off-label indication, rituximab is a therapeutic option for patients with pure red cell aplasia due to anti-epoetin antibodies. © 2009 licensee BioMed Central Ltd.
引用
收藏
相关论文
共 15 条
[1]  
Bennett C.L., Luminari S., Nissenson A.R., Tallman M.S., Klinge S.A., McWilliams N., McKoy J.M., Kim B., Lyons E.A., Trifilio S.M., Raisch D.W., Evens A.M., Kuzel T.M., Schumock G.T., Belknap S.M., Locatelli F., Rossert J., Casadevall N., Pure red-cell aplasia and epoetin therapy, N Engl J Med, 351, pp. 1403-1408, (2004)
[2]  
Cournoyer D., Toffelmire E.B., Wells G.A., Barber D.L., Barrett B.J., Delage R., Forrest D.L., Gagnon R.F., Harvey E.A., Laneuville P., Patterson B.J., Poon M.C., Posen G.A., Et al., Anti-erythropoietin antibody-mediated pure red cell aplasia after treatment with recombinant erythropoietin products: Recommendations for minimization of risk, J Am Soc Nephrol, 15, pp. 2728-2734, (2004)
[3]  
Boven K., Stryker S., Knight J., Thomas A., Van Regenmortel M., Kemeny D.M., Power D., Rossert J., Casadevall N., The increased incidence of pure red cell aplasia with an Eprex formulation in uncoated rubber stopper syringes, Kidney Int, 67, pp. 2346-2353, (2005)
[4]  
McKoy J.M., Stonecash R.E., Cournoyer D., Rossert J., Nissenson A.R., Raisch D.W., Casadevall N., Bennett C.L., Epoetin-associated pure red cell aplasia: Past, present, and future considerations, Transfusion, 48, pp. 1754-1762, (2008)
[5]  
Casadevall N., Cournoyer D., Marsh J., Messner H., Pallister C., Parker-Williams J., Rossert J., Recommendations on haematological criteria for the diagnosis of epoetin-induced pure red cell aplasia, Eur J Haematol, 73, pp. 389-396, (2004)
[6]  
Dieterich D.T., Wasserman R., Brau N., Hassanein T.I., Bini E.J., Bowers P.J., Sulkowski M.S., Once-weekly epoetin alfa improves anemia and facilitates maintenance of ribavirin dosing in hepatitis C virus-infected patients receiving ribavirin plus interferon alfa, Am J Gastroenterol, 98, pp. 2491-2499, (2003)
[7]  
Afdhal N.H., Dieterich D.T., Pockros P.J., Schiff E.R., Shiffman M.L., Sulkowski M.S., Wright T., Younossi Z., Goon B.L., Tang K.L., Et al., Epoetin alfa maintains ribavirin dose in HCV-infected patients: A prospective, double-blind, randomized controlled study, Gastroenterology, 126, pp. 1302-1311, (2004)
[8]  
Pockros P.J., Shiffman M.L., Schiff E.R., Sulkowski M.S., Younossi Z., Dieterich D.T., Wright T.L., Mody S.H., Tang K.L., Goon B.L., Bowers P.J., Leitz G., Afdhal N.H., Epoetin alfa improves quality of life in anemic HCV-infected patients receiving combination therapy, Hepatology, 40, 6, pp. 1450-1458, (2004)
[9]  
Stravitz R.T., Chung H., Sterling R.K., Luketic V.A., Sanyal A.J., Price A.S., Purrington A., Shiffman M.L., Antibody-mediated pure red cell aplasia due to epoetin alfa during antiviral therapy of chronic hepatitis C, Am J Gastroenterol, 100, pp. 1415-1419, (2005)
[10]  
Maloney D.G., Smith B., Applebaum F.R., The anti-tumor effect of monoclonal anti-CD20 antibody (mAb) therapy includes direct anti-proliferative activity and induction of apoptosis in CD20 positive non-Hodgkin's lymphoma (NHL) cell lines, Blood, 88, (1996)