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Prepublished online as a Blood First Edition Paper on September 4, 2003; DOI 10.1182/blood-2003-03-0940.
Submitted March 28, 2003
Leukemia/BMT Program, British Columbia Cancer Agency, Vancouver, BC, Canada; Division of Hematology, Vancouver General Hospital, Vancouver, BC, Canada; Division of Hematology, University of British Columbia, Vancouver, BC, Canada * Corresponding author; email: dhogge{at}bccancer.bc.ca.
Randomized controlled trials (RCT) have shown a reduction in platelet alloimmunization and refractoriness in patients with acute leukemia (AL) with the use of post-storage leukoreduction of blood products. Universal pre-storage leukoreduction (ULR) of red cell and platelet products has been performed in Canada since August 1999. We conducted a retrospective analysis of 13,902 platelet transfusions in 617 patients undergoing chemotherapy (CT) for AL or stem cell transplantation (SCT) pre (n=315) and post (n=302) the introduction of ULR. Alloimmunization was significantly reduced (19 % to 7%, p< 0.001) in the post-ULR group. Alloimmune platelet refractoriness was similarly reduced (14% to 4%, p<0.001). Fewer patients in the post-ULR group received HLA-matched platelet (14% vs. 5%, p<0.001). Alloimmunization and alloimmune refractoriness in the 318 patients who were previously pregnant and/or transfused was also reduced post ULR (p=0.023 and p= 0.005 respectively). In a Cox regression model, the three independent factors that predicted for alloimmune refractoriness were non-leukoreduced blood products (RR [95% C.I] = 2.2 [1.2-4.3]), a history of pregnancy and/or transfusion (RR=2.3 [1.3-4.2]) and receipt of
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