Clinical and laboratory correlates of platelet alloimmunization and refractoriness in the PLADO trial. Issue 3 (17th May 2016)

• Record Type: Journal Article
• Authors: Hess, J. R.; Trachtenberg, F. L.; Assmann, S. F.; Triulzi, D. J.; Kaufman, R. M.; Strauss, R. G.; Granger, S.; Slichter, S. J.
• Is Part Of: Vox sanguinis. Volume 111:Issue 3(2016)
• Page Start: 281
• Page End: 291
• Publication Date: 2016-05-17
• Subjects: clinicaltrials.gov number NCT00128713 -- prophylactic platelet transfusion -- response to platelet transfusion -- transfusion medicine hemostasis clinical trials network; Blood -- Periodicals; Blood -- Transfusion -- Periodicals; Immunohematology -- Periodicals; Immunopathology -- Periodicals; 615.39
• DOI: 10.1111/vox.12411
• Languages: English
• ISSNs: 0042-9007

Abstract

Abstract : Background and Objectives: Platelet alloimmunization and refractoriness to platelet transfusion are complications of platelet transfusion therapy. The platelet dose (PLADO) trial, as the largest prospective randomized trial of prophylactic platelet therapy to date, afforded an opportunity to analyse these two issues. Materials and Methods: PLADO patient records were examined for evidence of platelet alloimmunization, defined as an increase in HLA Class I panel‐reactive antibodies (PRA) to ≥20%, and clinical refractoriness, defined as two consecutive ≤4 h posttransfusion corrected platelet count increments (CCI) of <5000. Multivariate logistic regression, restricted to platelet‐transfused subjects who received exclusively either in‐process leucoreduction apheresis or whole blood‐derived (WBD) leucocyte‐reduced platelets, compared the frequency of these outcomes by platelet unit and patient characteristics. Results: Forty of 816 evaluable platelet‐transfused patients (5%) became alloimmunized during the trial. Prior pregnancy, chemotherapy only compared to progenitor cell transplant, and low platelet dose – all were associated with significantly higher rates of alloimmunization. Among 35 alloimmunized patients evaluated for refractoriness, 8 (23%) had two consecutive CCI < 5000/μl. Regardless of alloimmunization status, CCIs < 5000/μl were observed following 17% of platelet transfusions. Among 734 patients receiving at least two platelet transfusions, two consecutive CCIs of ≤5000 occurred in 102 (14%). Conclusions: The incidence of new platelet alloimmunization was low in the PLADO study, but follow‐up was at most 30 days. Alloimmunization was present in only 8 of 102 (8%) of observed cases of refractoriness, suggesting that other causes of poor posttransfusion increments are frequent.