Practice patterns and clinical outcomes of platelet alloimmunization in a comprehensive cancer center.

Abstract Background Platelet transfusion refractoriness (PTR) secondary to human leukocyte antigen (HLA) alloimmunization is a challenge in the treatment of hematology-oncologypatients and increases the risk of morbidity and mortality from bleeding events. Guidelines for treating PTR have not been clearly described in literature. We aim to describe the practice patterns for the management of PTR secondary to HLA alloimmunization, and to assess the mortality, thrombosis and bleeding-related clinical outcomes at 30 days from diagnosis. Methods A retrospective review of 51 cases of PTR secondary to HLA alloimmunization were analyzed. Results The majority of patients (98%) had a diagnosis of hematological malignancy of which 88.2% were undergoing active chemotherapy. Clinically relevant bleeding, by ISTH criteria, was observed in 33.3%; hemorrhagic shock was diagnosed in 7%. The rate of bleeding-related mortality was estimated at 7.8%. The use of antifibrinolytics and plasma products (including intravenous immunoglobulin) was more common in cases with major versus non-major bleeding. Grade A or B1U HLA matched products were available in less than half of cases. Conclusions There is heterogeneity in the management of the bleeding risk and bleeding events during PTR, with antifibrinolytics more commonly used in patients who suffered severe bleeding. Grade A and B1U HLA-matched platelets are not always readily available, and HLA-typing and HLA-antibody testing are not always performed prior to PTR. Prospective randomized control trials may help to determine the safety and efficacy of antifibrinolytics and other supportive measures in the management of PTR.