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Pure Red Cell Aplasia in Major ABO-Mismatched Allogeneic Hematopoietic Stem Cell Transplantation Is Associated with Severe Pancytopenia.
- Aung, Fleur;
- Lichtiger, Benjamin;
- Rondon, Gabriela;
- Yin, C;
- Alousi, Amin;
- Ahmed, Sairah;
- Andersson, Borje;
- Bashir, Qaiser;
- Ciurea, Stefan;
- Hosing, Chitra;
- Jones, Roy;
- Kebriaei, Partow;
- Khouri, Issa;
- Nieto, Yago;
- Oran, Betul;
- Parmar, Simrit;
- Qazilbash, Muzaffar;
- Shah, Nina;
- Shpall, Elizabeth;
- Champlin, Richard;
- Popat, Uday
- et al.
Published Web Location
https://doi.org/10.1016/j.bbmt.2016.02.008Abstract
In major ABO-mismatched allogeneic hematopoietic stem cell transplantation (HSCT) persistence of antidonor isohemagglutinins leads to pure red cell aplasia (PRCA). To investigate severe pancytopenia noted in a previous study of PRCA, we analyzed all major ABO-mismatched HSCT between January 2003 and December 2012. Of 83 PRCA patients, 13 (16%) had severe pancytopenia. Severe pancytopenia was defined as an absolute neutrophil count (ANC) < 1.5 K/μL or requiring granulocyte colony-stimulating factor, platelets < 50 K/μL or transfusion dependent, and PRCA with RBC transfusion dependence at post-transplant day 90. In 6 patients (46%) severe pancytopenia resolved after PRCA resolution. Two patients (15%) received a second transplant because of persistent pancytopenia/secondary graft failure, 1 (8%) died from secondary graft failure despite a stem cell boost, 1 (8%) did not recover his platelet counts despite RBC/ANC recovery, and 3 patients (23%) died from disease relapse. We found that severe pancytopenia is frequently associated with PRCA in 16% of major ABO-incompatible HSCT with a higher incidence in males and pancytopenia resolved with resolution of PRCA in 46% of patients.
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