Risk factors for thrombotic microangiopathy in allogeneic hematopoietic stem cell recipients receiving GVHD prophylaxis with tacrolimus plus MTX or sirolimus

Transplantation-associated thrombotic microangiopathy (TA-TMA) is a feared complication of allogeneic hematopoietic SCT (HSCT) owing to its high mortality rate. The use of calcineurin inhibitors or sirolimus (SIR) for GVHD prophylaxis has been suggested as a potential risk factor. However, the impac...

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Published inBone marrow transplantation (Basingstoke) Vol. 49; no. 5; pp. 684 - 690
Main Authors LABRADOR, J, LOPEZ-CORRAL, L, ALBERCA, I, DEL CANIZO, M. C, PEREZ-SIMON, J. A, GONZALEZ-PORRAS, J. R, CABALLERO, D, LOPEZ-GODINO, O, VAZQUEZ, L, CABRERO-CALVO, M, PEREZ-LOPEZ, R, DIEZ-CAMPELO, M, SANCHEZ-GUIJO, F, PEREZ-LOPEZ, E, GUERRERO, C
Format Journal Article
LanguageEnglish
Published Basingstoke Nature Publishing Group 01.05.2014
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Summary:Transplantation-associated thrombotic microangiopathy (TA-TMA) is a feared complication of allogeneic hematopoietic SCT (HSCT) owing to its high mortality rate. The use of calcineurin inhibitors or sirolimus (SIR) for GVHD prophylaxis has been suggested as a potential risk factor. However, the impact of tacrolimus (TAC) and SIR combinations on the increased risk of TA-TMA is currently not well defined. We retrospectively analyzed the incidence of TA-TMA in 102 allogeneic HSCT recipients who consecutively received TAC plus SIR (TAC/SIR) (n=68) or plus MTX (TAC/MTX)±ATG (n=34) for GVHD prophylaxis. No significant differences were observed in the incidence of TA-TMA between patients receiving TAC/SIR vs TAC/MTX±ATG (7.4% vs 8.8%, P=0.8). Only grade III-IV acute GVHD, previous HSCT and serum levels of TAC >25 ng/mL were associated with a greater risk of TA-TMA. Patients developing TA-TMA have significantly poorer survival (P<0.001); however, TA-TMA ceased to be an independent prognostic factor when it was included in a multivariate model. In conclusion, the combination of TAC/SIR does not appear to pose a higher risk of TA-TMA. By contrast, we identified three different risk groups for developing TA-TMA.
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ISSN:0268-3369
1476-5365
DOI:10.1038/bmt.2014.17