Abstract
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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Acknowledgements
We would like to thank Manuela Salinero, Marta García-Blázquez and Manuel Delgado for their technical assistance, and Phil Mason for English language revision of the manuscript.
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DC and JL conceived the study; JL performed the statistical analysis; JL, LL-C and DC wrote the paper; JL, OL-G and RP-L collected the data and critically reviewed the paper; LL-C, LV, MC-C, MD-C, FS-G, EP-L, CG, IA, JAP-S and DC provided the patients and critically reviewed the paper; all authors approved the final version of the paper.
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Labrador, J., López-Corral, L., López-Godino, O. et al. Risk factors for thrombotic microangiopathy in allogeneic hematopoietic stem cell recipients receiving GVHD prophylaxis with tacrolimus plus MTX or sirolimus. Bone Marrow Transplant 49, 684–690 (2014). https://doi.org/10.1038/bmt.2014.17
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DOI: https://doi.org/10.1038/bmt.2014.17
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