| Literature DB >> 32124435 |
Narendranath Epperla1, Ang Li2, Brent Logan3,4, Caitrin Fretham5, Saurabh Chhabra3, Mahmoud Aljurf6, Lynette Chee7, Edward Copelan8, César O Freytes9, Peiman Hematti10, Hillard M Lazarus11, Mark Litzow12, Taiga Nishihori13, Richard F Olsson14,15, Tim Prestidge16, Wael Saber3, Baldeep Wirk17, Jean A Yared18, Alison Loren19, Marcelo Pasquini3.
Abstract
Transplant-associated thrombotic microangiopathy (TA-TMA) is a complication of allogeneic transplantation (allo-HCT). The incidence and risk factors associated with TA-TMA are not well known. A retrospective analysis from the Center for International Blood and Marrow Transplant Research (CIBMTR) was conducted including patients receiving allo-HCT between 2008 and 2016, with the primary objective of evaluating the incidence of TA-TMA. Secondary objectives included identification of risk factors associated with TA-TMA, and the impact of TA-TMA on overall survival and the need for renal replacement therapy (RRT). Among 23,665 allo-HCT recipients, the 3-year cumulative incidence of TA-TMA was 3%. Variables independently-associated with increased incidence of TA-TMA included female sex, prior autologous transplant, primary disease (acute lymphoblastic leukaemia and severe aplastic anaemia), donor type (mismatched or unrelated donor), conditioning intensity (myeloablative), GVHD prophylaxis (sirolimus + calcineurin inhibitor), pre-transplant kidney dysfunction and acute GVHD (time-varying effect). TA-TMA was associated with higher mortality (HR = 3·1, 95% Confidence Interval [CI] = 2·8-16·3) and RRT requirement (HR = 7·1, 95% CI = 5·7-311·6). This study provides epidemiologic data on TA-TMA and its impact on transplant outcomes. Increased awareness of the risk factors will enable providers to be vigilant of this uncommon but serious transplant complication. The results will also provide benchmarking for future study designs and comparisons.Entities:
Keywords: TA-TMA; allo-HCT; allogeneic transplantation; thrombotic microangiopathy
Mesh:
Year: 2020 PMID: 32124435 PMCID: PMC7726817 DOI: 10.1111/bjh.16457
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998