| Literature DB >> 32658984 |
Hiroyuki Matsui1, Yasuyuki Arai1,2, Hiroharu Imoto3, Takaya Mitsuyoshi1,4, Naoki Tamura1, Tadakazu Kondo1, Junya Kanda1, Takayuki Ishikawa3, Kazunori Imada4, Yasunori Ueda5, Yusuke Toda1,6, Naoyuki Anzai7, Kazuhiro Yago8, Masaharu Nohgawa9, Akihito Yonezawa10, Hiroko Tsunemine11, Mitsuru Itoh12, Kazuyo Yamamoto13, Masaaki Tsuji14, Toshinori Moriguchi15, Akifumi Takaori-Kondo1.
Abstract
Transplant-associated thrombotic microangiopathy (TA-TMA) is a fatal complication of allogeneic hematopoietic stem cell transplantation (allo-HSCT). However, so far, no large cohort study determined the risk factors and the most effective therapeutic strategies for TA-TMA. Thus, the present study aimed to clarify these clinical aspects based on a large multicenter cohort. This retrospective cohort study was performed by the Kyoto Stem Cell Transplantation Group (KSCTG). A total of 2425 patients were enrolled from 14 institutions. All patients were aged ≥16 years, presented with hematological diseases, and received allo-HSCT after the year 2000. TA-TMA was observed in 121 patients (5.0%) on day 35 (median) and was clearly correlated with inferior overall survival (OS) (hazard ratio [HR], 4.93). Pre- and post-HSCT statistically significant risk factors identified by multivariate analyses included poorer performance status (HR, 1.69), HLA mismatch (HR, 2.17), acute graft-versus-host disease (aGVHD; grades 3-4) (HR, 4.02), Aspergillus infection (HR, 2.29), and veno-occlusive disease/sinusoidal obstruction syndrome (VOD/SOS; HR, 4.47). The response rate and OS significantly better with the continuation or careful reduction of calcineurin inhibitors (CNI) than the conventional treatment strategy of switching from CNI to corticosteroids (response rate, 64.7% vs 20.0%). In summary, we identified the risk factors and the most appropriate therapeutic strategies for TA-TMA. The described treatment strategy could improve the outcomes of patients with TA-TMA in the future.Entities:
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Year: 2020 PMID: 32658984 PMCID: PMC7362379 DOI: 10.1182/bloodadvances.2020002007
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529