Risk factors and appropriate therapeutic strategies for thrombotic microangiopathy after allogeneic HSCT

Author:

Matsui Hiroyuki1,Arai Yasuyuki12ORCID,Imoto Hiroharu3,Mitsuyoshi Takaya14ORCID,Tamura Naoki1,Kondo Tadakazu1ORCID,Kanda Junya1ORCID,Ishikawa Takayuki3,Imada Kazunori4ORCID,Ueda Yasunori5,Toda Yusuke16,Anzai Naoyuki7,Yago Kazuhiro8,Nohgawa Masaharu9,Yonezawa Akihito10,Tsunemine Hiroko11,Itoh Mitsuru12,Yamamoto Kazuyo13,Tsuji Masaaki14,Moriguchi Toshinori15,Takaori-Kondo Akifumi1ORCID,

Affiliation:

1. Department of Hematology and Oncology and

2. Department of Clinical Laboratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan;

3. Department of Hematology, Kobe City Medical Center General Hospital, Hyogo, Japan;

4. Department of Hematology, Japanese Red Cross Osaka Hospital, Osaka, Japan;

5. Department of Hematology, Kurashiki Central Hospital, Okayama, Japan;

6. Department of Hematology, Tenri Hospital, Nara, Japan;

7. Department of Hematology, Takatsuki Red Cross Hospital, Osaka, Japan;

8. Department of Hematology, Shizuoka General Hospital, Shizuoka, Japan;

9. Deparment of Hematology, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan;

10. Department of Hematology, Kokura Memorial Hospital, Fukuoka, Japan;

11. Deparment of Hematology, Shinko Hospital, Hyogo, Japan;

12. Department of Hematology, Kyoto City Hospital, Kyoto, Japan;

13. Department of Hematology, Kitano Hospital, Osaka, Japan;

14. Department of Hematology, Japan Red Cross Otsu Hospital, Shiga, Japan; and

15. Department of Hematology, Kyoto-Katsura Hospital, Kyoto, Japan

Abstract

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.

Publisher

American Society of Hematology

Subject

Hematology

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