Etoposide-containing conditioning regimen reduces the occurrence of hemophagocytic lymphohistiocytosis after SCT

被引:30
作者
Kobayashi, R. [1 ]
Tanaka, J. [2 ]
Hashino, S. [2 ]
Ota, S. [3 ]
Torimoto, Y. [4 ]
Kakinoki, Y. [5 ]
Yamamoto, S. [6 ]
Kurosawa, M. [7 ]
Hatakeyama, N. [8 ]
Haseyama, Y. [9 ]
Sakai, H. [10 ]
Sato, K. [11 ]
Fukuhara, T. [12 ]
机构
[1] Sapporo Hokuyu Hosp, Dept Pediat, Sapporo, Hokkaido 0030006, Japan
[2] Hokkaido Univ Hosp, Stem Cell Transplantat Ctr, Sapporo, Hokkaido 060, Japan
[3] Sapporo Hokuyu Hosp, Dept Hematol, Sapporo, Hokkaido 0030006, Japan
[4] Asahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 078, Japan
[5] Asahikawa City Hosp, Dept Hematol, Asahikawa, Hokkaido, Japan
[6] Sapporo City Gen Hosp, Dept Hematol, Sapporo, Hokkaido, Japan
[7] Natl Hosp Org, Dept Hematol, Hokkaido Canc Ctr, Sapporo, Hokkaido, Japan
[8] Sapporo Med Coll, Dept Pediat, Sapporo, Hokkaido 060, Japan
[9] KKR Sapporo Med Ctr, Tonan Hosp, Dept Hematol, Sapporo, Hokkaido, Japan
[10] Teine Keijinkai Hosp, Dept Hematol, Sapporo, Hokkaido, Japan
[11] Hokkaido PWFAC Asahikawa Kosei Gen Hosp, Dept Hematol, Asahikawa, Hokkaido, Japan
[12] Hokkaido PWFAC Asahikawa Kosei Gen Hosp, Dept Palliat Care Med, Asahikawa, Hokkaido, Japan
基金
日本学术振兴会;
关键词
hemophagocytic lymphohistiocytosis; transplantation; etoposide; STEM-CELL TRANSPLANTATION; BONE-MARROW-TRANSPLANTATION; CORD BLOOD TRANSPLANTATION; GRAFT FAILURE; EARLY-ONSET; DIAGNOSIS;
D O I
10.1038/bmt.2013.145
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Hemophagocytic lymphohistiocytosis (HLH) is a rare life-threatening disease of severe hyperinflammation caused by uncontrolled proliferation of activated lymphocytes and macrophages that secrete high amounts of inflammatory cytokines. HLH occurring after SCT is difficult to diagnose. It is characterized by severe clinical manifestations and high mortality. Despite current therapeutic approaches, outcomes remain poor. We analyzed the incidence and risk factors of HLH after SCT and the response to treatment and prognosis of 554 patients with HLH after SCT. The cumulative incidence of HLH after SCT was 4.3% (24/554). Use of etoposide in the conditioning regimen was only factor that reduced HLH after SCT (P = 0.027). All patients who received autologous transplantation were successfully treated. Patients with liver dysfunction (for example, high total bilirubin level, prolonged prothrombin time and high level of fibrinogen degradation products) had a poor response to treatment for HLH. Physicians should be cautious of HLH, while not using etoposide for conditioning regimen.
引用
收藏
页码:254 / 257
页数:4
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