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造血干细胞移植后死亡:随时间推移的变化、感染及相关因素。

Death after hematopoietic stem cell transplantation: changes over calendar year time, infections and associated factors.

机构信息

Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.

Policlinico G.B. Rossi, Verona, Italy.

出版信息

Bone Marrow Transplant. 2020 Jan;55(1):126-136. doi: 10.1038/s41409-019-0624-z. Epub 2019 Aug 27.

Abstract

Information on incidence, and factors associated with mortality is a prerequisite to improve outcome after hematopoietic stem cell transplantation (HSCT). Therefore, 55'668 deaths in 114'491 patients with HSCT (83.7% allogeneic) for leukemia were investigated in a landmark analysis for causes of death at day 30 (very early), day 100 (early), at 1 year (intermediate) and at 5 years (late). Mortality from all causes decreased from cohort 1 (1980-2001) to cohort 2 (2002-2015) in all post-transplant phases after autologous HSCT. After allogeneic HSCT, mortality from infections, GVHD, and toxicity decreased up to 1 year, increased at 5 years; deaths from relapse increased in all post-transplant phases. Infections of unknown origin were the main cause of infectious deaths. Lethal bacterial and fungal infections decreased from cohort 1 to cohort 2, not unknown or mixed infections. Infectious deaths were associated with patient-, disease-, donor type, stem cell source, center, and country- related factors. Their impact varied over the post-transplant phases. Transplant centres have successfully managed to reduce death after HSCT in the early and intermediate post-transplant phases, and have identified risk factors. Late post-transplant care could be improved by focus on groups at risk and better identification of infections of "unknown origin".

摘要

有关发病率和与死亡率相关的因素是改善造血干细胞移植(HSCT)后结局的前提。因此,在一项里程碑式分析中,对 114491 例接受 HSCT(83.7%为异基因)的白血病患者在第 30 天(极早期)、第 100 天(早期)、第 1 年(中期)和第 5 年(晚期)的死亡原因进行了调查。在自体 HSCT 后的所有移植后阶段,自队列 1(1980-2001 年)到队列 2(2002-2015 年),所有原因导致的死亡率均下降。异基因 HSCT 后,感染、GVHD 和毒性导致的死亡率在 1 年内下降,5 年内上升;移植后各阶段的复发死亡率均增加。不明原因的感染是感染性死亡的主要原因。从队列 1 到队列 2,致死性细菌和真菌感染减少,但不明原因或混合感染没有减少。感染性死亡与患者、疾病、供者类型、干细胞来源、中心和国家相关因素有关。它们的影响在移植后各阶段有所不同。移植中心成功地降低了 HSCT 后早期和中期的死亡率,并确定了风险因素。通过关注高危人群和更好地识别“不明原因”感染,可以改善晚期移植后的护理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d443/6957465/db0dc64e6614/41409_2019_624_Fig1_HTML.jpg

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