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首页> 外文期刊>Bone marrow transplantation >Pre-existing invasive fungal infection is not a contraindication for allogeneic HSCT for patients with hematologic malignancies: a CIBMTR study
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Pre-existing invasive fungal infection is not a contraindication for allogeneic HSCT for patients with hematologic malignancies: a CIBMTR study

机译:预先存在的侵袭性真菌感染对血液学恶性肿瘤患者的同种异体HSCT不是同种异体HSCT的禁忌症:CIBMTR研究

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摘要

Patients with prior invasive fungal infection (IFI) increasingly proceed to allogeneic hematopoietic cell transplantation (HSCT). However, little is known about the impact of prior IFI on survival. Patients with pre-transplant IFI (cases; n = 825) were compared with controls (n = 10247). A subset analysis assessed outcomes in leukemia patients pre-and post 2001. Cases were older with lower performance status (KPS), more advanced disease, higher likelihood of AML and having received cord blood, reduced intensity conditioning, mold-active fungal prophylaxis and more recently transplanted. Aspergillus spp. and Candida spp. were the most commonly identified pathogens. 68% of patients had primarily pulmonary involvement. Univariate and multivariable analysis demonstrated inferior PFS and overall survival (OS) for cases. At 2 years, cases had higher mortality and shorter PFS with significant increases in non-relapse mortality (NRM) but no difference in relapse. One year probability of post-HSCT IFI was 24% (cases) and 17% (control, P < 0.001). The predominant cause of death was underlying malignancy; infectious death was higher in cases (13% vs 9%). In the subset analysis, patients transplanted before 2001 had increased NRM with inferior OS and PFS compared with later cases. Pre-transplant IFI is associated with lower PFS and OS after allogeneic HSCT but significant survivorship was observed. Consequently, pre-transplant IFI should not be a contraindication to allogeneic HSCT in otherwise suitable candidates. Documented pre-transplant IFI is associated with lower PFS and OS after allogeneic HSCT. However, mortality post transplant is more influenced by advanced disease status than previous IFI. Pre-transplant IFI does not appear to be a contraindication to allogeneic HSCT.
机译:患有先前侵袭性真菌感染(IFI)的患者越来越多地进行同种异体造血细胞移植(HSCT)。然而,关于先前IFI对存活的影响很少。将移植前IFI(病例; N = 825)的患者与对照进行比较(n = 10247)。 2001年前和后期的白血病患者的次集分析评估结果。患者患者较低,性能状况下降,疾病更高,疾病较高,患有脐血,强度调节,模具活性真菌预防,更高的疾病最近移植。 aspergillus spp。和念珠菌spp。是最常见的病原体。 68%的患者主要是肺部受累。单变量和多变量分析表现出劣质的PFS和整体存活(OS)。在2年后,病例具有更高的死亡率和更短的PFS,非复发死亡率(NRM)显着增加,但复发没有差异。 HSCT IFI后的一年概率为24%(病例)和17%(对照,P <0.001)。死亡的主要原因是恶性肿瘤;病例中感染性死亡较高(13%vs 9%)。在子集分析中,与后期案例相比,2001年之前移植的患者在2001年之前的NRM增加了NRM和PFS。移植前的IFI与单相HSCT后与较低的PFS和OS相关联,但观察到显着的生存。因此,移植前的IFI不应该是对否则合适的候选者的同种式化合物HSCT的禁忌症。记录的预移植前IFI与异构HSCT后与较低的PFS和OS相关联。然而,死亡率后移植后的疾病状况的影响比以前的IFI更受影响。移植前的IFI似乎并不是同种异体HSCT的禁忌症。

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  • 来源
    《Bone marrow transplantation》 |2017年第2期|共9页
  • 作者单位

    Oregon Hlth &

    Sci Univ Adult Blood &

    Marrow Stem Cell Transplant Program Knight Canc Inst 3181;

    Med Coll Wisconsin Dept Med CIBMTR Milwaukee WI 53226 USA;

    Med Coll Wisconsin Dept Med CIBMTR Milwaukee WI 53226 USA;

    Oregon Hlth &

    Sci Univ Adult Blood &

    Marrow Stem Cell Transplant Program Knight Canc Inst 3181;

    Hosp Santa Creu &

    Sant Pau Div Clin Hematol Barcelona Spain;

    Univ Florida Dept Med Div Hematol &

    Oncol Gainesville FL USA;

    King Faisal Specialist Hosp Ctr &

    Res Dept Oncol Riyadh Saudi Arabia;

    NHLBI Hematol Branch Bethesda MD 20892 USA;

    Univ Calif San Francisco Dept Pediat Med Ctr San Francisco CA USA;

    Christian Med Coll &

    Hosp Dept Hematol Vellore Tamil Nadu India;

    Dana Farber Canc Inst Dept Pediat Oncol Boston MA 02115 USA;

    All Childrens Hosp Dept Hematol Oncol St Petersburg FL USA;

    Univ Hosp Case Med Ctr Seidman Canc Ctr Cleveland OH USA;

    Catholic Univ Korea Seoul St Marys Hosp BMT Ctr Seoul South Korea;

    Univ Rochester Med Ctr Dept Med Rochester NY 14642 USA;

    UMass Mem Med Ctr Dept Med Div Hematol &

    Oncol Worcester MA USA;

    Univ Cent Florida Coll Med Dept Internal Med Orlando FL 32816 USA;

    Vanderbilt Univ Med Ctr Dept Med Div Hematol Oncol Nashville TN USA;

    Univ Cincinnati Inst Canc Cincinnati OH USA;

    Oregon Hlth &

    Sci Univ Infect Dis Clin Portland OR 97201 USA;

    UC San Diego Hlth Infect Dis Program La Jolla CA USA;

    Univ Minnesota Med Ctr Div Hematol Oncol &

    Transplantat Dept Med Minneapolis MN 55455 USA;

    Fred Hutchinson Canc Res Ctr Vaccine &

    Infect Dis Div 1124 Columbia St Seattle WA 98104 USA;

    NCI Expt Transplantat &

    Immunol Branch NIH Bethesda MD 20892 USA;

    Univ Med Ctr Utrecht Pediat Blood &

    Marrow Transplantat Program Utrecht Netherlands;

    Nationwide Childrens Hosp Div Hematol Oncol Columbus OH USA;

    Univ North Carolina Chapel Hill Div Hematol Oncol Chapel Hill NC USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 治疗学;
  • 关键词

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