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首页> 外文期刊>Bone marrow transplantation >Predictors of hematologic malignancy relapse in patients with advanced chronic graft-versus-host disease
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Predictors of hematologic malignancy relapse in patients with advanced chronic graft-versus-host disease

机译:先进慢性移植患者血液学恶性复发预测因素患者患者

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摘要

Malignancy relapse remains a major barrier to treatment success in patients after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Chronic graft-versus-host disease (cGVHD) markedly reduces hematologic malignancy relapse risk, but relapses still occur in these patients. Patients (n = 275) with moderate or severe cGVHD were enrolled on the National Cancer Institute (NCI) prospective cross-sectional natural history study (NCT00092235). Subjects were median 36 months after allo-HSCT and were followed subsequently for malignancy relapse and survival. Seventeen patients experienced relapse. In a multivariable model including time-dependent influences on relapse, risk factors associated with increased risk of relapse included shorter time from transplant to cGVHD evaluation (HR 0.279, 95% CI 0.078-0.995) and lower number of prior lines of systemic immunosuppressive therapy for cGVHD (HR 0.260, 95% CI 0.094-0.719). In a model excluding time-dependent influences on relapse risk, lower number of prior lines of systemic immunosuppressive therapy for cGVHD (HR 0.288, 95% CI 0.103-0.804), lower C4 complement level (HR 0.346, 95% CI 0.129-0.923), and higher body mass index (HR 3.222, 95% CI 1.156-8.974), were all associated with increased relapse risk. Parameters indicating cGVHD severity and activity are associated with risk of malignancy relapse. Classical predictors of relapse after allo-HSCT do not seem to be prognostic.
机译:恶性复发仍然是同种异体造血干细胞移植(Allo-HSCT)后患者治疗成功的主要障碍。慢性接枝与宿主疾病(CGVHD)显着降低血液学恶性复发风险,但这些患者仍然发生复发。患者(n = 275)中度或严重的CGVHD均注册了国家癌症研究所(NCI)预期横截面自然历史研究(NCT00092235)。受试者在allo-hsct后36个月中位,随后遵循恶性复发和生存。十七名患者经历过复发。在多变量模型,包括对复发的时间依赖性影响,与移植风险增加的风险因素包括从移植到CGVHD评估的时间较短(HR 0.279,95%CI 0.078-0.995)和较少数量的全身免疫抑制治疗CGVHD(HR 0.260,95%CI 0.094-0.719)。在不包括复发风险的时间依赖性影响的模型中,对CGVHD的全身免疫抑制治疗的现有线数量减少(HR 0.288,95%CI 0.103-0.804),降低C4补体水平(HR 0.346,95%CI 0.129-0.923)和更高的体重指数(HR 3.222,95%CI 1.156-8.974)均与复发风险增加有关。指示CGVHD严重程度和活动的参数与恶性复发的风险相关。 allo-hsct后复发的古典预测因子似乎并不是预后。

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  • 来源
    《Bone marrow transplantation》 |2021年第7期|共9页
  • 作者单位

    NCI Immune Deficiency Cellular Therapy Program Ctr Canc Res NIH 9000 Rockville Pike Bldg 10;

    NCI Immune Deficiency Cellular Therapy Program Ctr Canc Res NIH 9000 Rockville Pike Bldg 10;

    NCI Biostat &

    Data Management Sect NIH 9609 Med Ctr Dr Room 2W334 Bethesda MD 20850 USA;

    NCI Immune Deficiency Cellular Therapy Program Ctr Canc Res NIH 9000 Rockville Pike Bldg 10;

    NCI Immune Deficiency Cellular Therapy Program Ctr Canc Res NIH 9000 Rockville Pike Bldg 10;

    NCI Immune Deficiency Cellular Therapy Program Ctr Canc Res NIH 9000 Rockville Pike Bldg 10;

    NCI Immune Deficiency Cellular Therapy Program Ctr Canc Res NIH 9000 Rockville Pike Bldg 10;

    NCI Outcomes Res Branch Div Canc Control &

    Populat Sci NIH Bethesda MD 20892 USA;

    NCI Immune Deficiency Cellular Therapy Program Ctr Canc Res NIH 9000 Rockville Pike Bldg 10;

    NIAMSD Dermatol Branch NIH 9000 Rockville Pike Bldg 10 Room 12N240A Bethesda MD 20892 USA;

    NIH Pain &

    Palliat Care Serv Ctr Clin 10 Ctr Dr Bethesda MD 20892 USA;

    NIH Dept Rehabil Med Ctr Clin 10 Ctr Dr Bethesda MD 20892 USA;

    NEI NIH 31 Ctr Dr Bldg 31 MSC 2510 Bethesda MD 20892 USA;

    Natl Inst Dent &

    Craniofacial Res Oral Immunobiol Unit NIH 30 Convent Dr Bldg 30 Room 301 MSC;

    NCI Immune Deficiency Cellular Therapy Program Ctr Canc Res NIH 9000 Rockville Pike Bldg 10;

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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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