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首页> 外文期刊>Journal of Clinical Oncology >Analysis of risk factors for outcomes after unrelated cord blood transplantation in adults with lymphoid malignancies: a study by the Eurocord-Netcord and lymphoma working party of the European group for blood and marrow transplantation.
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Analysis of risk factors for outcomes after unrelated cord blood transplantation in adults with lymphoid malignancies: a study by the Eurocord-Netcord and lymphoma working party of the European group for blood and marrow transplantation.

机译:成人淋巴恶性肿瘤无关脐带血移植后结局的危险因素分析:欧洲小组血液和骨髓移植的Eurocord-Netcord和淋巴瘤工作组进行的一项研究。

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PURPOSE: To determine risk factors of umbilical cord blood transplantation (UCBT) for patients with lymphoid malignancies. PATIENTS AND METHODS: We evaluated 104 adult patients (median age, 41 years) who underwent unrelated donor UCBT for lymphoid malignancies. UCB grafts were two-antigen human leukocyte antigen-mismatched in 68%, and were composed of one (n = 78) or two (n = 26) units. Diagnoses were non-Hodgkin's lymphoma (NHL, n = 61), Hodgkin's lymphoma (HL, n = 29), and chronic lymphocytic leukemia (CLL, n = 14), with 87% having advanced disease and 60% having experienced failure with a prior autologous transplant. Sixty-four percent of patients received a reduced-intensity conditioning regimen and 46% low-dose total-body irradiation (TBI). Median follow-up was 18 months. RESULTS: Cumulative incidence of neutrophil engraftment was 84% by day 60, with greater engraftment in recipients of higher CD34(+) kg/cell dose (P = .0004). CI of non-relapse-related mortality (NRM) was 28% at 1 year, with a lower risk in patients treated with low-dose total-body irradiation (TBI; P = .03). Cumulative incidence of relapse or progression was 31% at 1 year, with a lower risk in recipients of double-unit UCBT (P = .03). The probability of progression-free survival (PFS) was 40% at 1 year, with improved survival in those with chemosensitive disease (49% v 34%; P = .03), who received conditioning regimens containing low-dose TBI (60% v 23%; P = .001), and higher nucleated cell dose (49% v 21%; P = .009). CONCLUSION: UCBT is a viable treatment for adults with advanced lymphoid malignancies. Chemosensitive disease, use of low-dose TBI, and higher cell dose were factors associated with significantly better outcome.
机译:目的:确定淋巴恶性肿瘤患者脐带血移植(UCBT)的危险因素。患者与方法:我们评估了104例接受无关供体UCBT的成人患者(中位年龄41岁)的淋巴恶性肿瘤。 UCB移植物是两种抗原的人类白细胞抗原不匹配,占68%,由一个(n = 78)或两个(n = 26)单位组成。诊断为非霍奇金淋巴瘤(NHL,n = 61),霍奇金淋巴瘤(HL,n = 29)和慢性淋巴细胞性白血病(CLL,n = 14),其中87%患有晚期疾病,60%经历失败并伴有事先进行自体移植。 64%的患者接受了降低强度的调理方案和46%的低剂量全身照射(TBI)。中位随访时间为18个月。结果:到第60天,中性粒细胞植入的累积发生率为84%,较高的CD34(+)kg /细胞剂量的接受者的植入发生率更高(P = .0004)。 1年非复发相关死亡率(NRM)的CI为28%,接受低剂量全身照射治疗的患者的风险较低(TBI; P = .03)。一年内复发或进展的累积发生率为31%,双单位UCBT的接受者风险较低(P = .03)。接受低剂量TBI调理方案(60%)的化学敏感性疾病患者(1%)的无进展生存(PFS)概率为40%(49%vs 34%; P = .03)。 v 23%; P = .001)和更高的有核细胞剂量(49%v 21%; P = .009)。结论:UCBT对于成人晚期淋巴恶性肿瘤是一种可行的治疗方法。化学敏感性疾病,使用低剂量TBI和较高细胞剂量是与明显改善预后相关的因素。

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