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Quantitative chimerism: an independent acute leukemia prognosis indicator following allogeneic hematopoietic SCT.

机译:定量嵌合:异基因造血SCT后独立的急性白血病预后指标。

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This study evaluates the prognostic significance of quantitative chimerism to monitor minimal residual disease and predict relapse in acute leukemia (AL) patients following allogeneic hematopoietic SCT (HSCT). The quantitative chimerism levels of 129 AL patients were measured using RQ-PCR based on 29 sequence polymorphisms. Receiver-operating characteristic curve indicated that the optimal cutoff point to predict an inevitable relapse was 1.0%, which results in 100.0% sensitivity and 79.6% specificity.The relapse rate of patients with chimerism >1.0% at 2 years was 55.0%, whereas that for patients with chimerism <1.0% was 0%(P=0.000). Quantitative chimerism >1.00% indicated a higher probability of relapse. Cox multivariate analysis indicated that quantitative chimerism >1.00% was associated with lower disease-free survival (hazard ratio (HR)=10.825; 95% confidence interval (CI) =4.704-24.912, P=0.000) and lower OS (HR=8.681; 95% CI=3.728-20.212, P=0.000). Patients (24/47 with quantitative chimerism >1.00%) who received preemptive modified DLI immunotherapy had significantly lower relapse rate (37.5%) than those (n=9) who did not (100%; P=0.001). Thus, quantitative chimerism is an independent prognostic factor that predicts clinical outcomes after HSCT and provides a guide for suitable interventions.
机译:这项研究评估了定量嵌合体在监测异基因造血SCT(HSCT)后急性白血病(AL)患者中的最小残留疾病并预测复发的预后意义。使用RQ-PCR基于29个序列多态性,测量了129名AL患者的定量嵌合水平。接受者操作特征曲线表明,预测不可避免的复发的最佳临界点为1.0%,这导致100.0%的敏感性和79.6%的特异性;嵌合度> 1.0%的患者2年的复发率为55.0%,而嵌合率<1.0%的患者为0%(P = 0.000)。定量嵌合率> 1.00%表示复发的可能性更高。 Cox多变量分析表明,定量嵌合率> 1.00%与较低的无病生存率(危险比(HR)= 10.825; 95%置信区间(CI)= 4.704-24.912,P = 0.000)和OS较低(HR = 8.681)相关; 95%CI = 3.728-20.212,P = 0.000)。预先接受改良DLI免疫疗法的患者(24/47的定量嵌合率> 1.00%)的复发率(37.5%)显着低于未接受DLI免疫治疗的患者(n = 9)(100%; P = 0.001)。因此,定量嵌合是一种独立的预后因素,可预测HSCT后的临床结果,并为适当的干预措施提供指导。

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