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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Residual disease detected by multidimensional flow cytometry signifies high relapse risk in patients with de novo acute myeloid leukemia: A report from Children's Oncology Group
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Residual disease detected by multidimensional flow cytometry signifies high relapse risk in patients with de novo acute myeloid leukemia: A report from Children's Oncology Group

机译:多维流式细胞仪检测到的残留疾病预示着急性髓样白血病患者的高复发风险:儿童肿瘤学组的一份报告

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Early response to induction chemotherapy is a predictor of outcome in acute myeloid leukemia (AML). We determined the prevalence and significance of postinduction residual disease (RD) by multidimensional flow cytometry (MDF) in children treated on Children's Oncology Group AML protocol AAML03P1. Postinduction marrow specimens at the end of induction (EOI) 1 or 2 or at the end of therapy from 249 patients were prospectively evaluated by MDF for RD, and presence of RD was correlated with disease characteristics and clinical outcome. Of the 188 patients in morphologic complete remission at EOI1, 46 (24%) had MDFdetectable disease. Those with and without RD at the EOI1 had a 3-year relapse risk of 60% and 29%, respectively (P < .001); the corresponding relapsefree survival was 30% and 65% (P < .001). Presence of RD at the EOI2 and end of therapy was similarly predictive of poor outcome. RD was detected in 28% of standard-risk patients in complete remission and was highly associated with poor relapse-free survival (P = .008). In a multivariate analysis, including cytogenetic and molecular risk factors, RD was an independent predictor of relapse (P < .001). MDF identifies patients at risk of relapse and poor outcome and can be incorporated into clinical trials for riskbased therapy allocation. This study was registered at www.clinicaltrials.gov as NCT00070174.
机译:诱导化疗的早期反应是急性髓细胞性白血病(AML)的预后指标。我们通过多维流式细胞术(MDF)确定了在儿童肿瘤学组AML协议AAML03P1上治疗的儿童中诱导后残留疾病(RD)的患病率和意义。 MDF对249名患者的诱导结束(EOI)1或2或治疗结束时的诱导后骨髓标本进行RD前瞻性评估,RD的存在与疾病特征和临床结果相关。在EOI1形态完全缓解的188例患者中,有46例(24%)患有MDF可检测的疾病。在EOI1处有RD和无RD的患者3年复发风险分别为60%和29%(P <.001);相应的无复发生存率分别为30%和65%(P <.001)。 EOI2和治疗结束时RD的存在也预示了不良预后。在完全缓解的标准风险患者中,有28%检测到RD,并与不良的无复发生存高度相关(P = .008)。在包括细胞遗传和分子危险因素在内的多变量分析中,RD是复发的独立预测因子(P <.001)。 MDF可以识别有复发风险和不良预后的患者,可以纳入基于风险的治疗分配的临床试验中。该研究已在www.clinicaltrials.gov上注册为NCT00070174。

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