Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Am J Hematol. 2018 Aug;93(4):546-552. doi: 10.1002/ajh.25030. Epub 2018 Jan 27.
HyperCVAD is a commonly-used regimen for adults with newly-diagnosed acute lymphoblastic leukemia (ALL). However, relatively little is known about the application of minimal residual disease (MRD) detection with this treatment. To address this, we studied 142 adults with ALL treated with hyperCVAD over a 10-year period who had MRD assessed by either multi-parameter flow cytometry or (for patients with Philadelphia chromosome positive ALL) reverse transcriptase polymerase chain reaction for the BCR-ABL1 translocation. In a multivariate analysis, patients who achieved MRD negativity (MRD ) at any point had significantly better overall survival (OS; hazard ratio [HR] 0.43; P = .01) and event-free survival (EFS; HR 0.27; P < .01). Of 121 patients with MRD assessed at various points within 90 days of starting hyperCVAD, 50% (n = 61) had achieved MRD . Among those that became MRD , the median time to MRD was 68 days. Time to MRD was significantly associated with EFS (P = .009), but not OS (P = .19), implying increasingly better EFS the earlier MRD is achieved. These data add to our understanding of MRD assessment during treatment with hyperCVAD, aide clinicians with predicting relapse risk, and provide additional historical data on which future clinical trials can be designed.
HyperCVAD 是一种常用于治疗成人新发急性淋巴细胞白血病(ALL)的方案。然而,对于这种治疗方法中微小残留病(MRD)检测的应用,人们了解甚少。为了解决这个问题,我们研究了 142 名在过去 10 年中接受 HyperCVAD 治疗的 ALL 成年患者,这些患者通过多参数流式细胞术或(对于费城染色体阳性 ALL 患者)逆转录酶聚合酶链反应评估 MRD,检测 BCR-ABL1 易位。在多变量分析中,任何时间点达到 MRD 阴性(MRD )的患者总体生存率(OS;风险比 [HR] 0.43;P = .01)和无事件生存率(EFS;HR 0.27;P < .01)均显著提高。在开始接受 HyperCVAD 治疗的 90 天内,对 121 名患者的 MRD 进行了评估,其中 50%(n = 61)达到了 MRD 阴性。在达到 MRD 阴性的患者中,MRD 的中位时间为 68 天。MRD 的时间与 EFS 显著相关(P = .009),但与 OS 无关(P = .19),这表明 MRD 越早达到,EFS 越好。这些数据增加了我们对 HyperCVAD 治疗期间 MRD 评估的理解,有助于临床医生预测复发风险,并为未来的临床试验提供了额外的历史数据。