Hematologics, Inc, Seattle, WA.
Children's Oncology Group, Monrovia, CA.
Blood Adv. 2020 Oct 27;4(20):5050-5061. doi: 10.1182/bloodadvances.2020002070.
Risk stratification for acute myeloid leukemia (AML) uses molecular and cytogenetic abnormalities identified at diagnosis. Response to therapy informs risk, and morphology continues to be used more frequently than flow cytometry. Herein, the largest cohort of pediatric patients prospectively assessed for measurable residual disease (MRD) by flow cytometry (N = 784) is reported. The "difference from normal" (ΔN) technique was applied: 31% of all patients tested positive (AML range, 0.02% to 91%) after the first course of treatment on Children's Oncology Group study AAML0531. Detection of MRD following initial chemotherapy proved the strongest predicator of overall survival (OS) in univariable and multivariable analyses, and was predictive of relapse risk, disease-free survival, and treatment-related mortality. Clearance of MRD after a second round of chemotherapy did not improve survival. The morphologic definition of persistent disease (>15% AML) failed 27% of the time; those identified as MRD- had superior outcomes. Similarly, for patients not achieving morphologic remission (>5% blasts), 36% of patients were MRD- and had favorable outcomes compared with those who were MRD+ (P < .001); hence an increase in myeloid progenitor cells can be favorable when ΔN classifies them as phenotypically normal. Furthermore, ΔN reclassified 20% of patients in morphologic remission as having detectable MRD with comparable poor outcomes. Retrospective analysis using the relapse phenotype as a template demonstrated that 96% of MRD- patients had <0.02% of the relapse immunophenotype in their end of induction 1 marrow. Thus, the detection of abnormal myeloid progenitor cells by ΔN is both specific and sensitive, with a high predictive signal identifiable early in treatment. This trial was registered at www.clinicaltrials.gov as #NCT00372593.
急性髓系白血病(AML)的风险分层采用诊断时确定的分子和细胞遗传学异常。治疗反应可提示风险,形态学的使用频率继续高于流式细胞术。本文报告了迄今为止通过流式细胞术对最大儿科患者队列进行前瞻性评估的可测量残留疾病(MRD)(N=784)。应用了“与正常的差异”(ΔN)技术:在儿童肿瘤学组研究 AAML0531 的第一个疗程后,31%的所有患者检测结果为阳性(AML 范围为 0.02%至 91%)。初始化疗后检测到的 MRD 是单变量和多变量分析中总生存(OS)的最强预测因子,并且可预测复发风险、无病生存和治疗相关死亡率。第二轮化疗后 MRD 清除并未改善生存。形态学定义的持续性疾病(>15%AML)的失败率为 27%;被认为是 MRD-的患者具有更好的结局。同样,对于未达到形态学缓解(>5%blasts)的患者,36%的患者是 MRD-,与 MRD+的患者相比具有良好的结局(P<0.001);因此,当ΔN 将髓系祖细胞归类为表型正常时,其增加可能是有利的。此外,ΔN 将 20%的形态学缓解患者重新分类为可检测到的 MRD,其结果相似。使用复发表型进行回顾性分析表明,96%的 MRD-患者在诱导结束 1 期骨髓中复发免疫表型<0.02%。因此,通过 ΔN 检测异常髓系祖细胞既具有特异性又具有敏感性,在治疗早期即可识别出具有高预测信号的异常。该试验在 www.clinicaltrials.gov 上注册,编号为 #NCT00372593。