Sylvie D. Freeman and Naeem Khan, University of Birmingham, Birmingham; Robert K. Hills, Amanda Gilkes, Laura Upton, Ian Thomas, and Alan K. Burnett, Cardiff University; Steve Couzens University Hospital of Wales, Cardiff; Paul Virgo, North Bristol NHS Trust, Bristol; Richard Dillon and David Grimwade, King's College London School of Medicine; James D. Cavenagh, Queen Mary University of London; Asim Khwaja, University College London, London; Gail Jones, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle; Paul Cahalin, Blackpool Teaching Hospital NHS Foundation Trust, Blackpool; Nigel H. Russell, Nottingham University Hospital, Nottingham, United Kingdom; Ove Juul Nielsen, Rigshospitalet, Copenhagen, Denmark.
J Clin Oncol. 2018 May 20;36(15):1486-1497. doi: 10.1200/JCO.2017.76.3425. Epub 2018 Mar 30.
Purpose We investigated the effect on outcome of measurable or minimal residual disease (MRD) status after each induction course to evaluate the extent of its predictive value for acute myeloid leukemia (AML) risk groups, including NPM1 wild-type (wt) standard risk, when incorporated with other induction response criteria. Methods As part of the NCRI AML17 trial, 2,450 younger adult patients with AML or high-risk myelodysplastic syndrome had prospective multiparameter flow cytometric MRD (MFC-MRD) assessment. After course 1 (C1), responses were categorized as resistant disease (RD), partial remission (PR), and complete remission (CR) or complete remission with absolute neutrophil count < 1,000/µL or thrombocytopenia < 100,000/μL (CRi) by clinicians, with CR/CRi subdivided by MFC-MRD assay into MRD+ and MRD-. Patients without high-risk factors, including Flt3 internal tandem duplication wt/- NPM1-wt subgroup, received a second daunorubicin/cytosine arabinoside induction; course 2 (C2) was intensified for patients with high-risk factors. Results Survival outcomes from PR and MRD+ responses after C1 were similar, particularly for good- to standard-risk subgroups (5-year overall survival [OS], 27% RD v 46% PR v 51% MRD+ v 70% MRD-; P < .001). Adjusted analyses confirmed significant OS differences between C1 RD versus PR/MRD+ but not PR versus MRD+. CRi after C1 reduced OS in MRD+ (19% CRi v 45% CR; P = .001) patients, with a smaller effect after C2. The prognostic effect of C2 MFC-MRD status (relapse: hazard ratio [HR], 1.88 [95% CI, 1.50 to 2.36], P < .001; survival: HR, 1.77 [95% CI, 1.41 to 2.22], P < .001) remained significant when adjusting for C1 response. MRD positivity appeared less discriminatory in poor-risk patients by stratified analyses. For the NPM1-wt standard-risk subgroup, C2 MRD+ was significantly associated with poorer outcomes (OS, 33% v 63% MRD-, P = .003; relapse incidence, 89% when MRD+ ≥ 0.1%); transplant benefit was more apparent in patients with MRD+ (HR, 0.72; 95% CI, 0.31 to 1.69) than those with MRD- (HR, 1.68 [95% CI, 0.75 to 3.85]; P = .16 for interaction). Conclusion MFC-MRD can improve outcome stratification by extending the definition of partial response after first induction and may help predict NPM1-wt standard-risk patients with poor outcome who benefit from transplant in the first CR.
我们研究了每个诱导疗程后可测量或最小残留疾病(MRD)状态对预后的影响,以评估其对急性髓系白血病(AML)风险组的预测价值的程度,包括 NPM1 野生型(wt)标准风险,当与其他诱导反应标准结合使用时。
作为 NCRI AML17 试验的一部分,2450 名年轻成年 AML 或高危骨髓增生异常综合征患者前瞻性进行多参数流式细胞术 MRD(MFC-MRD)评估。在第 1 个疗程(C1)后,根据临床医生的评估,反应分为耐药疾病(RD)、部分缓解(PR)和完全缓解(CR)或完全缓解伴绝对中性粒细胞计数<1000/µL 或血小板计数<100000/μL(CRi),CR/CRi 通过 MFC-MRD 检测进一步分为 MRD+和 MRD-。无 Flt3 内部串联重复 wt/-NPM1-wt 亚组等高危因素的患者接受第二个柔红霉素/阿糖胞苷诱导;高危患者的第 2 个疗程(C2)强化治疗。
C1 后 PR 和 MRD+反应的生存结果相似,尤其是在良好至标准风险亚组中(5 年总生存率[OS],RD 为 27%,PR 为 46%,MRD+为 51%,MRD-为 70%;P<0.001)。调整分析证实 C1 RD 与 PR/MRD+之间存在显著的 OS 差异,但 PR 与 MRD+之间无差异。C1 后 CRi 降低了 MRD+患者的 OS(CRi 为 19%,CR 为 45%;P=0.001),C2 后影响较小。C2 MFC-MRD 状态(复发:危险比[HR],1.88[95%CI,1.50 至 2.36],P<0.001;生存:HR,1.77[95%CI,1.41 至 2.22],P<0.001)的预后效应在调整 C1 反应后仍然显著。分层分析表明,MRD 阳性在预后不良的患者中缺乏区分力。对于 NPM1-wt 标准风险亚组,C2 MRD+与较差的预后显著相关(OS,MRD-为 63%,MRD+为 33%,P=0.003;复发发生率,MRD+≥0.1%时为 89%);移植获益在 MRD+患者中更为明显(HR,0.72;95%CI,0.31 至 1.69),而在 MRD-患者中则不明显(HR,1.68[95%CI,0.75 至 3.85];P=0.16 用于交互作用)。
MFC-MRD 可以通过扩展第一个诱导疗程后部分缓解的定义来改善预后分层,并可能有助于预测 NPM1-wt 标准风险患者的预后不良,这些患者在第一个 CR 中受益于移植。