Divisions of Hematology, Mayo Clinic, Rochester, Minnesota.
Division of Hematology and Medical Oncology, Department of Medicine, Mayo Clinic, Phoenix, Arizona.
Am J Hematol. 2018 May;93(5):649-654. doi: 10.1002/ajh.25053. Epub 2018 Feb 24.
The prognostic importance of genetic information in primary myelofibrosis (PMF) was recently highlighted in a study of over 1000 cytogenetically-annotated patients; 5-year survival rates were 8% for very high risk (VHR), 27% "unfavorable" and 45% "favorable" karyotype. The current study addresses the practice-relevant question of whether or not allogeneic hematopoietic stem cell transplant (HCT) can overcome the detrimental survival effect of VHR or unfavorable karyotype. The study included 67 patients with PMF or secondary MF who received HCT at the Mayo Clinic and in whom pretransplant cytogenetic information was available. Dynamic international prognostic scoring system (DIPSS) risk distribution was 13% high, 66% intermediate-2 and 21% intermediate-1. Cytogenetic risk distribution was 11% VHR, 34% unfavorable and 55% favorable. At median post-HCT follow-up of 60 months for living patients (range 34-170), 28 (42%) deaths were recorded. Five-year survival was 62% and was not affected by VHR or unfavorable karyotype (P = .68). The salutary effect of HCT in patients with VHR or unfavorable karyotype was also apparent during analysis of a combined dataset that included a nontransplant cohort of 383 patients with PMF; multivariable analysis of the combined dataset (n = 450) resulted in HRs (95% CI) of 2.4 (1.6-3.6) for absence of transplant, 3.3 (2.2-4.8) for VHR karyotype, 1.6 (1.2-2.1) for unfavorable karyotype, 2.9 (2.0-4.2) for DIPSS high and 1.7 (1.4-2.2) for DIPSS intermediate-2. These observations were further confirmed by analysis of more stringently matched case-control subset cohorts and provide the evidence for the therapeutic preference of HCT in cytogenetically high risk patients with MF.
原发性骨髓纤维化(PMF)中遗传信息的预后重要性最近在一项超过 1000 例细胞遗传学注释患者的研究中得到了强调;5 年生存率分别为非常高风险(VHR)为 8%,“不利”为 27%,“有利”核型为 45%。本研究解决了一个实践相关的问题,即同种异体造血干细胞移植(HCT)是否可以克服 VHR 或不利核型的有害生存效应。该研究包括在梅奥诊所接受 HCT 治疗且移植前细胞遗传学信息可用的 67 例 PMF 或继发性 MF 患者。动态国际预后评分系统(DIPSS)风险分布为 13%高风险,66%中-2 风险,21%中-1 风险。细胞遗传学风险分布为 11%VHR,34%不利核型,55%有利核型。在有存活患者的中位移植后随访 60 个月(范围 34-170)时,记录了 28 例(42%)死亡。5 年生存率为 62%,不受 VHR 或不利核型的影响(P = .68)。在包括 383 例 PMF 非移植队列的联合数据集的分析中,HCT 在 VHR 或不利核型患者中的有益作用也很明显;联合数据集(n = 450)的多变量分析得出的风险比(95%CI)分别为无移植的 2.4(1.6-3.6)、VHR 核型的 3.3(2.2-4.8)、不利核型的 1.6(1.2-2.1)、DIPSS 高的 2.9(2.0-4.2)和 DIPSS 中-2 的 1.7(1.4-2.2)。这些观察结果通过更严格匹配病例对照亚组队列的分析得到了进一步证实,并为 HCT 在细胞遗传学高危 PMF 患者中的治疗偏好提供了证据。