Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Center for Research and Application of Cellular Therapy, Kyoto University Hospital, Kyoto, Japan.
Br J Haematol. 2023 Jul;202(2):356-368. doi: 10.1111/bjh.18855. Epub 2023 May 21.
To evaluate the prognostic impact of complex karyotype (CK) and/or monosomal karyotype (MK) in combination with various clinical factors on allogeneic stem cell transplantation (HSCT) outcomes of patients with acute myeloid leukaemia (AML), we analysed the registry database of adult AML patients who underwent allogeneic HSCT between 2000 and 2019 in Japan. Among 16 094 patients, those with poor cytogenetic risk (N = 3345) showed poor overall survival (OS) after HSCT (25.3% at 5 years). Multivariate analyses revealed that CK and/or MK (hazard ratio [HR], 1.31 for CK without MK; 1.27 for MK without CK; and 1.73 for both), age at HSCT ≥50 years (HR, 1.58), male sex (HR, 1.40), performance status ≥2 (HR, 1.89), HCT-CI score ≥3 (HR, 1.23), non-remission status at HSCT (HR, 2.49), and time from diagnosis to HSCT ≥3 months (HR, 1.24) independently reduced post-HSCT OS among patients with poor cytogenetic risk AML. A risk scoring system based on the multivariate analysis successfully stratified patients into five distinct groups for OS. This study confirms the negative effects of CK and MK on post-HSCT outcomes, and offers a powerful risk scoring system for predicting prognoses after HSCT among AML patients with unfavourable cytogenetics.
为了评估复杂核型(CK)和/或单体核型(MK)与各种临床因素相结合对接受异基因造血干细胞移植(HSCT)的急性髓系白血病(AML)患者预后的影响,我们分析了 2000 年至 2019 年间在日本接受异基因 HSCT 的成人 AML 患者的注册数据库。在 16094 例患者中,不良细胞遗传学风险患者(N=3345)在 HSCT 后总体生存(OS)较差(5 年时为 25.3%)。多变量分析显示 CK 和/或 MK(危险比[HR],无 MK 的 CK 为 1.31;无 CK 的 MK 为 1.27;两者均为 1.73)、HSCT 时年龄≥50 岁(HR,1.58)、男性(HR,1.40)、体能状态≥2(HR,1.89)、HCT-CI 评分≥3(HR,1.23)、HSCT 时未缓解(HR,2.49)和从诊断到 HSCT 的时间≥3 个月(HR,1.24)独立降低了不良细胞遗传学 AML 患者 HSCT 后的 OS。基于多变量分析的风险评分系统成功地将患者分为五个不同的 OS 组。这项研究证实了 CK 和 MK 对 HSCT 后结局的负面影响,并为预测不良细胞遗传学 AML 患者 HSCT 后预后提供了一种强大的风险评分系统。