Petermichl Verena, Fuchs Stefan, Weber Matthias, Gobat Katrin, Micheloud Charlotte, Graf Lukas, Gerth Yannick, Goede Jeroen S, Lehmann Thomas, Driessen Christoph, Mey Ulrich J M, Cathomas Richard, Cogliatti Sergio, Silzle Tobias
Clinic for Medical Oncology and Hematology, Cantonal Hospital St. Gallen, 9007 St. Gallen, Switzerland.
Department of Internal Medicine, Cantonal Hospital Graubünden, 7000 Chur, Switzerland.
Cancers (Basel). 2025 Aug 14;17(16):2658. doi: 10.3390/cancers17162658.
The AML60+ score has been proposed for risk stratification in intensively treated elderly patients with acute myeloid leukemia (AML) or high-risk myelodysplastic neoplasms (MDS). Its prognostic impact in patients treated with hypomethylating agents (HMA) is unknown. Patients ≥ 60 years of age diagnosed with AML or MDS/AML according to ICC2022 were eligible for this retrospective and multicenter chart review if they had received at least one cycle of HMA-based treatment. A cohort of 142 patients was analyzed. During follow-up (median 8 months), 114 patients died. The molecular Prognostic Score (mPRS) was available for 121 patients, the European Leukemia Net (ELN) 2022 classification for 117 patients, and the AML60+ for 105 patients. According to AML60+, 33 patients (31.4%) were classified as very poor risk, 36 (34.3%) as poor risk, and 34 (32.4%) as intermediate risk. Two patients (1.9%) were classified as favorable. Median overall survival (OS) was 21.7 months (mo) for the combined intermediate/favorable group, 7 mo for the poor risk group and 3 mo for the very poor risk group ( < 0.0001). Cox regression analysis (reference category: very poor) showed a significantly lower risk of death for both intermediate/favorable risk patients (HR 0.17, 95% CI 0.10-0.31, < 0.001) and poor risk patients (HR 0.47, 95% CI 0.28-0.78, = 0.004). The concordance score was 0.67 for AML60+, 0.60 for mPRS, and 0.58 for ELN2022. The AML60+ may represent a useful prognostic tool for elderly AML patients treated with HMA-based therapies. In particular, it could help to identify a group with a relatively favorable prognosis that is not clearly identified by the ELN2022 or the mPRS risk classification. However, analyses of larger cohorts are necessary to confirm our findings.
AML60+评分已被提出用于接受强化治疗的老年急性髓系白血病(AML)或高危骨髓增生异常综合征(MDS)患者的风险分层。其在接受去甲基化药物(HMA)治疗的患者中的预后影响尚不清楚。根据ICC2022诊断为AML或MDS/AML的≥60岁患者,如果他们接受了至少一个周期的基于HMA的治疗,则有资格纳入这项回顾性多中心病历审查。分析了142例患者队列。在随访期间(中位时间8个月),114例患者死亡。121例患者可获得分子预后评分(mPRS),117例患者可获得欧洲白血病网络(ELN)2022分类,105例患者可获得AML60+评分。根据AML60+评分,33例患者(31.4%)被分类为极低危,36例(34.3%)为低危,34例(32.4%)为中危。2例患者(1.9%)被分类为高危。中危/高危合并组的中位总生存期(OS)为21.7个月(mo),低危组为7个月,极低危组为3个月(<0.0001)。Cox回归分析(参考类别:极低危)显示,中危/高危患者(HR 0.17,95%CI 0.10 - 0.31,<0.001)和低危患者(HR 0.47,95%CI 0.28 - 0.78,=0.004)的死亡风险均显著降低。AML60+的一致性评分为0.67,mPRS为0.60,ELN2022为0.58。AML60+可能是接受基于HMA疗法的老年AML患者的一种有用的预后工具。特别是,它有助于识别出一组预后相对较好的患者,而这组患者在ELN2022或mPRS风险分类中并未被明确识别。然而,需要对更大的队列进行分析以证实我们的发现。