This multicenter retrospective study by GETH-TC validates the prognostic value of the Allo-HCT Refined ELN 2022 risk classification in allografted AML patients. The new classification refines the ELN 2022 risk classification, dividing adverse-risk patients into two subgroups: Adv-Plus (AdvP), including those with complex karyotype, MECOM (EVI1) rearrangement, or TP53 mutations/del(17p), and an additional adverse group (Adv*). The study included 651 AML patients treated with at least one line of anthracycline-based induction therapy and in complete remission. According to the Allo-HCT Refined ELN 2022 risk classification, 19.4% (n = 126) patients were classified into the Favorable (Fav) risk, 38.1% (n = 248) into the Intermediate (Int) risk, 27.2% (n = 177) in the Adv* and 15.4% (n = 100) in the AdvP. Outcomes were significantly poorer for patients allocated in the AdvP risk group (5-year OS rate: 32.3%, 5-year LFS rate: 24.3%, both p < 0.001 with the rest of subgroups) and a higher CIR (5-year CIR: 64.3%, p < 0.001). Patients in the Adv* risk group had similar outcomes than patients in the Int risk group (5-year OS rate: 70.2% vs. 66.7%, p = 0.69, 5-year LFS rate: 63.8% vs. 55.9%, p = 0.33). Multivariate analysis confirmed the dismal outcomes for AdvP patients for OS: Hazard Ratio (HR) = 3.05, and LFS: HR = 2.66, both p < 0.001. Our findings validate the Allo-HCT Refined ELN 2022 classification as a robust prognostic tool, particularly highlighting the poor outcomes for the AdvP subgroup.
这项由GETH-TC开展的多中心回顾性研究验证了Allo-HCT改良版ELN 2022风险分层在接受异基因造血干细胞移植的AML患者中的预后价值。新分层方案在ELN 2022风险分类基础上进行改良,将高危患者分为两个亚组:极高危组(AdvP,包括复杂核型、MECOM(EVI1)重排或TP53突变/del(17p)患者)和其他高危组(Adv*)。该研究纳入651例接受至少一线蒽环类药物诱导治疗并获得完全缓解的AML患者。根据Allo-HCT改良版ELN 2022风险分层,19.4%(126例)患者属于低危组,38.1%(248例)为中危组,27.2%(177例)为Adv*组,15.4%(100例)为AdvP组。AdvP组患者预后显著更差(5年总生存率32.3%,5年无白血病生存率24.3%,均较其他亚组p<0.001),且累积复发率更高(5年CIR 64.3%,p<0.001)。Adv*组患者与中危组患者预后相似(5年总生存率70.2% vs. 66.7%,p=0.69;5年无白血病生存率63.8% vs. 55.9%,p=0.33)。多变量分析证实AdvP患者的总生存(风险比3.05)和无白血病生存(风险比2.66)均显著恶化(均p<0.001)。本研究验证了Allo-HCT改良版ELN 2022分层作为可靠预后工具的临床价值,尤其明确了AdvP亚组的不良预后特征。