Bataller Alex, Goulart Hannah E, Issa Ghayas C, DiNardo Courtney D, Daver Naval, Kadia Tapan, Bazinet Alexandre, Bouligny Ian M, Senapati Jayastu, Haddad Fadi G, Borthakur Gautam, Sasaki Koji, Short Nicholas J, Yilmaz Musa, Montalban-Bravo Guillermo, Tang Guiling, Loghavi Sanam, Garcia-Manero Guillermo, Ravandi Farhad, Kantarjian Hagop, Jabbour Elias
Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Hematopathology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Leukemia. 2025 May 9. doi: 10.1038/s41375-025-02634-2.
Acute myeloid leukemia (AML) with KMT2A rearrangement (KMT2Ar) has poor outcomes. We analyzed 1,611 patients with AML and 4.3% demonstrated rearrangements in KMT2A. Signaling-related genes (NRAS 30%, KRAS 23% and FLT3-TKD 16%) were the most frequently mutated in patients with KMT2Ar AML. Patients treated with intensive chemotherapy (IT) achieved a complete remission (CR)/CR with incomplete blood count recovery (CRi) rate of 81%, and when combined with venetoclax, the CR/CRi rate increased to 100%. Patients treated with low intensity treatment (LIT) achieved an CR/CRi rate of 33%, and when combined with venetoclax, the CR/CRi rate was 61%. For patients treated with IT, the 5-year overall survival (OS) and event-free survival (EFS) rates were 66% and 64%, respectively, compared with 7% in those treated with LIT. Thirty-nine patients (57%) underwent allogeneic stem cell transplantation after achieving CR/CRi. For patients treated with LIT, multivariate analysis demonstrated that N/KRAS mutations were predictive for OS (HR 2.93, 95% CI 1.18-7.29, P = 0.021) and EFS (HR 3.51, 95% CI 1.35-9.24, P = 0.01). In summary, outcomes in KMT2Ar AML have improved over years in patients treated with IT, whereas those treated with LIT continue to show poor survival, highlighting the need for novel combinations.
伴有KMT2A重排(KMT2Ar)的急性髓系白血病(AML)预后较差。我们分析了1611例AML患者,其中4.3%表现出KMT2A重排。信号相关基因(NRAS 30%、KRAS 23%和FLT3-TKD 16%)在伴有KMT2Ar的AML患者中突变最为频繁。接受强化化疗(IT)的患者完全缓解(CR)/血细胞计数未完全恢复的CR(CRi)率为81%,联合维奈克拉治疗时,CR/CRi率增至100%。接受低强度治疗(LIT)的患者CR/CRi率为33%,联合维奈克拉治疗时,CR/CRi率为61%。接受IT治疗的患者,5年总生存率(OS)和无事件生存率(EFS)分别为66%和64%,而接受LIT治疗的患者分别为7%。39例患者(57%)在达到CR/CRi后接受了异基因干细胞移植。对于接受LIT治疗的患者,多变量分析表明N/KRAS突变可预测OS(HR 2.93,95%CI 1.18-7.29,P = 0.021)和EFS(HR 3.51,95%CI 1.35-9.24,P = 0.01)。总之,多年来接受IT治疗的伴有KMT2Ar的AML患者的预后有所改善,而接受LIT治疗的患者生存率仍然较低,这突出了对新型联合治疗方案的需求。