Rojek Alexandra E, McCormick Benjamin J, Cwykiel Joanna, Odetola Oluwatobi, Abaza Yasmin, Nai Nhi, Foucar Charles E, Achar Rohan K, Shallis Rory M, Bradshaw Danielle, Standridge Meaghan, Kota Vamsi, Murthy Guru Subramanian Guru, Badar Talha, Patel Anand A
Department of Medicine Section of Hematology/Oncology University of Chicago Chicago Illinois USA.
Division of Hematology-Oncology Blood and Marrow Transplantation Program Mayo Clinic Jacksonville Florida USA.
EJHaem. 2024 Jul 24;5(4):728-737. doi: 10.1002/jha2.981. eCollection 2024 Aug.
Core-binding factor acute myeloid leukemia (CBF-AML) is characterized by the presence of inv(16)/t(16;16) or t(8;21) and is classified as a favorable risk by the 2022 European LeukemiaNet (ELN) guidelines. The CD33-targeting antibody-drug conjugate, gemtuzumab ozogamicin (GO), is commonly added to intensive chemotherapy (IC) in CBF-AML. We sought to compare outcomes in patients treated with IC with or without GO in CBF-AML. We included 200 patients with CBF-AML treated with IC across seven academic centers. Induction treatment regimens were categorized as IC alone, IC with GO, or IC with KIT inhibitor (dasatinib or midostaurin). Median follow-up for the whole cohort was 2.5 years. Three-year overall survival (OS) was 70% and 3-year event-free survival (EFS) was 51%. Patients treated with IC with GO experienced a 3-year EFS of 50% compared to those treated with IC alone who experienced a 3-year EFS of 47%, with no statistically significant difference ( = 0.62). Similarly, those treated with IC with GO did not experience an improved OS compared to those treated with IC alone ( = 0.67). Patients treated with IC with KIT inhibitor experienced a significantly improved 3-year EFS of 85% compared to those with IC with or without GO ( = 0.04). We find in our study that there is no survival benefit in patients treated with IC with the addition of GO; improved EFS was seen in patients with CBF-AML treated with IC plus KIT inhibitors, consistent with outcomes noted in prospective studies utilizing this approach.
核心结合因子急性髓系白血病(CBF-AML)的特征是存在inv(16)/t(16;16)或t(8;21),根据2022年欧洲白血病网(ELN)指南被归类为低危。靶向CD33的抗体药物偶联物吉妥珠单抗奥唑米星(GO)通常会被添加到CBF-AML的强化化疗(IC)中。我们试图比较在CBF-AML中接受IC联合或不联合GO治疗的患者的结局。我们纳入了在七个学术中心接受IC治疗的200例CBF-AML患者。诱导治疗方案分为单纯IC、IC联合GO或IC联合KIT抑制剂(达沙替尼或米哚妥林)。整个队列的中位随访时间为2.5年。三年总生存率(OS)为70%,三年无事件生存率(EFS)为51%。接受IC联合GO治疗的患者三年EFS为50%,而接受单纯IC治疗的患者三年EFS为47%,差异无统计学意义(P = 0.62)。同样,与单纯接受IC治疗的患者相比,接受IC联合GO治疗的患者OS并未改善(P = 0.67)。与接受IC联合或不联合GO治疗的患者相比,接受IC联合KIT抑制剂治疗的患者三年EFS显著提高,为85%(P = 0.04)。我们在研究中发现,在IC治疗中添加GO对患者没有生存益处;在接受IC加KIT抑制剂治疗的CBF-AML患者中观察到EFS有所改善,这与采用这种方法的前瞻性研究中所指出的结局一致。