Department of Internal Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Division of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Leuk Res. 2024 Apr;139:107467. doi: 10.1016/j.leukres.2024.107467. Epub 2024 Feb 28.
In a meta-analysis of 5 trials, the addition of gemtuzumab ozogamicin (GO) to intensive induction chemotherapy led to a survival benefit in patients with core-binding factor (CBF) acute myeloid leukemia (AML). Given the heterogeneous incorporation of GO in clinical trials, the ideal dose and schedule remains unclear. We conducted a single-center retrospective analysis to compare outcomes of patients with CBF-AML treated with intensive induction chemotherapy, with or without a single dose of GO 3 mg/m, during induction only. We included 87 patients (GO=32, control=55). The composite complete remission (cCR) rate was higher in the control group (93%) compared to the GO group (82%) (p<0.001). The rate of measurable residual disease (MRD) negative cCR, by flow cytometry, was similar between both groups. There were no significant differences between the two groups in terms of toxicity. The 3-year relapse-free survival (RFS) for both groups was similar (71% vs 68%, p=0.5). The 3-year overall survival (OS) for the GO group was 68%, compared to 66% for the control group (p=0.9).In multivariable analysis, age and MRD positive status were risk factors for inferior outcomes. We find that survival of patients with CBF-AML is favorable in the real-world setting. The addition of single-dose GO, during induction, did not lead to a higher remission rate or survival benefit, when compared to intensive chemotherapy without GO. Further investigation into the incorporation of GO in the treatment algorithm for CBF-AML is needed.
在五项试验的荟萃分析中,添加吉妥珠单抗奥佐米星(GO)到强化诱导化疗可使核心结合因子(CBF)急性髓细胞白血病(AML)患者获益。鉴于 GO 在临床试验中的异质性纳入,理想的剂量和方案仍不清楚。我们进行了一项单中心回顾性分析,比较了接受强化诱导化疗的 CBF-AML 患者的结局,这些患者在诱导期仅接受了单次 3mg/m 的 GO 或不接受 GO。我们纳入了 87 例患者(GO=32,对照组=55)。对照组的完全缓解率(cCR)高于 GO 组(93% vs 82%)(p<0.001)。流式细胞术检测到两组的微小残留病(MRD)阴性 cCR 率相似。两组在毒性方面无显著差异。两组的 3 年无复发生存率(RFS)相似(71% vs 68%,p=0.5)。GO 组的 3 年总生存率(OS)为 68%,对照组为 66%(p=0.9)。多变量分析显示,年龄和 MRD 阳性状态是预后不良的危险因素。我们发现 CBF-AML 患者的生存状况在真实环境中良好。与未接受 GO 的强化化疗相比,在诱导期添加单次剂量的 GO 并未导致更高的缓解率或生存获益。需要进一步研究将 GO 纳入 CBF-AML 的治疗方案。