Addition of single dose gemtuzumab ozogamicin to intensive induction chemotherapy in core-binding factor acute myeloid leukemia

IF 2.1 4区 医学 Q3 HEMATOLOGY Leukemia research Pub Date : 2024-02-28 DOI:10.1016/j.leukres.2024.107467
Garrett Bourne , Kendall Diebold , Manuel Espinoza-Gutarra , Zaid Al-Kadhimi , Kimo Bachiashvili , Sravanti Rangaraju , Pankit Vachhani , Ravi Bhatia , Omer Jamy
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Abstract

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/m2, 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.

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在核心结合因子急性髓性白血病强化诱导化疗中加入单剂量吉妥珠单抗-奥佐加米星
一项对5项试验进行的荟萃分析显示,在强化诱导化疗的基础上加用吉妥珠单抗-奥佐米星(GO)可使核心结合因子(CBF)急性髓性白血病(AML)患者的生存获益。鉴于GO在临床试验中的应用不尽相同,理想的剂量和疗程仍不明确。我们进行了一项单中心回顾性分析,比较了仅在诱导期间接受强化诱导化疗的 CBF-AML 患者的疗效,以及是否单剂量使用 3mg/m GO。我们纳入了 87 例患者(GO=32 例,对照组=55 例)。对照组的综合完全缓解(cCR)率(93%)高于 GO 组(82%)(P<0.001)。通过流式细胞术检测,两组的可测量残留疾病(MRD)阴性 cCR 率相似。两组在毒性方面无明显差异。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%,而对照组为66%(P=0.9)。我们发现,在现实世界中,CBF-AML 患者的生存率较高。与不使用GO的强化化疗相比,在诱导期间加用单剂量GO并不能提高缓解率或生存率。需要进一步研究将 GO 纳入 CBF-AML 治疗方案的可能性。
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来源期刊
Leukemia research
Leukemia research 医学-血液学
CiteScore
4.00
自引率
3.70%
发文量
259
审稿时长
1 months
期刊介绍: Leukemia Research an international journal which brings comprehensive and current information to all health care professionals involved in basic and applied clinical research in hematological malignancies. The editors encourage the submission of articles relevant to hematological malignancies. The Journal scope includes reporting studies of cellular and molecular biology, genetics, immunology, epidemiology, clinical evaluation, and therapy of these diseases.
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