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高剂量阿糖胞苷联合吉妥珠单抗奥唑米星作为中低危急性髓系白血病患者的巩固治疗。

High-dose cytarabine plus gemtuzumab ozogamicin as consolidation therapy in patients with favorable- or intermediate-risk acute myeloid leukemia.

机构信息

Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine, 67 Asahi-Machi, Kurume, 830-0011, Japan.

Department of Medicine, Inuzuka Hospital, Kashima, Saga, Japan.

出版信息

Int J Hematol. 2024 Sep;120(3):297-304. doi: 10.1007/s12185-024-03814-z. Epub 2024 Jul 4.

Abstract

Previous prospective randomized trials have investigated the efficacy of gemtuzumab ozogamicin in the frontline treatment of acute myeloid leukemia (AML). We evaluated the efficacy of high-dose cytarabine with GO as consolidation therapy in 20 patients with favorable- or intermediate-risk AML in first complete remission. They included six patients with wild-type nucleophosmin (NPM1) core binding factor (CBF), ten with NPM1-mutated non-CBF, and four with wild-type NPM1 non-CBF. The median follow-up for the entire cohort was 62.0 months. The three-year overall survival (OS) and relapse-free survival (RFS) rates were 72.2% and 77.8%, respectively. OS and RFS were significantly higher for NPM1-mutated non-CBF AML than for wild-type NPM1 non-CBF AML (p = 0.001). We also examined the CD33 single-nucleotide polymorphism (SNP) rs12459419, which has been reported to influence the therapeutic efficacy of GO and CD33 expression. The CD33 expression ratio was higher in CD33 SNP C/C than in C/T (83.1% vs. 49.8%, p = 0.035), but 3-year OS and RFS did not differ significantly. These results suggest that consolidation therapy with high-dose cytarabine plus GO is highly effective in transplant-ineligible elderly patients and may be a reasonable treatment, especially for NPM1-mutated AML.

摘要

先前的前瞻性随机试验已经研究了吉妥珠单抗奥佐米星在急性髓系白血病(AML)一线治疗中的疗效。我们评估了高剂量阿糖胞苷联合 GO 作为 20 例处于完全缓解期的初治伴有利或中等风险 AML 患者巩固治疗的疗效。这些患者包括 6 例野生型核磷蛋白(NPM1)核心结合因子(CBF)AML、10 例 NPM1 突变非 CBF AML 和 4 例野生型 NPM1 非 CBF AML。整个队列的中位随访时间为 62.0 个月。总生存率(OS)和无复发生存率(RFS)分别为 72.2%和 77.8%。NPM1 突变非 CBF AML 的 OS 和 RFS 显著高于野生型 NPM1 非 CBF AML(p=0.001)。我们还检查了 CD33 单核苷酸多态性(SNP)rs12459419,该 SNP 已被报道影响 GO 和 CD33 表达的治疗效果。CD33 SNP C/C 的 CD33 表达比值高于 C/T(83.1%比 49.8%,p=0.035),但 3 年 OS 和 RFS 无显著差异。这些结果表明,高剂量阿糖胞苷联合 GO 巩固治疗对不适合移植的老年患者非常有效,可能是一种合理的治疗方法,尤其是对 NPM1 突变 AML。

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