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急性髓系白血病患者口服阿扎胞苷维持治疗的真实世界治疗模式及疗效

Real-world treatment patterns and outcomes with oral azacitidine maintenance therapy in patients with acute myeloid leukemia.

作者信息

Leber Brian, Ruiz Marcia T, Elgendy Hany, Pettersson Filippa, Prebet Thomas, Vigil Carlos E, Parikh Rohan C, Korgaonkar Siddhi, Bello Fareedat, Davis Keith L, Gaugler Lona, Strocchia Maria, Sieluk Jan, Li Yeran, Schuh Andre C

机构信息

McMaster University, Hamilton, Ontario, Canada.

Bristol Myers Squibb, Princeton, New Jersey, USA.

出版信息

Cancer. 2025 Apr 15;131(8):e35845. doi: 10.1002/cncr.35845.

Abstract

INTRODUCTION

This study describes baseline and clinical characteristics, treatment patterns, survival, and safety outcomes of patients with acute myeloid leukemia (AML) who received oral azacitidine (oral-AZA) maintenance therapy in Canada following its approval in 2021.

METHODS

A retrospective, observational medical record review was conducted of patients with AML in remission after induction therapy and who initiated treatment with oral-AZA between March 2021 and July 2023 in Canada. Real-world relapse-free survival and overall survival outcomes were estimated using Kaplan-Meier methodology.

RESULTS

Data from 119 patients were analyzed. The median age at oral-AZA initiation was 62.5 years. Most patients had favorable (39.5%) or intermediate (39.5%) genetic risk per the 2017/2022 European LeukemiaNet classification. Nearly all patients (99.2%) received cytarabine-based induction regimens. A total of 55.5% of patients received consolidation therapy, with a median of two cycles. After a median follow-up of 9.4 months, 68.1% of all patients were still receiving oral-AZA at last follow-up. After oral-AZA treatment, 21.0% of patients relapsed. Rates of real-world relapse-free survival and overall survival at 12 months from oral-AZA initiation were 66.9% and 74.5%, respectively. During oral-AZA treatment, 67.2% of patients experienced ≥1 adverse event. Concomitant antiemetic treatment was received by 78.2% of patients.

CONCLUSION

These findings provide real-world evidence further supporting the use of oral-AZA as a standard-of-care maintenance therapy in current routine clinical practice for patients with AML in remission who do not receive hematopoietic stem cell transplantation. These results may inform a broader clinical audience because of the inclusion of patients with diverse demographic and clinical characteristics.

摘要

引言

本研究描述了2021年在加拿大获批后接受口服阿扎胞苷(oral-AZA)维持治疗的急性髓系白血病(AML)患者的基线和临床特征、治疗模式、生存率及安全性结果。

方法

对2021年3月至2023年7月在加拿大接受诱导治疗后缓解且开始口服阿扎胞苷治疗的AML患者进行回顾性观察病历审查。使用Kaplan-Meier方法估计实际无复发生存率和总生存率。

结果

分析了119例患者的数据。开始口服阿扎胞苷时的中位年龄为62.5岁。根据2017/2022年欧洲白血病网络分类,大多数患者具有良好(39.5%)或中等(39.5%)遗传风险。几乎所有患者(99.2%)接受了基于阿糖胞苷的诱导方案。共有55.5%的患者接受巩固治疗,中位疗程为两个周期。中位随访9.4个月后,在最后一次随访时,68.1%的患者仍在接受口服阿扎胞苷治疗。口服阿扎胞苷治疗后,21.0%的患者复发。从开始口服阿扎胞苷起12个月时的实际无复发生存率和总生存率分别为66.9%和74.5%。在口服阿扎胞苷治疗期间,67.2%的患者发生≥1次不良事件。78.2%的患者接受了联合止吐治疗。

结论

这些发现提供了实际证据,进一步支持在当前常规临床实践中,将口服阿扎胞苷用作未接受造血干细胞移植的缓解期AML患者的标准维持治疗。由于纳入了具有不同人口统计学和临床特征的患者,这些结果可能会为更广泛的临床受众提供参考。

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