Oral Versus Intravenous Hypomethylating Agents in Myelodysplastic Syndromes and Acute Myeloid Leukemia: A Multicenter Real-World Toxicity Comparison.

IF 2.8 4区 医学 Q3 HEMATOLOGY
Reed Alexander Firestone, Julia Palecki, Maya Rosenberg, Jason Chen, Xiaoying Zheng, Eesha Balar, Niti Patel, Lindsay Wilde, Gina Keiffer, Jun Choi, Catherine Lai, Margaret T Kasner, Chetan Jeurkar
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引用次数: 0

Abstract

Background: Hypomethylating agents (HMAs) are a cornerstone of therapy for myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML). Oral formulations offer an alternative to intravenous (IV) administration, but comparative real-world toxicity data remain limited. We evaluated hematologic toxicity and adverse events associated with oral versus IV HMAs.

Methods: We conducted a multicenter retrospective cohort study of 33 patients with MDS or AML treated with oral decitabine/cedazuridine or oral azacitidine between January 1, 2016 and June 1, 2023 across three academic cancer centers. Twenty patients who also received IV HMAs were included in an intrapatient paired analysis. Cytopenias were assessed by absolute values and percent change from baseline to nadir. Wilcoxon signed-rank tests were used for intrapatient comparisons, and clinically significant adverse events were recorded descriptively.

Results: Among the 20 patients included in the intrapatient analysis, median decreases in hemoglobin were 20.8% during oral HMA therapy and 20.5% during IV HMA therapy. Median decreases in absolute neutrophil count were 95.9% and 97.3%, respectively, while median decreases in platelet count were 81.9% and 88.6%, respectively. No statistically significant differences were observed between oral and IV HMA therapy for hemoglobin (p = 0.60), absolute neutrophil count (p = 0.63), or platelet count (p = 0.06). Hospitalization occurred in 60.6% of patients during oral HMA therapy and 70.0% during IV HMA therapy, while neutropenic fever occurred in 51.5% and 60.0%, respectively.

Conclusions: Oral HMAs demonstrated cytopenia severity and adverse event rates comparable to IV HMAs, supporting oral formulations as a practical alternative in patients with MDS and AML. Although encouraging, these findings should be interpreted in the context of the retrospective design and modest sample size.

口服与静脉注射低甲基化药物治疗骨髓增生异常综合征和急性髓系白血病:多中心真实世界毒性比较
背景:低甲基化药物(HMAs)是骨髓增生异常综合征(MDS)和急性髓系白血病(AML)治疗的基石。口服制剂提供静脉(IV)给药的替代方案,但比较真实世界的毒性数据仍然有限。我们评估了口服与静脉注射HMAs相关的血液学毒性和不良事件。方法:我们在2016年1月1日至2023年6月1日期间,在三个学术癌症中心对33例口服地西他滨/cedazuridine或口服阿扎胞苷治疗的MDS或AML患者进行了多中心回顾性队列研究。20名同时接受静脉注射HMAs的患者被纳入患者内配对分析。通过绝对值和从基线到最低点的百分比变化来评估细胞减少。采用Wilcoxon符号秩检验进行患者内比较,描述性地记录临床显著不良事件。结果:在纳入的20例患者中,口服HMA治疗期间血红蛋白下降中位数为20.8%,静脉注射HMA治疗期间血红蛋白下降中位数为20.5%。绝对中性粒细胞计数下降的中位数分别为95.9%和97.3%,血小板计数下降的中位数分别为81.9%和88.6%。口服和静脉注射HMA治疗在血红蛋白(p = 0.60)、绝对中性粒细胞计数(p = 0.63)和血小板计数(p = 0.06)方面无统计学差异。60.6%的患者在口服HMA治疗期间住院,70.0%的患者在静脉注射HMA治疗期间住院,51.5%和60.0%的患者出现中性粒细胞减少症。结论:口服HMAs显示出细胞减少的严重程度和不良事件发生率与静脉注射HMAs相当,支持口服制剂作为MDS和AML患者的实用替代方案。虽然令人鼓舞,但这些发现应该在回顾性设计和适度样本量的背景下进行解释。
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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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