Decitabine Versus Intensive Chemotherapy for Elderly Patients With Newly Diagnosed Acute Myeloid Leukemia

被引:5
作者
Choi, Eun-Ji [1 ]
Lee, Je-Hwan [1 ]
Park, Han-Seung [1 ]
Lee, Jung-Hee [1 ]
Seol, Miee [1 ]
Lee, Young-Shin [1 ]
Kang, Young-Ah [1 ]
Jeon, Mijin [1 ]
Woo, Ji Min [1 ]
Lee, Kyoo-Hyung [1 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Hematol, 88,Olymp Ro 43 Gil, Seoul 05505, South Korea
基金
新加坡国家研究基金会;
关键词
Acute myeloid leukemia; Decitabine; Elderly; Hypomethylating agent; Intensive chemotherapy; RISK MYELODYSPLASTIC SYNDROMES; OLDER PATIENTS; EPIGENETIC THERAPY; SCORING SYSTEM; OPEN-LABEL; GENE; AZACITIDINE; METHYLATION; SURVIVAL; MDS;
D O I
10.1016/j.clml.2019.02.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The outcome of elderly patients with acute myeloid leukemia (AML) has generally been poor, and therapeutic decisions are often challenging. We compared conventional intensive chemotherapy (IC) versus decitabine, which showed potential for elderly patients with AML. Decitabine showed a lower response rate but similar survival outcomes compared with IC. In a subgroup analysis, some patients with specific genetic abnormalities benefited from each treatment option. Background: Elderly patients with acute myeloid leukemia (AML) have generally had a poor prognosis with unfavorable clinical and biologic disease features. Hypomethylating agents have shown potential for treating medically unfit and elderly patients with AML. Patients and Methods: We compared the outcomes of elderly patients with AML treated with decitabine and intensive chemotherapy (IC). Results: The data from 107 patients with newly diagnosed AML aged >= 65 years were analyzed. The overall response rate was 38.6% and was significantly greater in the IC group than in the decitabine group (65.6% vs. 26.1%; P < .001). With a median follow-up duration of survivors of 14.8 months, the median overall survival (OS) and event-free survival were 12.3 months (95% confidence interval [CI], 10.0-14.7) and 2.0 months (95% CI, 2.0-2.0), respectively, which were not different between the 2 treatment groups. The FLT3-internal tandem duplication mutation (hazard ratio [HR], 2.637; 95% CI, 1.379-5.043; P = .003), complex karyotype (HR, 2.513; 95% CI, 1.258-5.020; P = .009), and peripheral blood blast percentage at diagnosis (HR, 1.983; 95% CI, 1.148-3.422; P = .014) were analyzed as independent prognostic factors for OS. A subgroup analysis for OS showed that IC was superior to decitabine for patients with the FLT3-internal tandem duplication mutation (P = .025) and poor risk cytogenetics, except for -7/del(7q) (P = .005), and decitabine was associated with longer OS for patients with -7/del(7q) (P = .077). Conclusion: Decitabine showed a similar OS to IC, despite the lower response rate in patients. The clinical outcomes of specific subgroups seemed to differ with different treatment options. Optimal therapeutic approaches for elderly patients with AML should be further examined.
引用
收藏
页码:290 / +
页数:13
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