Superior outcome with hypomethylating therapy in patients with acute myeloid leukemia and high-risk myelodysplastic syndrome and chromosome 5 and 7 abnormalities.

Superior outcome with hypomethylating therapy in patients with acute myeloid leukemia and high-risk myelodysplastic syndrome and chromosome 5 and 7 abnormalities.
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DOI:
10.1002/cncr.24661
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发表时间:
2009-12-15
期刊:
影响因子:
6.2
通讯作者:
Kantarjian, Hagop
Kantarjian, Hagop
中科院分区:
医学1区
文献类型:
--
作者:
Ravandi, Farhad;Issa, Jean-Pierre;Garcia-Manero, Guillermo;O'Brien, Susan;Pierce, Sherry;Shan, Jianqin;Borthakur, Gautam;Verstovsek, Srdan;Faderl, Stefan;Cortes, Jorge;Kantarjian, Hagop

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伴有5号和7号染色体异常的急性髓性白血病(AML)和高危骨髓增生异常综合征(MDS)患者[不包括del 5(q)]的预后很差,不到10%的患者在2年时存活。我们调查了使用低甲基化药物(5-氮杂胞苷/地西他滨)治疗是否能改善结果。2004年1月至2007年12月,81例患者[37例(46%)急性髓性白血病(≥20%);44例(54%)5号和7号染色体异常的高危MDS患者以低甲基化药物作为初始治疗。其中包括68例复杂(≥3)异常患者和13例少于3例异常患者。同期,151例5号和7号染色体异常患者(126例AML, 25例MDS)(128例复杂,23例非复杂)接受了强化化疗(包括72%的阿糖胞苷为基础的方案,28%的其他方案)。两组患者的中位年龄分别为66岁和61岁[范围(37-85)和(19-89)]。低甲基化组33例(41%)患者达到CR,化疗组53例(35%)患者达到CR (p=0.395)。中位随访时间为51周(12 - 101周)和40周(5-128周),低甲基化组22/33例患者和化疗组33/53例患者复发。中位CR持续时间分别为45周和23周(p=0.153)。低甲基化组的总生存期优于化疗组(p=0.019)。对于5号和7号染色体异常的患者,使用低甲基化药物治疗可能优于化疗。
Outcome of patients with acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS) with chromosome 5 and 7 abnormalities [excluding del 5(q)] has been poor with fewer than 10% of patients alive at 2 years. We investigated whether treatment with hypomethylating agents (5-azacytidine/decitabine) leads to an improved outcome. Between January 2004 and December 2007, 81 patients [37 (46%) with AML (≥ 20% blast); 44 (54%) with high-risk MDS] with chromosome 5 and 7 abnormalities were treated with hypomethylating agents as their initial therapy. These included 68 patients with complex (≥ 3) abnormalities and 13 with less than 3 aberrations. During the same period, 151 patients (126 with AML, 25 with MDS) with chromosome 5 and 7 abnormalities (128 complex, 23 non-complex) were treated with intensive chemotherapy (including cytarabine based regimens in 72% and other in 28%). Median ages for the two groups were 66 and 61 years, respectively [(ranges (37–85) and (19–89)]. Thirty three (41%) patients in the hypomethylating group achieved CR versus 53 (35%) in the chemotherapy group (p=0.395). With a median follow up of 51 weeks (range 12 – 101) and 40 weeks (range, 5–128), 22/33 patients in the hypomethylating group and 33/53 patients in the chemotherapy group have relapsed. The median CR duration was 45 weeks and 23 weeks, respectively (p=0.153). The overall survival was superior for the hypomethylating group compared to the chemotherapy group (p=0.019). Treatment with hypomethylating agents may be superior to chemotherapy in patients with chromosome 5 and 7 abnormalities.
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