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Clinical Study on Second-generation Tyrosine Kinase Inhibitors in the First-line |and Second-line Treatment of Chronic Myeloid Leukemia |
CHEN Heng, JIANG Yuanqiang, SHEN Yunfeng, et al |
The People's Hospital of Wuxi, Jiangsu Wuxi 214000, China |
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Abstract Objective: To investigate the clinical effect of second-generation tyrosine kinase inhibitors in the treatment of chronic myeloid leukemia (CML). Methods: A total of 64 patients with CML treated between January 2013 and December 2016 were selected as study subjects and treated with second-generation tyrosine kinase inhibitor (TKI). Among them, there were 41 cases treated with Nilotinib and 23 cases with Dasatinib. In patients treated by TKI, there were 13 cases receiving first-line medication and 51 cases receiving second-line medication. All were followed up for 6 ~ 54 months, median 18 months. The overall complete hematologic remission (CHR) rate, CCyR rate, rate of major cytogenetic response (MCyR), MMR rate, follow-up overall survival rate (OS) and event free survival rate (EFS) were observed; Meanwhile, the responses of first-line and second-line treatment and adverse drug reactions were compared. Results: At the end of follow-up, 43 cases continued second-generation TKI treatment, 14 cases died, 2 cases stopped medication, 2 cases were lost to follow up and 3 cases changed the medication regimen; In terms of overall responses to treatment, the rates of CHR, MCyR, CCyR and MMR were 98.44%, 64.00%, 59.37% and 43.75% respectively; In terms of overall survival status, OS and EFS decreased with duration of the disease. The rates of CCyR, MCyR and MMR of first-line treatment were significantly higher than the second-line treatment (P < 0.05); There were no significant differences in the incidence of adverse drug reactions between Nilotinib and Dasatinib (P > 0.05). Conclusion: The effect of Nilotinib and Dasatinib second-generation TKI in the treatment of CML is clear. The prognosis is good and safety is better; The effect of second generation TKI first-line treatment is better than second-line treatment in treating CML.
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[1]杨剑岭,曹晓正,何丽华,等.5,7-二甲氧基黄酮对K562细胞凋亡和livin基因表达的影响[J].湖南师范大学学报(医学版),2013,10(4):16~18. [2] 高玉萍,董平,刘永,等.WT1、VEGF基因在急性白血病患者外周血中的表达及其意义[J].医学临床研究,2015,32(12):2454~2456. [3] 刘瑜,曾艳,彭翠翠,等.急性白血病行自体外周血造血干细胞移植治疗的临床疗效分析[J].成都医学院学报,2016,11(2):201~205. [4] 江倩,赵东陆,金洁,等.国产甲磺酸伊马替尼治疗慢性髓性白血病慢性期早期疗效和安全性的前瞻性、多中心临床研究[J].中华血液学杂志,2015,36(8):651~655. [5] 李丹露,李希娜,杨丽杰,等.甲磺酸伊马替尼治疗慢性髓细胞白血病的不良反应和防治措施[J].中国药物警戒,2013,10(8):486~487,491. [6] 中华医学会血液学分会实验诊断学组,中国慢性髓性白血病联盟专家组.中国慢性髓性白血病诊疗监测规范(2014年版)[J].中华血液学杂志,2014,35(8):781~784. [7] 孔佩艳,曾东风,李杰平,等.老年急性髓细胞白血病临床和治疗的特殊问题[J].西部医学,2012,24(11):2047~2048. [8] 牧启田,陈志妹,楼基余,等.酪氨酸激酶抑制剂治疗后慢性髓细胞白血病患者Ph阴性细胞中染色体异常的遗传学特征和转归[J].中华医学遗传学杂志,2012,29(1):64~67. [9] 吕素娟,朱焕玲,李向龙,等.二代酪氨酸激酶抑制剂治疗慢性髓细胞白血病临床疗效分析[J].四川大学学报(医学版),2016,47(2):287~291. [10] 胡学茜,马爱霞.达沙替尼和尼洛替尼一线治疗初诊慢性髓性白血病慢性期的临床研究进展[J].中国药房,2015,26(14):2007~2010. |
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