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首页> 外文期刊>International journal of hematology >Treatment outcomes of chronic-phase chronic myeloid leukemia with resistance and/or intolerance to a 1st-line tyrosine kinase inhibitor in Japan: the results of the New TARGET study 2nd-line
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Treatment outcomes of chronic-phase chronic myeloid leukemia with resistance and/or intolerance to a 1st-line tyrosine kinase inhibitor in Japan: the results of the New TARGET study 2nd-line

机译:慢性相慢性髓性白血病对日本第一线酪氨酸激酶抑制剂的耐药性和/或不耐受的治疗结果:新目标研究的结果2ND-LINE

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摘要

We herein report the results of the New TARGET study 2nd-line, which collected data on patients with chronic-phase (CP) chronic myeloid leukemia (CML) who received a 2nd-line tyrosine kinase inhibitor (TKI) because of resistance and/or to a 1st-line TKI. A total of 98 patients were enrolled intolerance between April 2010 and March 2013, and 82 patients were analyzed. The median age was 54 years (range 22-88 years). Seventy-six patients (93%) received imatinib as the 1st-line TKI. Forty-five (55%) and 37 (45%) patients began nilotinib and dasatinib treatments at entry, respectively. First-line TKI treatment achieved complete hematological response in 79 patients (96%) and complete cytogenetic response (CCyR) in 49 patients (60%), respectively. Nine patients (11%) had BCR-ABL1 kinase domain point mutations at enrollment. The estimated 3-year progression-free-survival rate after enrollment was 98.7% (95% CI 91.1-99.8%). Overall, the probabilities of achieving CCyR and a major molecular response were 89.3% (95% CI 81.4-94.8%) and 87.2% (95% CI 78.1-93.8%), respectively. There were no new safety issues. This study demonstrated that CML-CP patients in Japan who are resistant and/or intolerant to a 1st-line TKI can achieve an extremely good outcome by 2nd-line TKI treatment.
机译:我们在此报告了新的目标研究2nd-line的结果,其收集了对慢性阶段(CP)慢性骨髓性白血病(CML)的患者的数据,因为抗性和/或到1号TKI。共有98名患者于2010年4月至2013年3月期间注册了不耐受,分析了82名患者。中位年龄为54岁(范围22-88岁)。七十六名患者(93%)将伊马替尼接受为第一线TKI。四十五(55%)和37名(45%)患者分别开始尼洛替尼和达斯替尼治疗。第一线TKI治疗分别在49名患者(96%)(96%)和完全细胞遗传学反应(CCYR)中达到完全血液应答(60%)。九名患者(11%)在注册时具有BCR-ABL1激酶域点突变。估计征收估计的3年患儿的存活率为98.7%(95%CI 91.1-99.8%)。总体而言,实现CCγR的概率和主要分子反应的概率分别为89.3%(95%CI 81.4-94.8%)和87.2%(95%CI 78.1-93.8%)。没有新的安全问题。本研究表明,日本的CML-CP患者耐药和/或不耐受1线TKI的患者可以通过2nd-LINE TKI治疗来实现极好的结果。

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