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首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Very long-term follow-up results of imatinib mesylate therapy in chronic phase chronic myeloid leukemia after failure of interferon alpha therapy
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Very long-term follow-up results of imatinib mesylate therapy in chronic phase chronic myeloid leukemia after failure of interferon alpha therapy

机译:甲磺酸伊马替尼治疗干扰素α治疗失败后慢性阶段慢性粒细胞白血病的非常长期随访结果

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BACKGROUND: The long-term outcome of patients with chronic phase chronic myeloid leukemia treated with imatinib after failure of interferon alpha therapy has not been detailed. METHODS: In total, 368 patients were analyzed. Univariate and multivariate survival analyses were conducted using standard statistical methods. RESULTS: Overall, 247 patients (67%) achieved a complete cytogenetic response (CCyR). Of the 327 patients who were studied, 207 patients (63%) achieved a major molecular response (MMR), and 99 patients (30%) had undetectable breakpoint cluster region/c-abl oncogene (BCR-ABL) levels at some time during therapy. The estimated 10-year survival rate was 68%, the progression-free survival rate was 67%, and the event-free survival rate was 51%. In multivariate analysis, age ≥60 years, hemoglobin <10 g/dL, bone marrow basophils ≥5%, any peripheral blasts, and clonal evolution were independent adverse factors for survival. The estimated 7-year survival rate according to the presence of no factors (n = 154), 1 or 2 factors (n = 190), or ≥3 factors (n = 24) were 93%, 70%, and 25%, respectively (P < .01). Achieving an MMR, a CCyR, or a partial cytogenetic response at 12 months was associated with significantly better 10-year survival rate in a landmark analysis (10-year survival rate, 80%-90%) compared with achieving a minor cytogenetic response or a complete hematologic response (10-year survival rate, 55%-65%) or another response (10-year survival rate, 10%). In a landmark analysis that included imatinib response at 12 months, achieving a major cytogenetic response or better (hazard ratio, 0.12; P < .001) and achieving a complete hematologic response or a minor cytogenetic response (hazard ratio, 0.36; P = .003) were significant favorable prognostic factors. CONCLUSIONS: The current results indicated that the estimated 10-year survival rate of 68% for patients with chronic myeloid leukemia who receive imatinib after failure on interferon has improved.
机译:背景:α-干扰素治疗失败后,使用伊马替尼治疗的慢性期慢性粒细胞白血病患者的长期预后尚未阐明。方法:总共分析了368例患者。使用标准统计方法进行单因素和多因素生存分析。结果:总体上,247例患者(67%)实现了完全的细胞遗传学应答(CCyR)。在研究的327位患者中,有207位患者(63%)达到了主要分子反应(MMR),而99位患者(30%)在此期间的某个时间段检测不到断点簇区域/ c-abl癌基因(BCR-ABL)水平治疗。估计的10年生存率为68%,无进展生存率为67%,无事件生存率为51%。在多因素分析中,年龄≥60岁,血红蛋白<10 g / dL,骨髓嗜碱性粒细胞≥5%,任何外周母细胞和克隆进化是生存的独立不利因素。根据无因素(n = 154),1个或2个因素(n = 190)或≥3个因素(n = 24)的存在,估计的7年生存率分别为93%,70%和25%, (P <.01)。在12个月时达到MMR,CCyR或部分细胞遗传学反应与里程碑式分析相比,与实现较小的细胞遗传学反应或获得显着改善的10年生存率(10年生存率80%-90%)相关,或者完全血液学反应(10年生存率,55%-65%)或其他反应(10年生存率,10%)。在一项具有里程碑意义的分析中,包括伊马替尼在12个月时的反应,达到主要的细胞遗传学反应或更好(危险比,0.12; P <.001)并达到完全的血液学反应或次要的细胞遗传学反应(危险比,0.36; P =。 003)是重要的有利预后因素。结论:目前的结果表明,干扰素治疗失败后接受伊马替尼治疗的慢性粒细胞白血病患者的10年生存率估计为68%。

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