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首页> 外文期刊>Revista Brasileira de Hematologia e Hemoterapia >Molecular response to imatinib mesylate of Brazilian patients with chronic myeloid leukemia
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Molecular response to imatinib mesylate of Brazilian patients with chronic myeloid leukemia

机译:巴西慢性粒细胞白血病患者对甲磺酸伊马替尼的分子反应

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Background Imatinib mesylate has revolutionized the treatment of chronic myeloid leukemia leading to significant reductions of BCR-ABL1 transcript levels in peripheral blood. Objective To evaluate the response to imatinib mesylate treatment (400 mg/day) in Brazilian patients in the chronic phase of chronic myeloid leukemia monitored by quantitative real time polymerase chain reaction. Methods Between October 2002 and October 2010, 3169 peripheral blood samples were collected from 1403 patients from 3 to 5 months, 6 to 11 months, 12 to 17 months, 18 to 23 months and a?¥24 months after beginning imatinib treatment. Eighty-two patients had samples available and analyzed for all time intervals. BCR-ABL1 quantification was performed by quantitative real time polymerase chain reaction using the ABL1 gene as the control. Results of the BCR-ABL1 ratio as a percentage were reported by the international scale (IS) using the laboratory conversion factor (0.51). Results In the first interval, 80.8% of patients achieved the optimal response ( BCR-ABL1 IS a?¤ 10%). In the second period, 69.1% achieved optimal response ( BCR-ABL1 IS a?¤ 1%) and, between 12 and 17 months, 47.3% achieved major molecular response ( BCR-ABL1 IS a?¤ 0.1%). Conclusions The results of this retrospective study show that the response to imatinib treatment (400 mg/day) of Brazilian patients in the chronic phase of chronic myeloid leukemia is within the expected profile when compared to patients reported in international prospective randomized studies.
机译:背景甲磺酸伊马替尼彻底改变了慢性粒细胞白血病的治疗方法,导致外周血BCR-ABL1转录水平显着降低。目的通过定量实时聚合酶链反应监测在慢性粒细胞白血病慢性期巴西患者对甲磺酸伊马替尼治疗(400 mg /天)的反应。方法2002年10月至2010年10月,在开始伊马替尼治疗后3到5个月,6到11个月,12到17个月,18到23个月和24个月的时间,从1403名患者中收集了3169份外周血样本。 82位患者有可用样本并在所有时间间隔内进行了分析。使用ABL1基因作为对照,通过定量实时聚合酶链反应进行BCR-ABL1定量。 BCR-ABL1比值的结果以国际换算(IS)的实验室换算系数(0.51)报告。结果在第一个间隔中,有80.8%的患者达到了最佳反应(BCR-ABL1 IS约为10%)。在第二阶段,有69.1%的患者获得了最佳的反应(BCR-ABL1为1%),而在12到17个月之间,有47.3%的患者获得了主要的分子反应(BCR-ABL1为0.1%)。结论这项回顾性研究的结果表明,与国际前瞻性随机研究中报道的患者相比,巴西慢性粒细胞白血病慢性期患者对伊马替尼治疗(400 mg /天)的反应在预期范围内。

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