Molecular response to imatinib mesylate of Brazilian patients with chronic myeloid leukemia

Ana Lucia Vieira-Mion, Noemi Farah Pereira, Vaneuza Araujo Moreira Funke, Ricardo Pasquini
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引用次数: 8

Abstract

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 ≥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-ABL1IS  10%). In the second period, 69.1% achieved optimal response (BCR-ABL1IS  1%) and, between 12 and 17 months, 47.3% achieved major molecular response (BCR-ABL1IS  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.

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巴西慢性髓性白血病患者对甲磺酸伊马替尼的分子反应
甲磺酸地马替尼已经彻底改变了慢性髓性白血病的治疗,导致外周血中BCR-ABL1转录物水平显著降低。目的用实时定量聚合酶链反应监测巴西慢性髓系白血病慢行期患者对甲磺酸伊马替尼(400mg /d)治疗的反应。方法2002年10月至2010年10月,收集1403例患者外周血样本3169份,时间分别为开始伊马替尼治疗后3 ~ 5个月、6 ~ 11个月、12 ~ 17个月、18 ~ 23个月和≥24个月。82名患者有可用的样本,并在所有时间间隔内进行分析。以ABL1基因为对照,采用实时定量聚合酶链反应进行BCR-ABL1定量。BCR-ABL1比率作为百分比的结果由国际比例尺(IS)报告,使用实验室转换因子(0.51)。结果在第一期,80.8%的患者获得最佳缓解(BCR-ABL1IS≤10%)。在第二阶段,69.1%的患者获得最佳缓解(BCR-ABL1IS≤1%),在12 - 17个月期间,47.3%的患者获得主要分子缓解(BCR-ABL1IS≤0.1%)。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,巴西慢性髓性白血病慢性期患者对伊马替尼治疗(400mg /天)的反应在预期范围内。
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来源期刊
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审稿时长
21 weeks
期刊介绍: A Revista Brasileira de Hematologia e Hemoterapia é um periódico científico de propriedade da Associação Brasileira de Hematologia e Hemoterapia, publicada bimestralmente. A abreviatura de seu título é Rev. Bras. Hematol. Hemoter., que deve ser usada em bibliografias, notas de rodapé e em referências e legendas bibliográficas.
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