Suppr超能文献

甲磺酸伊马替尼治疗慢性髓性白血病早期和晚期慢性期的长期疗效、细胞遗传学和分子学反应评价:单中心报告。

Evaluation of long-term outcomes, cytogenetic and molecular responses with imatinib mesylate in early and late chronic-phase chronic myeloid leukemia: a report from a single institute.

机构信息

Tumor Biology Laboratory, University of São Paulo, São Paulo, Brazil.

出版信息

Acta Haematol. 2012;128(4):223-32. doi: 10.1159/000339696. Epub 2012 Aug 22.

Abstract

Here we compare the management and survival outcomes of chronic myeloid leukemia (CML) patients who had early or late imatinib mesylate (IM) therapy. The cytogenetic and molecular responses of 189 CML patients were analyzed. Of this group, 121 patients were classified as the early chronic phase (ECP) group and started IM within 12 months of diagnosis. The other 68 patients were classified as the late chronic phase (LCP) group who had been treated with interferon (IFN)-alpha-2 and crossed over to IM more than 12 months after diagnosis. The overall rates of complete cytogenetic response (CCyR) and major molecular response (MMR) at last follow-up were 83.6 and 78.1% in the ECP and LCP groups, respectively. The CCyR rates were 89.3 (for ECP patients) versus 73.5% (for LCP patients; p < 0.0001). At last follow-up, 82.4% ECP and 64.2% LCP patients had achieved an MMR (p < 0.0001). No significant differences were noted between the two groups with regard to survival outcomes. Our experience reveals that IM is an effective rescue therapy in most CML LCP patients who are intolerant or in whom IFN-alpha therapy fails. Such therapeutic options should be considered in LCP patients, particularly in countries where IM may not be available.

摘要

在这里,我们比较了接受早期或晚期甲磺酸伊马替尼(IM)治疗的慢性髓性白血病(CML)患者的治疗管理和生存结局。分析了 189 例 CML 患者的细胞遗传学和分子反应。在这组患者中,121 例被分类为早期慢性期(ECP)组,在诊断后 12 个月内开始接受 IM 治疗。另 68 例被分类为晚期慢性期(LCP)组,在诊断后超过 12 个月接受干扰素(IFN)-α-2 治疗并转为 IM 治疗。在最后一次随访时,ECP 和 LCP 组的完全细胞遗传学缓解(CCyR)和主要分子缓解(MMR)的总体率分别为 83.6%和 78.1%。CCyR 率分别为 89.3%(ECP 患者)和 73.5%(LCP 患者;p<0.0001)。在最后一次随访时,82.4%的 ECP 和 64.2%的 LCP 患者达到了 MMR(p<0.0001)。两组患者的生存结局无显著差异。我们的经验表明,对于不耐受或 IFN-α 治疗失败的大多数 CML LCP 患者,IM 是一种有效的挽救治疗。对于 LCP 患者,特别是在无法获得 IM 的国家,应考虑这种治疗选择。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验