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甲磺酸伊马替尼停药用于一线甲磺酸伊马替尼治疗且达到完全分子学缓解的慢性髓性白血病患者。

Imatinib mesylate discontinuation in patients with chronic myeloid leukemia who have received front-line imatinib mesylate therapy and achieved complete molecular response.

机构信息

Division of Hematology/Oncology, Department of Internal Medicine, Chonbuk National University Medical School, Deokjin-gu, Jeonju, Republic of Korea.

出版信息

Leuk Res. 2012 Jun;36(6):689-93. doi: 10.1016/j.leukres.2012.02.011. Epub 2012 Mar 5.

Abstract

The aims were to investigate the feasibility of imatinib mesylate (IM) discontinuation in chronic myeloid leukemia patients who were initially treated with IM and achieved complete molecular response (CMR). Fourteen patients were included. Ten were relapsed within 9.5 months after discontinuation of IM. All 7 patients with high Sokal risk were relapsed. The probability of CMR persistence at 1-year was 28.6%. All relapsed patients were still responsive to IM. A high Sokal risk and delayed acquisition of CMR were associated with relapse. IM discontinuation in patients achieved CMR after treatment with front-line IM might be feasible. Further studies are warranted.

摘要

目的在于研究伊马替尼甲磺酸盐(IM)在初始接受 IM 治疗并达到完全分子反应(CMR)的慢性髓性白血病患者中停药的可行性。共纳入 14 例患者,其中 10 例在 IM 停药后 9.5 个月内复发,所有 7 例高 Sokal 风险的患者均复发。CMR 持续 1 年的概率为 28.6%。所有复发患者对 IM 仍有反应。高 Sokal 风险和 CMR 延迟获得与复发相关。一线 IM 治疗后达到 CMR 的患者停用 IM 可能是可行的。需要进一步研究。

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