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甲磺酸伊马替尼停药后慢性髓性白血病患者微小残留病检测不到的长期预后

Long-Term Outcomes after Imatinib Mesylate Discontinuation in Chronic Myeloid Leukemia Patients with Undetectable Minimal Residual Disease.

作者信息

Yhim Ho-Young, Lee Na-Ri, Song Eun-Kee, Yim Chang-Yeol, Jeon So Yeon, Lee Bohee, Kim Jeong-A, Kim Hee Sun, Cho Eun Hae, Kwak Jae-Yong

机构信息

Department of Internal Medicine, Chonbuk National University Medical School, Jeonju, Republic of Korea.

出版信息

Acta Haematol. 2016;135(3):133-9. doi: 10.1159/000440936. Epub 2015 Nov 5.

DOI:10.1159/000440936
PMID:26535871
Abstract

BACKGROUND

Imatinib mesylate (IM) discontinuation is under active investigation in chronic myeloid leukemia-chronic phase (CML-CP) patients with undetectable minimal residual disease (UMRD). However, limited data exist on the long-term outcomes following IM discontinuation in patients treated with frontline IM therapy.

METHODS

We consecutively enrolled patients with CML-CP who discontinued IM after achieving UMRD for ≥12 months between June 2009 and January 2013.

RESULTS

Nineteen patients (8 male, 11 female) were included. After IM discontinuation, 14 patients (74%) lost UMRD after a median of 4.0 months. Of the 14 patients with molecular relapses, 12 (86%) relapsed within the first 9 months after IM discontinuation and 2 (14%) relapsed at 20.5 and 22.8 months, respectively. No molecular relapse was observed after 2 years of IM discontinuation. With a median follow-up of 58.1 months (range 23.0-66.5), the estimated UMRD persistence rate at 5 years was 23.7%. IM was readministered in all patients with molecular relapse, and 12 patients (86%) reachieved UMRD at a median of 5.3 months. A high-risk Sokal score, delayed UMRD achievement and short-term IM therapy were significantly associated with molecular relapse.

CONCLUSION

These findings suggest that IM discontinuation in patients who achieved UMRD after frontline IM therapy resulted in favorable long-term outcomes in terms of safety and feasibility.

摘要

背景

对于微小残留病不可检测(UMRD)的慢性髓性白血病慢性期(CML-CP)患者,甲磺酸伊马替尼(IM)停药正在积极研究中。然而,关于一线IM治疗患者停药后的长期结局的数据有限。

方法

我们连续纳入了2009年6月至2013年1月期间在达到UMRD≥12个月后停用IM的CML-CP患者。

结果

纳入19例患者(8例男性,11例女性)。IM停药后,14例患者(74%)在中位4.0个月后失去UMRD。在14例分子复发的患者中,12例(86%)在IM停药后的前9个月内复发,2例(14%)分别在20.5个月和22.8个月复发。IM停药2年后未观察到分子复发。中位随访58.1个月(范围23.0 - 66.5个月),5年时估计的UMRD持续率为23.7%。所有分子复发的患者均重新给予IM治疗,12例患者(86%)在中位5.3个月时再次达到UMRD。高危Sokal评分、UMRD获得延迟和短期IM治疗与分子复发显著相关。

结论

这些发现表明,一线IM治疗后达到UMRD的患者停药在安全性和可行性方面产生了良好的长期结局。

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