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慢性髓性白血病序贯酪氨酸激酶抑制剂治疗后的无事件生存情况。

Current event-free survival after sequential tyrosine kinase inhibitor therapy for chronic myeloid leukemia.

机构信息

Department of Leukemia, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Cancer. 2011 Jan 15;117(2):327-35. doi: 10.1002/cncr.25604. Epub 2010 Sep 15.

DOI:10.1002/cncr.25604
PMID:20845478
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4327987/
Abstract

BACKGROUND

Imatinib is an effective tyrosine kinase inhibitor (TKI) for patients with chronic myeloid leukemia (CML) in chronic phase (CP). Although some patients may fail on therapy with imatinib, effective salvage therapy is available with second-generation TKIs. Current measurement of efficacy for each therapy is judged by its individual impact on overall survival and event-free survival (EFS).

METHODS

In total, 586 patients with CML in CP who received imatinib were included in this analysis in 2 cohorts: imatinib as front-line therapy (n = 281) or after failure on interferon-α (IFN-α) (n = 305). By accounting for successful salvage treatment (ie, regain of complete cytogenetic response), the current EFS (CEFS) rate was calculated to obtain a more accurate impression of the outcome of patients with CML who received treatment with sequential TKIs.

RESULTS

For patients who received imatinib after failing on IFN-α, the 7-year EFS rate was 61%, whereas the CEFS rate was 69%. The 7-year EFS rate for patients who received imatinib as initial therapy was 81% compared with a 7-year CEFS rate of 88%.

CONCLUSIONS

CEFS provided a more accurate representation of the outcome of patients with CML in CP. These patients may frequently be treated successfully with subsequent TKIs after experiencing failure on the first TKI.

摘要

背景

伊马替尼是一种有效的酪氨酸激酶抑制剂(TKI),适用于慢性期(CP)慢性髓性白血病(CML)患者。尽管一些患者可能会对伊马替尼治疗产生耐药,但仍有有效的二线 TKI 治疗方案。目前,每种治疗方法的疗效评估均通过其对总生存(OS)和无事件生存(EFS)的个体影响来判断。

方法

本分析共纳入 586 例接受伊马替尼治疗的 CP 期 CML 患者,分为 2 个队列:一线治疗(n=281)或 IFN-α(IFN-α)治疗失败后(n=305)。通过对成功挽救治疗(即完全细胞遗传学缓解的恢复)进行核算,计算当前 EFS(CEFS)率,以更准确地评估接受序贯 TKI 治疗的 CML 患者的治疗结局。

结果

对于 IFN-α 治疗失败后接受伊马替尼治疗的患者,7 年 EFS 率为 61%,而 CEFS 率为 69%。一线治疗接受伊马替尼治疗的患者 7 年 EFS 率为 81%,而 7 年 CEFS 率为 88%。

结论

CEFS 更准确地反映了 CP 期 CML 患者的治疗结局。这些患者在一线 TKI 治疗失败后,常可通过后续 TKI 治疗成功治愈。

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本文引用的文献

1
Survival of patients with chronic myelocytic leukemia: comparisons of estimates from clinical trial settings and population-based cancer registries.慢性髓性白血病患者的生存情况:临床试验环境和基于人群的癌症登记处估计值的比较。
Oncologist. 2011;16(5):663-71. doi: 10.1634/theoncologist.2010-0393. Epub 2011 Apr 6.
2
Phase III, randomized, open-label study of daily imatinib mesylate 400 mg versus 800 mg in patients with newly diagnosed, previously untreated chronic myeloid leukemia in chronic phase using molecular end points: tyrosine kinase inhibitor optimization and selectivity study.采用分子终点的新诊断、未经治疗的慢性期慢性髓性白血病患者每日甲磺酸伊马替尼 400mg 与 800mg 的随机、开放标签 III 期研究:酪氨酸激酶抑制剂优化和选择性研究。
J Clin Oncol. 2010 Jan 20;28(3):424-30. doi: 10.1200/JCO.2009.25.3724. Epub 2009 Dec 14.
3
Chronic myeloid leukemia: sequencing of TKI therapies.
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Hematology Am Soc Hematol Educ Program. 2016 Dec 2;2016(1):164-169. doi: 10.1182/asheducation-2016.1.164.
4
Long-term molecular and cytogenetic response and survival outcomes with imatinib 400 mg, imatinib 800 mg, dasatinib, and nilotinib in patients with chronic-phase chronic myeloid leukaemia: retrospective analysis of patient data from five clinical trials.伊马替尼400mg、伊马替尼800mg、达沙替尼和尼洛替尼用于慢性期慢性髓性白血病患者的长期分子和细胞遗传学反应及生存结果:来自五项临床试验患者数据的回顾性分析
Lancet Haematol. 2015 Mar;2(3):e118-28. doi: 10.1016/S2352-3026(15)00021-6. Epub 2015 Mar 20.
5
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6
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7
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8
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9
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10
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Blood. 2009 Dec 3;114(24):4933-8. doi: 10.1182/blood-2009-07-232595. Epub 2009 Oct 12.
4
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J Clin Oncol. 2009 Oct 1;27(28):4754-9. doi: 10.1200/JCO.2008.20.3869. Epub 2009 Aug 31.
5
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6
Delayed achievement of cytogenetic and molecular response is associated with increased risk of progression among patients with chronic myeloid leukemia in early chronic phase receiving high-dose or standard-dose imatinib therapy.在接受高剂量或标准剂量伊马替尼治疗的慢性髓性白血病慢性期早期患者中,细胞遗传学和分子反应延迟实现与疾病进展风险增加相关。
Blood. 2009 Jun 18;113(25):6315-21. doi: 10.1182/blood-2008-07-166694. Epub 2009 Apr 15.
7
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Blood. 2009 May 7;113(19):4497-504. doi: 10.1182/blood-2008-12-191254. Epub 2009 Mar 4.
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Blood. 2009 Apr 9;113(15):3428-34. doi: 10.1182/blood-2007-08-103499. Epub 2009 Feb 11.
9
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Blood. 2008 Nov 15;112(10):3965-73. doi: 10.1182/blood-2008-06-161737. Epub 2008 Sep 3.
10
Intermittent target inhibition with dasatinib 100 mg once daily preserves efficacy and improves tolerability in imatinib-resistant and -intolerant chronic-phase chronic myeloid leukemia.每日一次服用100毫克达沙替尼进行间歇性靶向抑制可维持疗效,并提高对伊马替尼耐药和不耐受的慢性期慢性髓性白血病患者的耐受性。
J Clin Oncol. 2008 Jul 1;26(19):3204-12. doi: 10.1200/JCO.2007.14.9260. Epub 2008 Jun 9.