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2
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Assessment of BCR-ABL1 transcript levels at 3 months is the only requirement for predicting outcome for patients with chronic myeloid leukemia treated with tyrosine kinase inhibitors.评估慢性髓性白血病患者接受酪氨酸激酶抑制剂治疗 3 个月时的 BCR-ABL1 转录本水平是预测其预后的唯一要求。
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Long-term outcome of patients with chronic myeloid leukemia treated with second-generation tyrosine kinase inhibitors after imatinib failure is predicted by the in vitro sensitivity of BCR-ABL kinase domain mutations.伊马替尼治疗失败后接受第二代酪氨酸激酶抑制剂治疗的慢性髓性白血病患者的长期预后可通过BCR-ABL激酶结构域突变的体外敏感性来预测。
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[Prognostic significance of early molecular response after second-line treatment with dasatinib of chronic myeloid leukemia patients].[达沙替尼二线治疗慢性髓性白血病患者后早期分子反应的预后意义]
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本文引用的文献

1
Assessment of BCR-ABL1 transcript levels at 3 months is the only requirement for predicting outcome for patients with chronic myeloid leukemia treated with tyrosine kinase inhibitors.评估慢性髓性白血病患者接受酪氨酸激酶抑制剂治疗 3 个月时的 BCR-ABL1 转录本水平是预测其预后的唯一要求。
J Clin Oncol. 2012 Jan 20;30(3):232-8. doi: 10.1200/JCO.2011.38.6565. Epub 2011 Nov 7.
2
Safety and efficacy of bosutinib (SKI-606) in chronic phase Philadelphia chromosome-positive chronic myeloid leukemia patients with resistance or intolerance to imatinib.博舒替尼(SKI-606)治疗对伊马替尼耐药或不耐受的慢性期费城染色体阳性慢性髓性白血病患者的安全性和疗效。
Blood. 2011 Oct 27;118(17):4567-76. doi: 10.1182/blood-2011-05-355594. Epub 2011 Aug 24.
3
Expanding Nilotinib Access in Clinical Trials (ENACT): an open-label, multicenter study of oral nilotinib in adult patients with imatinib-resistant or imatinib-intolerant Philadelphia chromosome-positive chronic myeloid leukemia in the chronic phase.扩大尼洛替尼在临床试验中的应用(ENACT):一项开放性、多中心研究,评估尼洛替尼治疗慢性期费城染色体阳性、伊马替尼耐药或不耐受的慢性髓性白血病成人患者的疗效。
Cancer. 2012 Jan 1;118(1):118-26. doi: 10.1002/cncr.26249. Epub 2011 Jul 5.
4
Nilotinib is effective in patients with chronic myeloid leukemia in chronic phase after imatinib resistance or intolerance: 24-month follow-up results.尼洛替尼治疗伊马替尼耐药或不耐受的慢性期慢性髓性白血病患者有效:24 个月随访结果。
Blood. 2011 Jan 27;117(4):1141-5. doi: 10.1182/blood-2010-03-277152. Epub 2010 Nov 22.
5
Predictive factors for outcome and response in patients treated with second-generation tyrosine kinase inhibitors for chronic myeloid leukemia in chronic phase after imatinib failure.伊马替尼治疗失败的慢性期慢性髓性白血病患者使用第二代酪氨酸激酶抑制剂治疗的预后和反应的预测因素。
Blood. 2011 Feb 10;117(6):1822-7. doi: 10.1182/blood-2010-07-293977. Epub 2010 Oct 28.
6
Efficacy of tyrosine kinase inhibitors (TKIs) as third-line therapy in patients with chronic myeloid leukemia in chronic phase who have failed 2 prior lines of TKI therapy.酪氨酸激酶抑制剂(TKIs)作为三线治疗在慢性期慢性髓性白血病患者中的疗效,这些患者在接受 2 线 TKI 治疗失败后。
Blood. 2010 Dec 16;116(25):5497-500. doi: 10.1182/blood-2010-06-291922. Epub 2010 Sep 10.
7
Potent, transient inhibition of BCR-ABL with dasatinib 100 mg daily achieves rapid and durable cytogenetic responses and high transformation-free survival rates in chronic phase chronic myeloid leukemia patients with resistance, suboptimal response or intolerance to imatinib.达沙替尼 100mg 每日治疗可强效、短暂地抑制 BCR-ABL,对于对伊马替尼耐药、治疗反应欠佳或不耐受的慢性期慢性髓性白血病患者,可迅速并持久地获得细胞遗传学反应,且无进展生存率较高。
Haematologica. 2010 Feb;95(2):232-40. doi: 10.3324/haematol.2009.011452.
8
Chronic myeloid leukemia: an update of concepts and management recommendations of European LeukemiaNet.慢性髓性白血病:欧洲白血病网络概念与管理建议的更新
J Clin Oncol. 2009 Dec 10;27(35):6041-51. doi: 10.1200/JCO.2009.25.0779. Epub 2009 Nov 2.
9
Early prediction of success or failure of treatment with second-generation tyrosine kinase inhibitors in patients with chronic myeloid leukemia.慢性髓性白血病患者第二代酪氨酸激酶抑制剂治疗成功或失败的早期预测。
Haematologica. 2010 Feb;95(2):224-31. doi: 10.3324/haematol.2009.012781. Epub 2009 Oct 14.
10
Finding of kinase domain mutations in patients with chronic phase chronic myeloid leukemia responding to imatinib may identify those at high risk of disease progression.在对伊马替尼有反应的慢性期慢性髓性白血病患者中发现激酶结构域突变,可能会识别出疾病进展风险高的患者。
J Clin Oncol. 2008 Oct 10;26(29):4806-13. doi: 10.1200/JCO.2008.16.9953. Epub 2008 Jul 21.

二线酪氨酸激酶抑制剂的应答持久:慢性髓性白血病患者的意向治疗分析。

Responses to second-line tyrosine kinase inhibitors are durable: an intention-to-treat analysis in chronic myeloid leukemia patients.

机构信息

Department of Haematology, Imperial College London, Hammersmith Hospital, London, United Kingdom.

出版信息

Blood. 2012 Feb 23;119(8):1838-43. doi: 10.1182/blood-2011-10-383000. Epub 2011 Dec 14.

DOI:10.1182/blood-2011-10-383000
PMID:22174159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5162552/
Abstract

Second-generation tyrosine kinase inhibitors (2G-TKIs) are effective at inducing complete cytogenetic responses (CCyRs) in approximately half of chronic myeloid leukemia patients treated while still in the chronic phase and after failing imatinib. It is less clear whether these responses are durable. In the present study, we report the clinical outcome of 119 patients who received a 2G-TKI as second-line treatment while still in the chronic phase. In an intention-to-treat analysis, the 4-year probabilities of overall and event-free survival were 81.9% and 35.3%, respectively. Sixty-two patients discontinued the initial 2G-TKI because of resistance or intolerance. To further explore the durability of cytogenetic responses, irrespective of the need for a third-line TKI, we used the concept of "current CCyR-survival" (c-CCyRS). The c-CCyRS at 4 years was 54.4%. After introduction of a 2G-TKI, 77 patients had a 3-month BCR-ABL1/ABL1 transcript ratio of ≤ 10% and had significantly superior overall survival (91.3% vs 72.1%, P = .02), event-free survival (49.3% vs 13.0%, P < .001), and c-CCyRS (67.2% vs 11.2%, P = .0001) compared with the 33 patients with ratios > 10%. The 3-month molecular response was the only independent predictor for overall survival. Using an intention-to-treat analysis, we have shown that the responses to second-line therapies are durable. Patients destined to fare poorly can be identified early during therapy.

摘要

第二代酪氨酸激酶抑制剂 (2G-TKIs) 在慢性髓性白血病患者慢性期和伊马替尼治疗失败后,能有效诱导约半数患者出现完全细胞遗传学反应 (CCyR)。但这些反应的持久性尚不清楚。本研究报告了 119 例患者在慢性期接受 2G-TKI 二线治疗的临床结果。意向治疗分析中,总生存和无事件生存的 4 年概率分别为 81.9%和 35.3%。62 例患者因耐药或不耐受而停止初始 2G-TKI。为了进一步探讨细胞遗传学反应的持久性,我们不顾及是否需要三线 TKI,使用了“当前 CCyR 生存”(c-CCyRS)的概念。4 年时的 c-CCyRS 为 54.4%。在引入 2G-TKI 后,77 例患者的 BCR-ABL1/ABL1 转录比值在 3 个月时≤10%,总生存显著改善(91.3% vs. 72.1%,P =.02)、无事件生存(49.3% vs. 13.0%,P <.001)和 c-CCyRS(67.2% vs. 11.2%,P =.0001)均优于比值>10%的 33 例患者。3 个月时的分子反应是总生存的唯一独立预测因素。采用意向治疗分析,我们发现二线治疗的反应是持久的。在治疗早期就能识别出预后不良的患者。