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2
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本文引用的文献

1
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.
2
The use of nilotinib or dasatinib after failure to 2 prior tyrosine kinase inhibitors: long-term follow-up.在两种先前的酪氨酸激酶抑制剂治疗失败后使用尼罗替尼或达沙替尼:长期随访
Blood. 2009 Nov 12;114(20):4361-8. doi: 10.1182/blood-2009-05-221531. Epub 2009 Sep 3.
3
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.
4
Imatinib for newly diagnosed patients with chronic myeloid leukemia: incidence of sustained responses in an intention-to-treat analysis.伊马替尼用于新诊断的慢性髓性白血病患者:意向性治疗分析中的持续缓解发生率
J Clin Oncol. 2008 Jul 10;26(20):3358-63. doi: 10.1200/JCO.2007.15.8154. Epub 2008 Jun 2.
5
Dasatinib induces durable cytogenetic responses in patients with chronic myelogenous leukemia in chronic phase with resistance or intolerance to imatinib.达沙替尼可使对伊马替尼耐药或不耐受的慢性期慢性髓性白血病患者产生持久的细胞遗传学反应。
Leukemia. 2008 Jun;22(6):1200-6. doi: 10.1038/leu.2008.84. Epub 2008 Apr 10.
6
Part II: management of resistance to imatinib in chronic myeloid leukaemia.第二部分:慢性髓性白血病中对伊马替尼耐药的管理。
Lancet Oncol. 2007 Dec;8(12):1116-1128. doi: 10.1016/S1470-2045(07)70379-0.
7
Nilotinib (formerly AMN107), a highly selective BCR-ABL tyrosine kinase inhibitor, is effective in patients with Philadelphia chromosome-positive chronic myelogenous leukemia in chronic phase following imatinib resistance and intolerance.尼罗替尼(原AMN107)是一种高度选择性的BCR-ABL酪氨酸激酶抑制剂,对伊马替尼耐药和不耐受的慢性期费城染色体阳性慢性髓性白血病患者有效。
Blood. 2007 Nov 15;110(10):3540-6. doi: 10.1182/blood-2007-03-080689. Epub 2007 Aug 22.
8
Dasatinib induces notable hematologic and cytogenetic responses in chronic-phase chronic myeloid leukemia after failure of imatinib therapy.达沙替尼在伊马替尼治疗失败后的慢性期慢性髓性白血病中可诱导显著的血液学和细胞遗传学反应。
Blood. 2007 Mar 15;109(6):2303-9. doi: 10.1182/blood-2006-09-047266. Epub 2006 Nov 30.
9
Nilotinib in imatinib-resistant CML and Philadelphia chromosome-positive ALL.尼洛替尼用于伊马替尼耐药的慢性粒细胞白血病和费城染色体阳性的急性淋巴细胞白血病。
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10
Dasatinib in imatinib-resistant Philadelphia chromosome-positive leukemias.达沙替尼用于伊马替尼耐药的费城染色体阳性白血病。
N Engl J Med. 2006 Jun 15;354(24):2531-41. doi: 10.1056/NEJMoa055229.

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。

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.

机构信息

Department of Haematology, Imperial College London, London, UK.

出版信息

Blood. 2010 Dec 16;116(25):5497-500. doi: 10.1182/blood-2010-06-291922. Epub 2010 Sep 10.

DOI:10.1182/blood-2010-06-291922
PMID:20833982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6143154/
Abstract

We analyzed a cohort of 26 patients with chronic myeloid leukemia who had failed imatinib and a second tyrosine kinase inhibitor but were still in first chronic phase and identified prognostic factors for response and outcomes. The achievement of a prior cytogenetic response on imatinib or on second-line therapy were the only independent predictors for the achievement of complete cytogenetic responses on third-line therapy. Younger age and the achievement of a cytogenetic response on second line were the only independent predictors for overall survival (OS). At 3 months, the 9 patients who had achieved a cytogenetic response had better 30-month probabilities of complete cytogenetic responses and OS than the patients who had failed to do so. Factors measurable before starting treatment with third line therapy and cytogenetic responses at 3 months can accurately predict subsequent outcome and thus guide clinical decisions.

摘要

我们分析了 26 例慢性髓性白血病患者的队列,这些患者在使用伊马替尼和第二种酪氨酸激酶抑制剂后失败,但仍处于慢性期 1 期,并确定了对第三线治疗反应和结局的预后因素。在伊马替尼或二线治疗中取得的先前细胞遗传学反应是在三线治疗中获得完全细胞遗传学反应的唯一独立预测因素。较年轻的年龄和二线治疗中取得的细胞遗传学反应是总生存(OS)的唯一独立预测因素。在 3 个月时,获得细胞遗传学反应的 9 例患者在 30 个月时具有更高的完全细胞遗传学反应和 OS 概率,而未获得反应的患者则不然。在开始三线治疗前可测量的因素和 3 个月时的细胞遗传学反应可以准确预测后续结果,从而指导临床决策。