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本文引用的文献

1
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.
2
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.
3
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。
Blood. 2009 Sep 3;114(10):2037-43. doi: 10.1182/blood-2009-01-197715. Epub 2009 Jun 30.
4
Activity of bosutinib, dasatinib, and nilotinib against 18 imatinib-resistant BCR/ABL mutants.博舒替尼、达沙替尼和尼罗替尼对18种伊马替尼耐药的BCR/ABL突变体的活性。
J Clin Oncol. 2009 Jan 20;27(3):469-71. doi: 10.1200/JCO.2008.19.8853. Epub 2008 Dec 15.
5
Failure to achieve a major cytogenetic response by 12 months defines inadequate response in patients receiving nilotinib or dasatinib as second or subsequent line therapy for chronic myeloid leukemia.接受尼洛替尼或达沙替尼作为慢性髓性白血病二线或后续治疗的患者,若在12个月时未达到主要细胞遗传学反应,则定义为反应不足。
Blood. 2008 Aug 1;112(3):516-8. doi: 10.1182/blood-2008-02-141580. Epub 2008 May 20.
6
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.
7
Bcr-Abl kinase domain mutations, drug resistance, and the road to a cure for chronic myeloid leukemia.Bcr-Abl激酶结构域突变、耐药性与慢性髓性白血病的治愈之路
Blood. 2007 Oct 1;110(7):2242-9. doi: 10.1182/blood-2007-03-066936. Epub 2007 May 11.
8
Current and emerging treatment options in chronic myeloid leukemia.慢性髓性白血病的现有及新出现的治疗选择
Cancer. 2007 Jun 1;109(11):2171-81. doi: 10.1002/cncr.22661.
9
Identification of BCR-ABL point mutations conferring resistance to the Abl kinase inhibitor AMN107 (nilotinib) by a random mutagenesis study.通过随机诱变研究鉴定赋予对Abl激酶抑制剂AMN107(尼洛替尼)耐药性的BCR-ABL点突变
Blood. 2007 Jun 1;109(11):5011-5. doi: 10.1182/blood-2006-01-015347. Epub 2007 Feb 15.
10
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.

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。

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.

机构信息

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

出版信息

Blood. 2011 Feb 10;117(6):1822-7. doi: 10.1182/blood-2010-07-293977. Epub 2010 Oct 28.

DOI:10.1182/blood-2010-07-293977
PMID:21030554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4081281/
Abstract

We assessed the predictive factors for outcome and response in 123 patients with chronic myeloid leukemia in chronic phase treated with second-generation tyrosine kinase inhibitors (TKIs) after imatinib failure. Better event-free survival rates with second-generation TKI therapy were associated with a previous cytogenetic response to imatinib (P < .001) and a performance status of 0 (P = .001). Patients with 0, 1, or 2 adverse factors had 2-year event-free survival rates of 78%, 49%, and 20% (P < .001), respectively; 2-year overall survival rates of 95%, 85%, and 40%, (P = .002), respectively; and a 12-month probability of achieving a major cytogenetic response of 64%, 36%, and 20% (P = .007), respectively. In conclusion, patients with poor performance status and no previous cytogenetic response to imatinib therapy have a low likelihood of responding to second-generation TKI with poor event-free survival and therefore should be offered additional treatment options. This scoring system could serve to advise patients of their prognosis and treatment options, as well as to evaluate the benefit of newer alternate options.

摘要

我们评估了 123 例慢性髓性白血病慢性期患者在伊马替尼治疗失败后接受第二代酪氨酸激酶抑制剂(TKI)治疗的结局和反应的预测因素。第二代 TKI 治疗具有更好的无事件生存(EFS)率,与伊马替尼的先前细胞遗传学反应(P <.001)和表现状态为 0(P =.001)有关。无不良因素、有 1 个或 2 个不良因素的患者,2 年 EFS 率分别为 78%、49%和 20%(P <.001);2 年总生存率分别为 95%、85%和 40%(P =.002);12 个月时获得主要细胞遗传学反应的概率分别为 64%、36%和 20%(P =.007)。总之,表现状态差且对伊马替尼治疗无先前细胞遗传学反应的患者对第二代 TKI 反应的可能性较低,EFS 不良,因此应提供其他治疗选择。该评分系统可用于告知患者预后和治疗选择,并评估新的替代方案的获益。