• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

选择哪种酪氨酸激酶抑制剂?慢性髓性白血病患者面临众多选择的困境。

Which TKI? An embarrassment of riches for chronic myeloid leukemia patients.

作者信息

Hughes Timothy, White Deborah

机构信息

1South Australian Health and Medical Research Institute, SA Pathology, and University of Adelaide, Adelaide, Australia.

出版信息

Hematology Am Soc Hematol Educ Program. 2013;2013:168-75. doi: 10.1182/asheducation-2013.1.168.

DOI:10.1182/asheducation-2013.1.168
PMID:24319178
Abstract

With the approval in many countries of nilotinib and dasatinib for frontline therapy in chronic myeloid leukemia, clinicians now have to make a difficult choice. Because none of the 3 available tyrosine kinase inhibitors (TKIs) have shown a clear survival advantage, they all represent reasonable choices. However, in individual patients, the case may be stronger for a particular TKI. In the younger patient, in whom the prospect of eventually achieving treatment-free remission is likely to be of great importance, dasatinib or nilotinib may be preferred, although their advantage over imatinib in this setting remains to be proven. In patients with a higher risk of transformation (which is currently based on prognostic scoring), the more potent TKIs may be preferred because they appear to be more effective at reducing the risk of transformation to BC. However, imatinib still represents an excellent choice for many chronic myeloid leukemia patients. All of these considerations need to be made in the context of the patient's comorbidities, which may lead to one or more TKIs being ruled out of contention. Whatever first choice of TKI is made, treatment failure or intolerance must be recognized early because a prompt switch to another TKI likely provides the best chance of achieving optimal response.

摘要

随着尼洛替尼和达沙替尼在许多国家被批准用于慢性髓性白血病的一线治疗,临床医生现在不得不做出艰难的选择。由于现有的3种酪氨酸激酶抑制剂(TKIs)均未显示出明显的生存优势,它们都代表了合理的选择。然而,对于个别患者而言,可能更倾向于选择某一种特定的TKI。对于年轻患者,最终实现无治疗缓解的前景可能非常重要,达沙替尼或尼洛替尼可能更受青睐,尽管它们在此情况下相对于伊马替尼的优势仍有待证实。对于具有较高转化风险的患者(目前基于预后评分),可能更倾向于选择效力更强的TKIs,因为它们似乎在降低转化为急变期(BC)的风险方面更有效。然而,伊马替尼对于许多慢性髓性白血病患者而言仍是一个绝佳的选择。所有这些考虑都需要结合患者的合并症来进行,合并症可能导致一种或多种TKIs被排除在选择范围之外。无论首次选择何种TKI,都必须尽早识别治疗失败或不耐受情况,因为及时换用另一种TKI可能为实现最佳反应提供最佳机会。

相似文献

1
Which TKI? An embarrassment of riches for chronic myeloid leukemia patients.选择哪种酪氨酸激酶抑制剂?慢性髓性白血病患者面临众多选择的困境。
Hematology Am Soc Hematol Educ Program. 2013;2013:168-75. doi: 10.1182/asheducation-2013.1.168.
2
Treatment-, patient-, and disease-related factors and the emergence of adverse events with tyrosine kinase inhibitors for the treatment of chronic myeloid leukemia.治疗相关因素、患者相关因素和疾病相关因素与酪氨酸激酶抑制剂治疗慢性髓系白血病的不良反应的发生有关。
Pharmacotherapy. 2013 Aug;33(8):868-81. doi: 10.1002/phar.1266. Epub 2013 Apr 3.
3
Chemical proteomic profiles of the BCR-ABL inhibitors imatinib, nilotinib, and dasatinib reveal novel kinase and nonkinase targets.BCR-ABL抑制剂伊马替尼、尼洛替尼和达沙替尼的化学蛋白质组学图谱揭示了新的激酶和非激酶靶点。
Blood. 2007 Dec 1;110(12):4055-63. doi: 10.1182/blood-2007-07-102061. Epub 2007 Aug 24.
4
Selecting the best frontline treatment in chronic myeloid leukemia.选择慢性髓性白血病的最佳一线治疗方案。
Curr Hematol Malig Rep. 2015 Jun;10(2):145-57. doi: 10.1007/s11899-015-0254-5.
5
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.
6
BCR-ABL tyrosine kinase inhibitors in chronic myeloid leukemia: using guidelines to make rational treatment choices.慢性髓性白血病中的BCR-ABL酪氨酸激酶抑制剂:依据指南做出合理的治疗选择
J Natl Compr Canc Netw. 2008 Mar;6 Suppl 2:S37-42; quiz S43-S44.
7
Frequency of ABL gene mutations in chronic myeloid leukemia patients resistant to imatinib and results of treatment switch to second-generation tyrosine kinase inhibitors.伊马替尼耐药的慢性髓性白血病患者的 ABL 基因突变频率及治疗转换为第二代酪氨酸激酶抑制剂的结果。
Med Clin (Barc). 2013 Aug 4;141(3):95-9. doi: 10.1016/j.medcli.2012.10.028. Epub 2013 Feb 22.
8
Real-world analysis of tyrosine kinase inhibitor treatment patterns among patients with chronic myeloid leukemia in the United States.美国慢性髓性白血病患者酪氨酸激酶抑制剂治疗模式的真实世界分析。
Clin Ther. 2015 Jan 1;37(1):124-33. doi: 10.1016/j.clinthera.2014.10.019. Epub 2014 Nov 22.
9
Improving frontline treatment for chronic myeloid leukemia: emerging evidence for use of nilotinib and dasatinib.改善慢性髓性白血病的一线治疗:尼洛替尼和达沙替尼应用的新证据
Clin Adv Hematol Oncol. 2011 Oct;9(10):734-45.
10
Cost-effectiveness of nilotinib, dasatinib and imatinib as first-line treatment for chronic myeloid leukemia in Colombia, 2012.2012年,尼洛替尼、达沙替尼和伊马替尼作为哥伦比亚慢性髓性白血病一线治疗药物的成本效益分析
Biomedica. 2014 Jan-Mar;34(1):48-59. doi: 10.1590/S0120-41572014000100008.

引用本文的文献

1
miR-15a targets the HSP90 co-chaperone Morgana in chronic myeloid leukemia.miR-15a 靶向慢性髓性白血病中的 HSP90 共伴侣 Morgana。
Sci Rep. 2024 Jul 2;14(1):15089. doi: 10.1038/s41598-024-65404-7.
2
Adverse outcomes for chronic myeloid leukemia patients with splenomegaly and low in vivo kinase inhibition on imatinib.伴有巨脾和伊马替尼体内激酶抑制率低的慢性髓性白血病患者的不良结局。
Blood Cancer J. 2023 Sep 11;13(1):143. doi: 10.1038/s41408-023-00917-4.
3
Cross-Domain Text Mining to Predict Adverse Events from Tyrosine Kinase Inhibitors for Chronic Myeloid Leukemia.
跨领域文本挖掘以预测慢性髓性白血病酪氨酸激酶抑制剂的不良事件
Cancers (Basel). 2022 Sep 26;14(19):4686. doi: 10.3390/cancers14194686.
4
Alterations in cellular metabolisms after Imatinib therapy: a review.伊马替尼治疗后的细胞代谢改变:综述。
Med Oncol. 2022 May 16;39(5):95. doi: 10.1007/s12032-022-01699-8.
5
Meta-Analysis of Gastrointestinal Adverse Events from Tyrosine Kinase Inhibitors for Chronic Myeloid Leukemia.酪氨酸激酶抑制剂治疗慢性髓性白血病所致胃肠道不良事件的Meta分析
Cancers (Basel). 2021 Apr 1;13(7):1643. doi: 10.3390/cancers13071643.
6
Managing chronic myeloid leukemia for treatment-free remission: a proposal from the GIMEMA CML WP.管理无治疗缓解的慢性髓性白血病:来自 GIMEMA CML WP 的建议。
Blood Adv. 2019 Dec 23;3(24):4280-4290. doi: 10.1182/bloodadvances.2019000865.
7
Gene expression signature that predicts early molecular response failure in chronic-phase CML patients on frontline imatinib.能预测一线伊马替尼治疗慢性期 CML 患者早期分子反应失败的基因表达特征。
Blood Adv. 2019 May 28;3(10):1610-1621. doi: 10.1182/bloodadvances.2019000195.
8
Primary imatinib failure rescued by dasatinib and maintained by reintroduction of imatinib.原发性伊马替尼耐药经达沙替尼挽救后,通过重新引入伊马替尼得以维持。
Rev Bras Hematol Hemoter. 2017 Oct-Dec;39(4):360-363. doi: 10.1016/j.bjhh.2017.06.006. Epub 2017 Jul 26.
9
Characterization of Patients with Chronic Myeloid Leukemia Unresponsive to Tyrosine Kinase Inhibitors Who Underwent Allogeneic Hematopoietic Stem Cell Transplantation.对接受异基因造血干细胞移植但对酪氨酸激酶抑制剂无反应的慢性髓性白血病患者的特征分析。
Int J Hematol Oncol Stem Cell Res. 2017 Jan 1;11(1):30-36.
10
Increased peroxisome proliferator-activated receptor γ activity reduces imatinib uptake and efficacy in chronic myeloid leukemia mononuclear cells.过氧化物酶体增殖物激活受体γ活性增加会降低伊马替尼在慢性髓性白血病单核细胞中的摄取及疗效。
Haematologica. 2017 May;102(5):843-853. doi: 10.3324/haematol.2016.153270. Epub 2017 Feb 2.