• 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

捷克共和国和斯洛伐克慢性髓性白血病患者接受酪氨酸激酶抑制剂治疗后的第二恶性肿瘤发生率。

Incidence of second malignancies during treatment of chronic myeloid leukemia with tyrosine kinase inhibitors in the Czech Republic and Slovakia.

机构信息

2nd Department of Internal Medicine, Division of Hematolgy, University Hospital Hradec Králové, Czech Republic.

出版信息

Neoplasma. 2011;58(3):256-62. doi: 10.4149/neo_2011_03_256.

DOI:10.4149/neo_2011_03_256
PMID:21395367
Abstract

Tyrosine kinase inhibitors (TKI) have completely changed the prognosis of patients with Ph+ chronic myeloid leukemia (CML). The occurrence of a second malignancy (SM) in CML patients successfully treated with TKI may significantly affect their prognosis. In a retrospective study of 1,038 patients with CML treated at 10 centers in the Czech Republic and Slovakia between 2000 and 2009, SM was detected in 35 (3.37%) patients after TKI therapy was initiated. The median intervals from the diagnosis of CML and from the start of TKI therapy to the diagnosis of SM were 58 months (range 2 - 214) and 32 months (range 1 - 102), respectively. The observed age-standardized incidence of SM after the start of TKI therapy was 8.95 / 1,000 person-years. Comparison of the incidence of SM in CML patients with population data was performed only for patients from the Czech Republic. The age-standardized incidence rate of all malignant tumors except non-melanoma skin cancers was 6.76 (95% CI: 6.74; 6.78) / 1,000 person-years in 2000 - 2007 while the incidence rate of SM in 708 CML patients from the Czech Republic treated with TKI was 9.84 (95% CI: 6.20; 13.48) / 1,000 person-years, i.e. 1.5-fold higher, although the difference was statistically insignificant. The distribution of SM types in CML patients treated with TKI was similar to that in the age-standardized general Czech population. The median overall survival (OS) of patients treated with TKI who also developed SM (57 months) was shorter than the OS of patients treated with TKI but not suffering from SM (median OS not reached, log rank test p < 0.001. Prospective long-term population-based studies in CML patients treated with TKI as first-line therapy are needed to determine the relationship of SM to KTI therapy.

摘要

酪氨酸激酶抑制剂 (TKI) 彻底改变了 Ph+ 慢性髓性白血病 (CML) 患者的预后。在成功接受 TKI 治疗的 CML 患者中,第二种恶性肿瘤 (SM) 的发生可能会显著影响其预后。在捷克共和国和斯洛伐克 10 个中心对 2000 年至 2009 年期间接受治疗的 1038 例 CML 患者进行的回顾性研究中,在开始 TKI 治疗后,有 35 例 (3.37%) 患者检测到 SM。从 CML 诊断到开始 TKI 治疗再到 SM 诊断的中位间隔分别为 58 个月(范围 2-214)和 32 个月(范围 1-102)。开始 TKI 治疗后 SM 的观察到的年龄标准化发病率为 8.95/1000 人年。仅对来自捷克共和国的 CML 患者进行了 SM 发病率与人群数据的比较。除非黑素瘤皮肤癌外,2000-2007 年所有恶性肿瘤的年龄标准化发病率为 6.76(95%CI:6.74;6.78)/1000 人年,而在捷克共和国接受 TKI 治疗的 708 例 CML 患者中,SM 的发病率为 9.84(95%CI:6.20;13.48)/1000 人年,即发病率增加了 1.5 倍,尽管差异无统计学意义。接受 TKI 治疗的 CML 患者中 SM 类型的分布与年龄标准化的捷克普通人群相似。同时患有 SM 的接受 TKI 治疗的患者的中位总生存期(OS)(57 个月)短于未患有 SM 的接受 TKI 治疗的患者的 OS(中位 OS 未达到,对数秩检验 p<0.001)。需要对接受 TKI 作为一线治疗的 CML 患者进行前瞻性长期基于人群的研究,以确定 SM 与 TKI 治疗的关系。

相似文献

1
Incidence of second malignancies during treatment of chronic myeloid leukemia with tyrosine kinase inhibitors in the Czech Republic and Slovakia.捷克共和国和斯洛伐克慢性髓性白血病患者接受酪氨酸激酶抑制剂治疗后的第二恶性肿瘤发生率。
Neoplasma. 2011;58(3):256-62. doi: 10.4149/neo_2011_03_256.
2
Incidence and outcome of second malignancies in patients with chronic myeloid leukemia during treatment with tyrosine kinase inhibitors.酪氨酸激酶抑制剂治疗慢性髓性白血病患者的二次恶性肿瘤的发生率和结局。
Med Oncol. 2018 May 30;35(7):99. doi: 10.1007/s12032-018-1159-7.
3
Incidence of Second Malignancies of Chronic Myeloid Leukemia During Treatment With Tyrosine Kinase Inhibitors.酪氨酸激酶抑制剂治疗慢性髓性白血病期间第二原发性恶性肿瘤的发生率
Clin Lymphoma Myeloma Leuk. 2016 Oct;16(10):577-581. doi: 10.1016/j.clml.2016.06.010. Epub 2016 Jun 8.
4
Prognostic factors and survival outcomes in patients with chronic myeloid leukemia in blast phase in the tyrosine kinase inhibitor era: Cohort study of 477 patients.酪氨酸激酶抑制剂时代慢性髓性白血病急变期患者的预后因素及生存结果:477例患者的队列研究
Cancer. 2017 Nov 15;123(22):4391-4402. doi: 10.1002/cncr.30864. Epub 2017 Jul 25.
5
Second malignancies following treatment of chronic myeloid leukaemia in the tyrosine kinase inhibitor era.酪氨酸激酶抑制剂时代慢性髓性白血病治疗后的第二恶性肿瘤。
Br J Haematol. 2015 Jun;169(5):683-8. doi: 10.1111/bjh.13346. Epub 2015 Mar 27.
6
BCR-ABL kinase domain mutations in tyrosine kinase inhibitors-naïve and -exposed Southeast Asian chronic myeloid leukemia patients.未接受过酪氨酸激酶抑制剂治疗和已暴露于酪氨酸激酶抑制剂的东南亚慢性髓性白血病患者的 BCR-ABL 激酶结构域突变。
Exp Mol Pathol. 2012 Apr;92(2):259-65. doi: 10.1016/j.yexmp.2012.01.007. Epub 2012 Jan 31.
7
Use patterns of first-line inhibitors of tyrosine kinase and time to change to second-line therapy in chronic myeloid leukemia.慢性髓性白血病中一线酪氨酸激酶抑制剂的使用模式及转换至二线治疗的时间
Int J Clin Pharm. 2017 Aug;39(4):851-859. doi: 10.1007/s11096-017-0484-9. Epub 2017 May 15.
8
Molecular monitoring of tyrosine kinase inhibitor therapy of chronic myeloid leukemia in China.中国慢性髓性白血病酪氨酸激酶抑制剂治疗的分子监测
J Cancer Res Clin Oncol. 2016 Jul;142(7):1549-55. doi: 10.1007/s00432-016-2158-8. Epub 2016 Apr 16.
9
Variables associated with patient-reported outcomes in persons with chronic myeloid leukemia receiving tyrosine kinase-inhibitor therapy.接受酪氨酸激酶抑制剂治疗的慢性髓性白血病患者中与患者报告结局相关的变量。
J Cancer Res Clin Oncol. 2017 Jun;143(6):1013-1022. doi: 10.1007/s00432-017-2353-2. Epub 2017 Mar 1.
10
Secondary malignancies in chronic myeloid leukemia patients after imatinib-based treatment: long-term observation in CML Study IV.伊马替尼治疗的慢性髓性白血病患者的继发性恶性肿瘤:CML研究IV的长期观察
Leukemia. 2016 Jun;30(6):1255-62. doi: 10.1038/leu.2016.20. Epub 2016 Feb 9.

引用本文的文献

1
Clinical features and prognosis of duplex primary malignant neoplasms involving chronic myeloid leukemia.涉及慢性粒细胞白血病的双原发性恶性肿瘤的临床特征与预后
Medicine (Baltimore). 2020 Oct 30;99(44):e22904. doi: 10.1097/MD.0000000000022904.
2
Incidence and outcome of second malignancies in patients with chronic myeloid leukemia during treatment with tyrosine kinase inhibitors.酪氨酸激酶抑制剂治疗慢性髓性白血病患者的二次恶性肿瘤的发生率和结局。
Med Oncol. 2018 May 30;35(7):99. doi: 10.1007/s12032-018-1159-7.
3
An observational study on risk of secondary cancers in chronic myeloid leukemia patients in the TKI era in the United States.
美国TKI时代慢性髓性白血病患者继发癌症风险的观察性研究。
PeerJ. 2018 Feb 12;6:e4342. doi: 10.7717/peerj.4342. eCollection 2018.
4
Nilotinib Induced Recurrent Gastric Polyps: Case Report and Review of Literature.尼洛替尼诱发复发性胃息肉:病例报告及文献综述
Am J Case Rep. 2017 Jul 14;18:794-798. doi: 10.12659/ajcr.903485.
5
Incidence of second primary malignancies and related mortality in patients with imatinib-treated chronic myeloid leukemia.伊马替尼治疗慢性髓性白血病患者的第二原发性恶性肿瘤的发生率和相关死亡率。
Haematologica. 2017 Sep;102(9):1530-1536. doi: 10.3324/haematol.2017.169532. Epub 2017 Jun 1.
6
CML as Part of Dual Malignancies-A Retrospective Analysis: Possible Mechanisms and Review of Literature.慢性粒细胞白血病作为双恶性肿瘤的一部分——一项回顾性分析:可能机制及文献综述
Indian J Hematol Blood Transfus. 2016 Dec;32(4):392-396. doi: 10.1007/s12288-015-0621-3. Epub 2015 Nov 21.
7
Secondary malignancies in chronic myeloid leukemia patients after imatinib-based treatment: long-term observation in CML Study IV.伊马替尼治疗的慢性髓性白血病患者的继发性恶性肿瘤:CML研究IV的长期观察
Leukemia. 2016 Jun;30(6):1255-62. doi: 10.1038/leu.2016.20. Epub 2016 Feb 9.
8
Molecular investigation of coexistent chronic myeloid leukaemia and peripheral T-cell lymphoma - a case report.慢性髓性白血病与外周T细胞淋巴瘤共存的分子研究——病例报告
Sci Rep. 2015 Oct 6;5:14829. doi: 10.1038/srep14829.
9
Occurrence of Carcinoma of the Pancreas Following Nilotinib Therapy for Chronic Myeloid Leukemia: Report of a Case with Review of the Literature.尼洛替尼治疗慢性髓性白血病后发生胰腺癌:1例报告并文献复习
Turk J Haematol. 2015 Sep;32(3):257-62. doi: 10.4274/tjh.2013.0322.
10
Occurrence of secondary malignancies in chronic myeloid leukemia during therapy with imatinib mesylate-single institution experience.甲磺酸伊马替尼治疗慢性髓性白血病期间继发恶性肿瘤的发生情况——单机构经验
Mediterr J Hematol Infect Dis. 2015 Jan 1;7(1):e2015003. doi: 10.4084/MJHID.2015.003. eCollection 2015.