Suppr超能文献

自伊马替尼治疗问世以来美国费城染色体阳性慢性髓性白血病的结局:监测、流行病学和最终结果数据库,2000-2019 年。

Outcome of Philadelphia chromosome-positive chronic myeloid leukemia in the United States since the introduction of imatinib therapy-The Surveillance, Epidemiology, and End Results database, 2000-2019.

机构信息

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

出版信息

Cancer. 2023 Dec 1;129(23):3805-3814. doi: 10.1002/cncr.35038. Epub 2023 Sep 28.

Abstract

BACKGROUND

Since the introduction of BCR::ABL1 tyrosine kinase inhibitors (TKIs) in 2000, the treatment of Philadelphia chromosome (Ph)-positive chronic myeloid leukemia (CML) has improved significantly.

METHODS

This study aimed to evaluate Ph-positive CML outcomes in the TKI therapy era, considering factors like age, ethnicity, and income. Using the Surveillance, Epidemiology, and End Results (SEER) database, 2857 patients with Ph-positive CML diagnosed from 2000 to 2019 were analyzed.

RESULTS

The overall 5-year survival rates in Ph-positive CML increased to above 80%, compared with pre-TKIs historical data reporting 5-year overall survival (OS) rates of less than 50%. The 5-year OS rate was 73% for patients diagnosed in 2000-2004, 82% in 2005-2009, and 78% in 2010-2014; the 4-year OS rate was 83% in 2015-2019. The 5-year OS rate for younger patients (<60 years old) was 88% in 2000-2009 and 90% in 2010-2019 (p value .426). In older patients (60+ years old), the 5-year OS rates were 64% and 65%, respectively (p value, .303). Lower household income was associated with inferior survival across the 2000-2019. These results are inferior to European studies where TKIs are universally available and affordable, and relative OS in CML is similar to age-matched normal populations.

CONCLUSIONS

Although the outcome of Ph-positive CML has improved significantly since 2000, the SEER data still shows differences in outcomes among patient subsets, some anticipated (worse OS in older patients accounted by the relative OS), but others that suggest less than universal access and affordability of this therapy (among poorer patients) in the United States.

摘要

背景

自 2000 年 BCR::ABL1 酪氨酸激酶抑制剂(TKI)问世以来,费城染色体(Ph)阳性慢性髓性白血病(CML)的治疗得到了显著改善。

方法

本研究旨在评估 TKI 治疗时代 Ph 阳性 CML 的结果,同时考虑年龄、种族和收入等因素。利用监测、流行病学和最终结果(SEER)数据库,分析了 2000 年至 2019 年间诊断为 Ph 阳性 CML 的 2857 例患者。

结果

与 TKI 治疗前的历史数据(5 年总生存率(OS)不足 50%)相比,Ph 阳性 CML 的总体 5 年生存率提高至 80%以上。2000-2004 年诊断的患者 5 年 OS 率为 73%,2005-2009 年为 82%,2010-2014 年为 78%;4 年 OS 率为 2015-2019 年的 83%。年轻患者(<60 岁)的 5 年 OS 率在 2000-2009 年为 88%,在 2010-2019 年为 90%(p 值.426)。在老年患者(60 岁以上)中,5 年 OS 率分别为 64%和 65%(p 值.303)。较低的家庭收入与 2000-2019 年期间的生存不良相关。这些结果逊于欧洲研究,在欧洲,TKI 普遍可用且负担得起,CML 的相对 OS 与年龄匹配的正常人群相似。

结论

尽管自 2000 年以来,Ph 阳性 CML 的治疗结果有了显著改善,但 SEER 数据仍显示出患者亚组之间结果存在差异,其中一些差异是预期的(老年患者的 OS 较差,与相对 OS 一致),而另一些差异则表明 TKI 的可及性和可负担性并不普遍(在美国的贫困患者中)。

相似文献

引用本文的文献

1
NK cell-based immunotherapy strategies for myeloid leukemia.基于自然杀伤细胞的髓系白血病免疫治疗策略
Front Immunol. 2025 Jul 14;16:1621885. doi: 10.3389/fimmu.2025.1621885. eCollection 2025.
6
Outcome of 3q26.2/MECOM rearrangements in chronic myeloid leukemia.3q26.2/MECOM 重排慢性髓性白血病的转归。
Int J Hematol. 2024 Aug;120(2):203-211. doi: 10.1007/s12185-024-03787-z. Epub 2024 May 15.

本文引用的文献

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