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Predicting complete cytogenetic response and subsequent progression-free survival in 2060 patients with CML on imatinib treatment: the EUTOS score.在伊马替尼治疗的 2060 例 CML 患者中预测完全细胞遗传学反应和随后的无进展生存:EUTOS 评分。
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Research challenges in adolescent and young adult cancer survivor research.青少年和青年癌症幸存者研究中的研究挑战。
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Treatment of pediatric chronic myeloid leukemia in the year 2010: use of tyrosine kinase inhibitors and stem-cell transplantation.2010 年儿童慢性髓性白血病的治疗:酪氨酸激酶抑制剂和干细胞移植的应用。
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Nilotinib is effective in patients with chronic myeloid leukemia in chronic phase after imatinib resistance or intolerance: 24-month follow-up results.尼洛替尼治疗伊马替尼耐药或不耐受的慢性期慢性髓性白血病患者有效:24 个月随访结果。
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"Real-life" results of front-line treatment with Imatinib in older patients (≥ 65 years) with newly diagnosed chronic myelogenous leukemia.新诊断的慢性髓性白血病老年患者(≥65 岁)一线伊马替尼治疗的“真实世界”结果。
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酪氨酸激酶抑制剂 upfront 治疗的青少年及青年慢性髓性白血病患者结局分析。

Analysis of outcomes in adolescents and young adults with chronic myelogenous leukemia treated with upfront tyrosine kinase inhibitor therapy.

机构信息

Department of Leukemia, University of Texas, Anderson Cancer Center, Houston, TX 77230, USA.

出版信息

Haematologica. 2012 Jul;97(7):1029-35. doi: 10.3324/haematol.2011.056721. Epub 2012 Jan 22.

DOI:10.3324/haematol.2011.056721
PMID:22271898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3396674/
Abstract

BACKGROUND

Outcomes in chronic myeloid leukemia have improved with tyrosine kinase inhibitor treatment. However, little is known about outcomes of chronic myeloid leukemia in adolescent and young adult patients.

DESIGN AND METHODS

We reviewed all 468 chronic myeloid leukemia patients treated at our institution with tyrosine kinase inhibitors as initial therapy: imatinib (n=281), nilotinib (n=98) or dasatinib (n=89).

RESULTS

Median age was 47 years, median follow up 71 months and median treatment time with initial tyrosine kinase inhibitors 48 months. Adolescent and young adult was defined as aged 15-29 years. Sixty-one adolescent and young adult patients were identified. The only significant differences between adolescent and young adult and older patients were incidence of splenomegaly and distribution in Sokal risk groups. Only 3 adolescent and young adult patients have died. Rates of complete cytogenetic, major molecular and complete molecular response were significantly higher in older patients compared to adolescent and young adult patients, with a favorable trend in event-free survival for older patients. Transformation-free and overall survival were similar for the two groups.

CONCLUSIONS

The unfavorable trend in outcome for adolescent and young adult patients with chronic myeloid leukemia is unexpected. Additional research in this population is required to better define outcomes, understand the cause of this difference, and to help make better treatment recommendations.

摘要

背景

慢性髓性白血病患者的治疗效果随着酪氨酸激酶抑制剂的治疗而得到改善。然而,对于青少年和年轻成年患者的慢性髓性白血病的治疗效果,我们知之甚少。

设计与方法

我们回顾了在我们机构接受酪氨酸激酶抑制剂作为初始治疗的 468 例慢性髓性白血病患者的所有数据:伊马替尼(n=281)、尼洛替尼(n=98)或达沙替尼(n=89)。

结果

中位年龄为 47 岁,中位随访时间为 71 个月,初始酪氨酸激酶抑制剂治疗时间的中位数为 48 个月。将年龄在 15-29 岁的患者定义为青少年和年轻成年患者。共确定了 61 例青少年和年轻成年患者。青少年和年轻成年患者与老年患者之间仅存在显著差异,包括脾肿大的发生率和 Sokal 风险组的分布。仅有 3 例青少年和年轻成年患者死亡。与青少年和年轻成年患者相比,老年患者的完全细胞遗传学缓解、主要分子缓解和完全分子缓解的比例明显更高,且老年患者的无事件生存呈有利趋势。两组的无转化生存和总生存相似。

结论

青少年和年轻成年慢性髓性白血病患者的治疗效果出现不利趋势,这是出乎意料的。需要对该人群进行更多的研究,以更好地定义结局,了解这种差异的原因,并为制定更好的治疗建议提供帮助。