期刊文献+

伊马替尼治疗早期BCR-ABL转录本水平在251例慢性髓性白血病患者中的预后价值 被引量:7

The prognostic value of early BCR-ABL transcripts level in 251 patients with chronic myeloid leukemia after treatment with imatinib
原文传递
导出
摘要 目的 了解慢性髓性白血病(CML)患者伊马替尼治疗早期BCR-ABL转录本水平的预后价值,为CML患者早期预后评估和治疗选择提供依据.方法 回顾性分析251例接受伊马替尼—线治疗CML慢性期(CML-CP)患者的临床资料,分别比较治疗后3个月及6个月不同BCR-ABL转录本水平患者的无进展生存(PFS)率及总体生存(OS)率,并采用卡方检验及Logistic回归分析方法分析疾病进展的危险因素.结果 伊马替尼治疗3个月BCR-ABL转录本>10%组(92例)、>1%~10%组(94例)、≤1%组(65例)的PFS率分别为53.3%、71.3%、86.2% (P<0.05),OS率分别为92.4%、96.8%和93.8% (P>0.05).伊马替尼治疗后6个月时BCR-ABL转录本>10%组(22例)、>1%~10%(50例)组、≤1%(110例)组PFS率分别为27.3%、66.0%和82.7%(P<0.05),OS率分别为86.4%、94.0%、100%(P<0.05).Logistic回归分析结果显示3个月及6个月BCR-ABL转录本水平为影响疾病进展的独立危险因素.结论 伊马替尼治疗3个月及6个月BCR-ABL转录本水平对CML患者预后评估具有重要价值. Objective To understand the prognostic value of early monitoring BCR-ABL transcripts in patients with chronic myeloid leukemia(CML) after treatment with imatinib,and to provide the information for early assessment of prognosis and treatment options.Methods The clinical data of 251 patients with CML in chronic phase (CML-CP) who received imatinib as first-line therapy were retrospectively analyzed,the progression-free survival (PFS) and overall survival (OS) between different BCR-ABL transcriptional level at 3 and 6 month after imatinib treatment were compared.Meanwhile,Chi-square test and logistic regression were used to analyze the risk factors for disease progression.Results At 3 months after imatinib treatment BCR-ABL transcriptional levels〉10%,〉1%-≤10% and ≤1% were found in 92,94and 64patients,their PFS were 53.3%,71.3% and 86.2%,respectively.The results showed that the PFS of patients with low BCR-ABL transcriptional levels was significantly superior to that with high BCR-ABL transcriptional levels for CML at 3 months treatment (P〈0.05).The OS of three group did not reach statistical significance (92.4% vs 96.8% vs 93.8%,P〉0.05).When 182 patients receivedimatinib treatment at 6 months,22 patients with BCR-ABL transcriptional levels〉10%,50〉1%-≤10% and 110 ≤1%,their PFS were 27.3% vs 66.0% vs 82.7%(P〈0.05),the OS of three groups were 86.4% vs 94.0% vs 100%.There were significant differences among the three groups (P〈0.05).Logistic regression confirmed that the level of BCR-ABL transcriptional level at 3 and 6 months after imatinib treatment was independent factor to influence the progress of disease.Conclusion It is important for the prognosis evaluation of CML patients to monitor BCR-ABL transcriptional level at 3 and 6 months after imatinib treatment.
出处 《中华血液学杂志》 CAS CSCD 北大核心 2015年第7期553-558,共6页 Chinese Journal of Hematology
基金 国家高科技研究发展计划(863计划)(2012AA02A505) “江苏省临床医学中心”资质项目(ZX201102) 江苏高校优势学科建设工程资助项目(PAPD) 国家临床重点专科建设项目
关键词 白血病 髓系慢性 BCR-ABL阳性 伊马替尼 BCR-ABL转录本 预后 生存分析 Leukemia,myelogenous,chronic,BCR-ABL positive Imatinib BCR-ABL transcripts Prognosis Survival analysis
  • 相关文献

参考文献13

  • 1Goldman JM, Melo JV. Chronic myeloid leukemia-advances in biology and new approaches to treatment [J]. N Engl J Med, 2003, 349(15):1451-1464.
  • 2Druker B J, Guilhot F, O' Brien SG, et al. Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia [J]. N Engl J Med, 2006, 355(23):2408-2417.
  • 3Marin D, Hedgley C, Clark RE, et al. Predictive value of early molecular response in patients with chronic myeloid leukemia treated with first-line dasatinib [J]. Blood, 2012,120 (2):291- 294.
  • 4Hanfstein B, Muller MC, Hehlmann R, et al. Early molecular and cytogenetic response is predictive for long-term progression- free and overall survival in chronic myeloid leukemia (CML) [J]. Leukemia, 2012, 26(9):2096-2102.
  • 5Hughes TP, Hochhaus A, Branford S, et al. Long-term prognostic significance of early molecular response to imatinib in newly diagnosed chronic myeloid leukemia: an analysis from the International Randomized Study of Interferon and STI571 (IRIS) [J]. Blood, 2010, 116( 19):3758-3765.
  • 6中国慢性髓性白血病诊断与治疗指南(2013年版)[J].中华血液学杂志,2013,34(5):464-470. 被引量:92
  • 7秦亚溱,林振兴,岑建农,李小青,李庆华,程辉,耿素霞,王云贵,马道新,乔纯,李金兰,李玲娣,黄晓军.用于转换国际标准的BCR-ABL(P210)转录本水平的转换系数多中心确认研究[J].中华血液学杂志,2014,35(2):134-137. 被引量:13
  • 8Marin D, Ibrahim AR, Lucas C, et al. Assessment of BCR- ABL1 transcript levels at 3 months is the only requirement for predicting outcome for patients with chronic myeloid leukemia treated with tyrosine kinase inhibitors[J]. J Clin Oncol, 2012, 30 (3):232-238.
  • 9Matin D, Bazeos A, Mahon FX, et al. Adherence is the critical factor for achieving molecular responses in patients with chronic myeloid leukemia who achieve complete cytogenetic responses on imatinib[ J]. J Clin Oncol, 2010, 28( 14):2381-2388.
  • 10Jabbour E, Kantarjian HM, Saglio G, et al. Early response with dasatinib or imatinib in chronic myeloid leukemia: 3-year fol- low-up from a randomized phase 3 trial (DASISION) [J]. Blood, 2014, 123(4):494-500.

二级参考文献70

  • 1黄河,蔡真,林茂芳,谢万灼,梁彬,李黎,何静松,罗依,郑伟燕,张洁,叶琇锦,胡晓蓉,陈水云,金爱云.非亲缘异基因骨髓移植治疗儿童白血病[J].中华儿科杂志,2004,42(11):835-839. 被引量:7
  • 2贺其图,时风桐,袁祖正.包头市白血病流行病学调查[J].内蒙古医学杂志,1993,13(2):3-5. 被引量:10
  • 3江倩,陈珊珊,江滨,江浩,丘镜滢,刘艳荣,张艳,秦亚溱,陆颖,黄晓军,陆道培.甲磺酸伊马替尼治疗慢性粒细胞白血病慢性期100例追踪观察[J].中华血液学杂志,2006,27(11):721-726. 被引量:39
  • 4唐正贤 孙秋云 张金桃.上海市金山县11年白血病流行病学调查[J].中华血液学杂志,1994,15(8):430-430.
  • 5National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology: Chronic Myelogenous Leukemia, V. 2. 2008. [ DB/OL]. (2007-10-25). http://www, nccn. org/profes- sionals/physician-gls/f-guidelines, asp#cml.
  • 6Druker BJ, Lee SJ. Chronic myelogenous leukemia//Cancer Prin- ciples and Practice of Oncology. 2007.
  • 7NCCN Clinical Practice Guidelines in oncology TM, Chronic My- elogenous Leukemia, V. 2. 2013. [ DB/OL]. http://www, nccn. org/professionals/physician-gls/f-guidelines, asp#cml.
  • 8Baccarani M, Pileri S, Steegmann JL, et al. Chronic myeloid leu- kemia: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann 0ncol,2012,23 Suppl 7 : vii72-vii77.
  • 9Baccarani M, Cortes J, Pane F, et al. Chronic myeloid leukemia: an update of concepts and management recommendations of the European LeukemiaNet. J Clin Oncol, 2009, 27:6041-6051.
  • 10World Health Organization Classification of Tumors. Pathology and Genetic of Tumors of Haematopoietic and Lymphoid Tissue. 2008.

共引文献100

同被引文献33

引证文献7

二级引证文献31

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部