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CD_(117)在急性非淋巴细胞性白血病细胞的表达与患者生存时间的关系 被引量:4

A study on the expression CD_(117) in acute nonlymphoid leukemia and its impacts on survial duration
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摘要 目的 观察CD117在急性非淋巴细胞性白血病 (ANLL)细胞中的表达 ,评价其对白血病患者生存时间判断方面的价值。方法 采用流式细胞仪对 6 6例ANLL患者的白血病细胞进行分析。观察CD117阳性和阴性患者的预后 ,并做多因素分析。结果  6 6例ANLL患者中 ,41例表达CD117,CD117在ANLL患者中各亚型的表达差异无显著性 (P >0 .0 5 )。CD117阳性患者完全缓解 (CR)率低(43 9% ) ,CD117阴性患者CR率高 (72 0 % ) (P <0 .0 5 )。CD117阳性患者生存时间短 (196d) ,CD117阴性患者生存时间长 (30 2d) (Log Rank检验P =0 .0 0 12 )。将年龄、性别、WBC、缓解、复发、CD117阳性分别引入Cox模型和logistic回归进行多参数分析 ,结果显示CD117可能是影响ANLL患者预后的一个因素(P <0 .0 5 )。 Objective To explore the expression of CD 117 on blasts of ANLL and its impacts on survial duration of patients with ANLL. Methods Single color flow cytometry was performed to examine CD 117 expression in 66 patients with ANLL. Prognosis of a CD 117 positive and CD 117 negative group was observed and prognostic factors were analysed. Results Of the 66 patients with ANLL,41 had CD 117 expression. There was no correlation between CD 117 expression and FAB subtypes. A lower complete remission (CR) rate ( P <0.05) and shorter survival duration were found in the CD 117 positive patients with ANLL (Log Rank test P =0.001 2) than those in the CD 117 negative. CD 117 negative group had higher cumulative survival, lower cumulative hazard than CD 117 positive group .Multivariation analysis, including age, sex, WBC count, CD 117 expression, remission and relapse, demonstrated that the expression of CD 117 in ANLL patients may be an independent prognostic factor. Conclusion ANLL patients with positive CD 117 expression had a poor prognosis.
出处 《中华内科杂志》 CAS CSCD 北大核心 2000年第7期461-463,共3页 Chinese Journal of Internal Medicine
关键词 非淋巴细胞性白血病 存活率 基因表达 CD117 Leukemia, nonlymphocytic, acute Proto oncogene proteins c kit Survial rate
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参考文献2

  • 1艾辉胜,现代白血病学,1997年,164页
  • 2张之南,血液病诊断及疗效标准,1991年,190页

同被引文献26

  • 1时昊,张志瑢,肖爱琴,朱锋,张日.c-kit受体与其他髓系膜抗原标志物对急性非淋巴细胞白血病诊断价值的比较[J].中华内科杂志,2005,44(5):384-385. 被引量:12
  • 2李睿娟,龚凡杰,张广森.塞来昔布对K562白血病细胞的细胞毒作用及与伊马替尼的协同效应[J].中华医学杂志,2006,86(20):1417-1420. 被引量:2
  • 3Nakayama S, Nagamura-Inoue T, Yokoyama K, et al. Cytogenetic remissions induced by interferon alpha and imatinib mesylate are immunologically distinct in chronic myeloid leukemia. Int J Hematol, 2007 ;86 (3) :208 - 211.
  • 4Giles FJ, Kantarjian HM, Bekele BN, et al. Bone marrow cyclooxygenase-2 revels are elevated in chronic-phase chronic myeloid leukaemia and are associated with reduced survival. Br J Haematol, 2002 ;119 ( 1 ) :38 -45.
  • 5Peng HL, Zhang GS, Liu JH, et al. Dup-697, a specific COX-2 inhibitor, suppresses growth and induces apoptosis on K562 leukemia cells by cell-cycle arrest and caspase-8 activation. Ann Hematol, 2008 ;87 (2) : 121 - 129.
  • 6Arunasree KM, Roy KR, Anilkumar K, et al. Imatinib-resistant K562 cells are more sensitive to celecoxib, a selective COX-2 inhibitor: role of COX-2 and MDR-1. Leuk Res, 2008;32(6) :855 - 864.
  • 7Bonifazi F, de Vivo A, Rosti G,et al. Chronic myeloid leukemia and interferon-alpha: a study of complete cytogenetic responders. Blood,2001 ;98 (10) :3074 - 3081.
  • 8Kantarjian HM, O'Brien S, Cortes JE, et al. Complete cytogenetic and molecular responses to interferon-alpha-based therapy for chronic myelogenous leukemia are associated with excellent long- term prognosis. Cancer, 2003 ;97 (4) : 1033 - 1041.
  • 9Hehlmann R, Berger U, Pfirrmann M, et al. Drug treatment is superior to allografting as first-line therapy in chronic myeloid leukemia. Blood, 2007 ;109( 11 ) :4686 -4692.
  • 10Miele L. The biology of cyclins and cyclins-dependent protein kinases : an introduction. Methods Mol Biol, 2004 ;285:3 - 21.

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