首页> 外文期刊>Asian Pacific Journal of Cancer Prevention >Ki-67 Can Predict the Response to the Gemcitabine, Oxaliplatin And L-asparaginase Regimen (GELOX) and Prognosis in Patients with Nasal Natural Killer/T-cell Lymphoma
【24h】

Ki-67 Can Predict the Response to the Gemcitabine, Oxaliplatin And L-asparaginase Regimen (GELOX) and Prognosis in Patients with Nasal Natural Killer/T-cell Lymphoma

机译:Ki-67可以预测吉西他滨,奥沙利铂和L-天冬酰胺酶方案(GELOX)的反应以及鼻自然杀伤/ T细胞淋巴瘤患者的预后

获取原文
       

摘要

GELOX (gemcitabine, oxaliplatin and L-asparaginase) regimen showed an impressive result in our previousstudy, but the effect of this new regimen is still dissatisfying for some patients, so it is necessary to identify whichpatients will benefit from this regimen. A total of fifty-one cases with nasal natural killer/T-cell lymphoma receivinginitial GELOX chemotherapy were enrolled in this study. The ki-67 expression detected by immunohistochemistry(IHC) in the specimens ranged from 10% to 90%, with a median value of 70%, so cases higher than the medianvalue (≥70%) were de?ned as high ki-67 expression, and the others were designated as low ki-67 expression.The response rate had no statistical difference between low ki-67 expression group and high ki-67 expressiongroup (P=0.291) though the value in the former group was relatively high. After a median follow-up of 18.03months, the 3-year progression-free survival (PFS) for patients with low ki-67 expression was significantly higherthan those with high ki-67 expression (83.8% vs. 47.9%, P=0.038). In the stage I/II subgroup, 3-year PFS andoverall survival (OS) were statistically higher in the patients with low ki-67 expression than those with high ki-67 expression. Multivariate analysis revealed high ki-67 expression was an independent prognostic factor forPFS. These results suggest that low ki-67 expression can predict a good response of GELOX in these patients,and the combination of ki-67 expression and early stage is helpful to identify an excellent prognosis subgroupfrom patients receiving GELOX in this disease.
机译:GELOX(吉西他滨,奥沙利铂和L-天冬酰胺酶)方案在我们以前的研究中显示了令人印象深刻的结果,但是这种新方案的效果对于某些患者仍然不满意,因此有必要确定哪些患者将从该方案中受益。本研究共纳入了51例接受初始GELOX化疗的鼻自然杀伤/ T细胞淋巴瘤患者。通过免疫组化(IHC)检测到的标本中ki-67表达范围为10%至90%,中位数为70%,因此将高于中位数(≥70%)的病例定义为高ki-67低ki-67表达组和高ki-67表达组之间的响应率无统计学差异(P = 0.291),尽管前一组的值相对较高。在中位随访18.03个月后,ki-67表达低的患者的3年无进展生存期(PFS)明显高于ki-67表达高的患者(83.8%比47.9%,P = 0.038) )。在I / II期亚组中,ki-67表达低的患者的3年PFS和总体生存率(OS)高于ki-67表达高的患者。多变量分析显示,ki-67高表达是PFS的独立预后因素。这些结果表明,ki-67低表达可以预测这些患者的GELOX良好反应,并且ki-67表达与早期阶段的结合有助于从该疾病接受GELOX的患者中识别出良好的预后亚组。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号