...
首页> 外文期刊>Annals of Saudi medicine. >O 6 -methylguanine-DNA methyltransferase promoter methylation and isocitrate dehydrogenase mutation as prognostic factors in a cohort of Saudi patients with glioblastoma
【24h】

O 6 -methylguanine-DNA methyltransferase promoter methylation and isocitrate dehydrogenase mutation as prognostic factors in a cohort of Saudi patients with glioblastoma

机译:O 6 - 近甲基胍-DNA甲基转移酶启动子甲基化和异柠檬酸脱氢酶突变作为胶质母细胞瘤的沙特患者队列的预后因素

获取原文

摘要

BACKGROUND:Treatment of glioblastoma (GB), the most common malignant primary brain tumor in adults, can include alkylating chemo-therapeutic agents. Two molecular biomarkers of treatment response are MGMT (O6-methylguanine-DNA methyltransferase) promoter methylation and IDH (isocitrate dehydrogenase) mutations, which prevent repair of tumor cell DNA damage caused by alkylating chemotherapy. The status of MGMT promoter methylation and IDH mutation are associated with longer survival and a better response to chemotherapy.OBJECTIVE:Assess the prognostic value of MGMT methylation status and IDH mutation in adult Saudi glioblastoma patients.DESIGN:Retrospective, comparative survival analysis.SETTING:Tertiary care center.PATIENTS AND METHODS:The status of the MGMT promoter methylation and IDH mutation was assessed in adult patients diagnosed with GB between 2006 and 2019. A PCR-based assay was used to analyze for methylation of the MGMT promoter. A qualitative assay combining PCR clamping and amplification refractory mutation system technology was used to search for any of the 12 most common mutations in IDH1 and IDH2. Differences in survival were compared between those with and without MGMT promoter methylation and IDH mutation and between other subgroups.MAIN OUTCOME MEASURES:Survival of GB patients relative to MGMT promoter methylation and IDH mutation status.SAMPLE SIZE:146 patients (80 males and 66 females).RESULTS:Of 43 (29.5%) cases tested for MGMT promoter methylation, 14 (32.5%) were positive. Of 65 (44.5%) cases screened for IDH mutation, 6 cases (9.2%) tested positive. The 36-month survival rate was 47% for the MGMT methylated cohort compared to 27% for their unmethylated counterparts. The 18-month survival rate for the IDH-mutant was 75% compared to 48% for their IDH-wildtype counterparts.CONCLUSION:The findings confirm the positive impact of both MGMT promoter methylation and IDH mutation on the overall survival of Saudi GB patients.LIMITATIONS:Single institute study with relatively few tested cases.CONFLICT OF INTEREST:None.
机译:背景:胶质母细胞瘤(GB)的治疗,成人中最常见的恶性原发性脑肿瘤,可包括烷基化化学治疗剂。治疗反应的两个分子生物标志物是MgMt(O6-甲基胍-DNA甲基转移酶)促进剂甲基化和IDH(异柠檬酸脱氢酶)突变,其防止由烷基化化学疗法引起的肿瘤细胞DNA损伤的修复。 MgMT启动子甲基化和IDH突变的状态与更长的存活和更好的化疗反应相关。目的:评估成人沙特胶质母细胞瘤患者的MGMT甲基化状态和IDH突变的预后值。诊断:对比生存分析.Setting:第三级护理中心。分类和方法:在2006年至2019年诊断为GB的成年患者中评估MGMT启动子甲基化和IDH突变的状态。使用基于PCR的测定来分析MGMT启动子的甲基化。组合PCR钳位和扩增耐火突变系统技术的定性测定用于搜索IDH1和IDH2中的12个最常见的突变中的任何一种。比较生存期的差异,在没有MgMT启动子甲基化和IDH突变之间以及其他亚组之间的结果措施:GB患者的生存相对于MGMT启动子甲基化和IDH突变状态。尺寸:146名患者(80名男性和66名女性)。结果:43(29.5%)测试MgMT启动子甲基化的病例,14(32.5%)阳性。 65例(44.5%)病例筛选IDH突变,6例(9.2%)测试阳性。对于其未甲基化的对应物,36个月的存活率为MgMT甲基化队列的47%。其IDH-突变体的18个月生存率为75%,而其IDH野生型对应物的48%相比为48%。结论:调查结果证实了MGMT启动子甲基化和IDH突变对沙特GB患者的总体存活率的积极影响。局限性:单一研究所与相对较少的测试案例进行研究。对兴趣进行感兴趣:无。

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