首页> 外文期刊>Cancer: A Journal of the American Cancer Society >O 6-methylguanine-DNA methyltransferase (MGMT) promoter methylation and low MGMT-encoded protein expression as prognostic markers in glioblastoma patients treated with biodegradable carmustine wafer implants after initial surgery followed by radiotherapy with concomitant and adjuvant temozolomide
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O 6-methylguanine-DNA methyltransferase (MGMT) promoter methylation and low MGMT-encoded protein expression as prognostic markers in glioblastoma patients treated with biodegradable carmustine wafer implants after initial surgery followed by radiotherapy with concomitant and adjuvant temozolomide

机译:O 6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化和MGMT编码的蛋白表达低是成胶质母细胞瘤患者的初始手术后继之以伴有辅助性替莫唑胺放疗的胶质母细胞瘤患者的预后标志物

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BACKGROUND: O 6-methylguanine-DNA methyltransferase (MGMT) promoter methylation status was proposed as a prognostic biomarker for patients with glioblastoma. However, the prognostic impact of MGMT in patients with newly diagnosed glioblastoma who receive carmustine-releasing wafers (Gliadel) along with temozolomide (TMZ) is still unknown. METHODS: MGMT promoter methylation status and protein expression were analyzed in formalin-fixed, paraffin-embedded tumor specimens obtained from 111 French patients with newly diagnosed glioblastoma. Patients received the Gliadel wafers followed by radiotherapy plus concomitant and adjuvant TMZ chemotherapy while they were enrolled in a French multicenter prospective study. RESULTS: For the whole cohort, the median overall survival (OS) was 17.5 months, and the progression-free survival was 10.3 months. Patients with tumors that harbored MGMT methylation had a significantly longer OS compared with patients who had wild-type MGMT (21.7 months vs 15.1 months; P =.025). Similarly, patients who had low MGMT protein expression (≤15%) had a significantly improved OS compared with patients who had high MGMT expression (27.0 months vs 15.1 months; P =.021). The extent of resection was the strongest clinical predictor of outcome. In multivariate Cox models that were adjusted for sex, performance status, and extent of surgery, both MGMT methylation and protein expression were identified as independent prognosticators, and the finding was validated internally using a bootstrap resampling technique. Discrepancies were identified between protein expression and MGMT methylation status, thus suggesting that the 2 assays probably assess different biologic features. CONCLUSIONS: MGMT promoter methylation status and low MGMT expression both were identified as positive prognosticators in patients with newly diagnosed glioblastoma who underwent surgical resection and received Gliadel wafer implants followed by adjuvant radiotherapy and concomitant oral TMZ chemotherapy (the Stupp protocol). Cancer 2012.
机译:背景:O 6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化状态被提议作为胶质母细胞瘤患者的预后生物标志物。然而,MGMT对接受卡莫司汀片(替米唑胺)(TMZ)接受卡莫司汀片治疗的新诊断成胶质母细胞瘤患者的预后影响仍然未知。方法:在111例法国新诊断成胶质细胞瘤患者中,用福尔马林固定,石蜡包埋的肿瘤标本分析了MGMT启动子的甲基化状态和蛋白表达。患者参加了法国的多中心前瞻性研究,接受了Gliadel薄酥饼,然后接受放射治疗以及伴随和辅助的TMZ化疗。结果:对于整个队列,中位总生存期(OS)为17.5个月,无进展生存期为10.3个月。与野生型MGMT相比,具有MGMT甲基化的肿瘤患者的OS明显更长(21.7个月vs 15.1个月; P = .025)。同样,MGMT蛋白表达水平低(≤15%)的患者与MGMT蛋白表达水平高的患者相比,OS显着改善(27.0个月vs 15.1个月; P = .021)。切除的程度是最强的临床预后指标。在针对性别,行为状态和手术程度进行了调整的多变量Cox模型中,MGMT甲基化和蛋白质表达均被确定为独立的预后指标,并且使用自举重采样技术在内部验证了这一发现。确定了蛋白质表达和MGMT甲基化状态之间的差异,因此表明这两种测定法可能评估了不同的生物学特征。结论:MGMT启动子甲基化状态和MGMT低表达均被确定为新诊断成胶质母细胞瘤的患者的阳性预后,这些患者接受了手术切除并接受了Gliadel晶片植入物,并辅以放射疗法和口服TMZ化疗(Stupp方案)。癌症2012。

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