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Importance of biomarkers in glioblastomas patients receiving local BCNU wafer chemotherapy

机译:生物标志物在接受局部BCNU晶片化疗的胶质母细胞瘤患者中的重要性

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BackgroundTo assess the influence of molecular markers with potential prognostic value to groups of patients with newly diagnosed glioblastoma patients were examined: group A with 36 patients (surgical resection plus standard combined chemoradiotherapy) and group B with 36 patients (surgical resection, standard combined chemoradiotherapy plus carmustine wafer implantation).Our aim was to determine chromosomal alterations, methylation status of MGMT, p15, and p16 (CDKN2A) in order to analyse the influence on patient survival time as well as radio- and chemotherapy responses. Promoter hypermethylation of MGMT, p16, and p15 genes were determined by MS-PCR. Comparative genomic hybridisation (CGH) analyses were performed with isolated, labelled DNA of each tumor to detect genetic alterations. ResultsAge of onset of the disease showed a significant effect on overall survival (OS) ( p p =?0.562). Patients with a methylated MGMT promotor showed a significant longer OS compared to those patients with unmethylated MGMT promotor ( p =?0.041). Subgroup analyses revealed that patients with methylated p15 showed a significant shorter OS when administered to group B rather than in group A ( p =?0.0332). In patients additionally treated with carmustine wafer an amplification of 4q12 showed a significant impact on a reduced OS ( p =?0.00835). In group B, a loss of 13q was significantly associated with a longer OS ( p =?0.0364). If a loss of chromosome 10 occurred, patients in group B showed a significantly longer OS ( p =?0.0123). ConclusionA clinical benefit for the widespread use of additional carmustine wafer implantation could not be found. However, carmustine wafer implantation shows a significantly improved overall survival if parts of chromosome 10 or chromosome 13 are deleted. In cases of 4q12 amplification and in cases of a methylated p15 promotor, the use of carmustine wafers is especially not recommended.The MGMT promoter methylation is a strong prognostic Biomarker for benefit from temozolomide and BCNU chemotherapy.
机译:背景为了评估具有潜在预后价值的分子标志物对新诊断的胶质母细胞瘤患者组的影响,检查了:A组36例(手术切除加标准联合放化疗),B组36例(手术切除,标准联合放化疗+联合放化疗)我们的目的是确定MGMT,p15和p16(CDKN2A)的染色体改变,甲基化状态,以便分析对患者生存时间以及放射和化疗反应的影响。通过MS-PCR确定MGMT,p16和p15基因的启动子高甲基化。用每个肿瘤的分离的,标记的DNA进行比较基因组杂交(CGH)分析,以检测遗传改变。结果该疾病的发病年龄对总体生存(OS)有显着影响(p p =?0.562)。与未甲基化MGMT启动子的患者相比,甲基化MGMT启动子的患者的OS明显更长(p =?0.041)。亚组分析显示,与B组相比,B组甲基化的p15患者的OS显着缩短(p =?0.0332)。在接受卡莫司汀片治疗的患者中,4q12的扩增显示出对OS降低的显着影响(p =?0.00835)。在B组中,13q的丧失与更长的OS显着相关(p =?0.0364)。如果发生10号染色体丢失,则B组患者的OS明显更长(p =?0.0123)。结论未发现广泛使用附加卡莫司汀晶片植入的临床益处。但是,如果删除了10号染色体或13号染色体的一部分,则卡莫司汀威化饼植入的总体存活率将显着提高。在4q12扩增的情况下以及在甲基化的p15启动子的情况下,特别不建议使用卡莫司汀片.MGMT启动子甲基化是替莫唑胺和BCNU化疗获益的有力预后生物标志物。

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