Institute of Pathology, Technische Universität München, Trogerstr. 18, 81675 München, Germany.
Eur J Cancer. 2009 Dec;45(18):3326-35. doi: 10.1016/j.ejca.2009.09.021. Epub 2009 Oct 12.
We evaluated DNA polymorphisms in genes related to DNA repair, cell-cycle control and tumour microenvironment to determine possible associations with response and survival in neoadjuvant-treated gastric cancer patients.
One hundred and seventy eight patients who received platinum/5FU-based chemotherapy were genotyped for 10 polymorphisms in nine genes (ERCC1: Asn118Asn, C > T; ERCC1: 8092C > A; TP53: Arg72Pro, G < C; cyclinD1: Pro241Pro, G > A; STK15: Phe31Ile, A > T; VEGF: 936C > T; TNF-alpha: -308G > A; interleukin-1b (IL-1B): -511C >T; IL-1 receptor antagonist (IL-1RN): variable tandem repeat; IL-8: -251T>A). Genotypes were correlated with histopathological and clinical response and overall (OS) and progression-free survival (PFS).
Only the cyclinD1 genotypes were associated with clinical response (P(x)(2)=0.044). Significantly worse survival rates were noted in patients homozygous for the G-allele as compared to patients with the AG or AA genotypes of the cyclinD1 polymorphism (OS: P(log-rank) = 0.024; PFS: P(log-rank)=0.007) and in patients homozygous for the short allele compared to all other genotypes at the IL-1RN polymorphic locus (OS: P(log-rank) = 0.026; PFS: P(log-rank) = 0.013). The combination of both unfavourable genotypes demonstrated strong prognostic relevance (OS: P(log-rank) = 0.006; PFS: P(log-rank) = 0.001). Multivariate analysis for OS in the group of completely resected patients (n = 139) revealed statistical significance for ypM (P < 0.001), histopathological response (P < 0.001) and the combined cyclinD1/IL-1RN genotypes (P = 0.043).
The cyclinD1 and IL-1RN polymorphisms were associated with survival. The combination of specific cyclinD1 and IL-1RN genotypes showed a particular prognostic relevance and should be considered an independent prognostic marker for neoadjuvant-treated gastric cancer patients.
我们评估了与 DNA 修复、细胞周期控制和肿瘤微环境相关的基因中的 DNA 多态性,以确定其与新辅助化疗治疗的胃癌患者的反应和生存之间的可能关联。
178 名接受铂类/5FU 为基础化疗的患者接受了 9 个基因中的 10 个基因(ERCC1:Asn118Asn,C>T;ERCC1:8092C>A;TP53:Arg72Pro,G>C;cyclinD1:Pro241Pro,G>A;STK15:Phe31Ile,A>T;VEGF:936C>T;TNF-α:-308G>A;白细胞介素-1b(IL-1B):-511C>T;白细胞介素-1 受体拮抗剂(IL-1RN):可变串联重复;IL-8:-251T>A)的 10 个多态性的基因分型。将基因型与组织病理学和临床反应以及总生存期(OS)和无进展生存期(PFS)相关联。
只有 cyclinD1 基因型与临床反应相关(P(x)(2)=0.044)。与 cyclinD1 多态性的 AG 或 AA 基因型患者相比,纯合 GG 基因型患者的生存率明显较差(OS:P(log-rank)=0.024;PFS:P(log-rank)=0.007),与 IL-1RN 多态性位点的短等位基因纯合患者相比,所有其他基因型患者的生存率也较差(OS:P(log-rank)=0.026;PFS:P(log-rank)=0.013)。两种不利基因型的组合具有很强的预后相关性(OS:P(log-rank)=0.006;PFS:P(log-rank)=0.001)。在完全切除患者组(n=139)中进行的 OS 的多变量分析显示,ypM(P<0.001)、组织病理学反应(P<0.001)和 cyclinD1/IL-1RN 基因型的组合(P=0.043)具有统计学意义。
cyclinD1 和 IL-1RN 多态性与生存相关。特定 cyclinD1 和 IL-1RN 基因型的组合显示出特定的预后相关性,应被视为新辅助化疗治疗的胃癌患者的独立预后标志物。