首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Tubuline, BRCA1, ERCC1, Abraxas, RAP80 mRNA expression, p53/p21 immunohistochemistry and clinical outcome in patients with advanced non small-cell lung cancer receiving first-line platinum-gemcitabine chemotherapy.
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Tubuline, BRCA1, ERCC1, Abraxas, RAP80 mRNA expression, p53/p21 immunohistochemistry and clinical outcome in patients with advanced non small-cell lung cancer receiving first-line platinum-gemcitabine chemotherapy.

机译:接受一线铂-吉西他滨化疗的晚期非小细胞肺癌患者的Tubuline,BRCA1,ERCC1,Abraxas,RAP80 mRNA表达,p53 / p21免疫组化和临床结局。

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BACKGROUND: The aim of this study was to assess the predictive value of tumor expression of nine genes on clinical outcome in patients with advanced NSCLC receiving platinum-gemcitabine chemotherapy. METHODS: Quantitative PCR or immunohistochemistry were used to analyze the expression of beta-tubuline IIA (TUBB2A), beta-tubuline III (TUBB3), BRCA1, ERCC1, Abraxas (ABRX) and RAP80 in mRNA isolated from paraffin-embedded tumor biopsies of 45 NSCLC patients treated as part of a larger observational trial. All patients received first-line platinum-gemcitabine chemotherapy for stage IIIB or IV NSCLC. RESULTS: Median progression-free survival (PFS) was 7 months, overall survival (OS) 12 months. A partial treatment response was found in 14 patients (33%). Patients with low ERCC1 or ABRX expression had a significantly better response to chemotherapy (R=-0.45, p<0.01 for ERCC1; R=-0.40, p=0.016 for ABRX). A significant correlation was found between the individual time for PFS and the expression of both ERCC1 (R=-0.36, p=0.015) and ABRX (R=-0.46, p=0.001). Patients with low ERCC1 expression had a longer OS as compared to patients with high ERCC1 expression (HR=0.26, log-rank p=0.02). CONCLUSIONS: The study confirms tumor expression of ERCC1 as a predictor for clinical outcome in patients with advanced NSCLC receiving platinum-based chemotherapy, and found ABRX expression to be similarly predictive of clinical outcome. Prospective validation is warranted and - if confirmed - non platinum-containing chemotherapy should be explored as the preferred treatment in patients with high ERCC1 or ABRX expression and no activating mutations of EGFR.
机译:背景:本研究的目的是评估九种基因的肿瘤表达对接受铂-吉西他滨化疗的晚期非小细胞肺癌患者临床预后的预测价值。方法:采用定量PCR或免疫组化分析45种石蜡包埋的肿瘤活检组织中的β-微管IIA(TUBB2A),β-微管III(TUBB3),BRCA1,ERCC1,Abraxas(ABRX)和RAP80的表达。 NSCLC患者被视为一项大型观察性试验的一部分。所有患者均接受IIIB或IV期NSCLC一线铂-吉西他滨化疗。结果:中位无进展生存期(PFS)为7个月,总生存期(OS)为12个月。在14例患者中发现了部分治疗反应(33%)。 ERCC1或ABRX表达低的患者对化疗的反应明显更好(ERCC1的R = -0.45,p <0.01; ABRX的R = -0.40,p = 0.016)。发现PFS的各个时间与ERCC1(R = -0.36,p = 0.015)和ABRX(R = -0.46,p = 0.001)的表达之间存在显着相关性。与高ERCC1表达的患者相比,低ERCC1表达的患者的OS更长(HR = 0.26,对数秩p = 0.02)。结论:该研究证实ERCC1的肿瘤表达可作为接受铂类化学疗法的晚期NSCLC患者临床预后的预测指标,并发现ABRX的表达可类似地预测临床预后。有必要进行前瞻性验证,并且-如果得到证实-对于高ERCC1或ABRX表达且无EGFR激活突变的患者,应探索不使用含铂化学疗法作为首选治疗方法。

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