Department of Medicine, Sungkyunkwan University Samsung Medical Center, Seoul, Korea.
Cancer Res Treat. 2010 Jun;42(2):101-6. doi: 10.4143/crt.2010.42.2.101. Epub 2010 Jun 30.
The aim of this study was to determine whether the ERCC1 expression is effective to predict the clinical outcomes of patients with advanced gastric cancer (AGC) and who were treated with cisplatin-based first-line chemotherapy.
A total of 89 measurable AGC patients received cisplatin and capecitabine, with or without epirubicin, as a part of a randomized phase II study. Patients were included for the current molecular analysis if they had received two or more cycles of chemotherapy, their objective tumor responses were measured and if their paraffin-embedded tumor samples were available. The ERCC1 expression was examined by performing immunohistochemical (IHC) staining, and the patients were divided into two groups (positive or negative) according to the presence of IHC staining of the tumor cell nuclei.
Of the 32 eligible patients, 21 patients (66%) had tumor with a positive expression of ERCC1 and the remaining 11 patients had tumor with a negative ERCC1-expression. The ERCC1-negative patients achieved a higher response rate than that of the ERCC1-positive patients (44% vs. 28%, respectively), although the difference was not statistically significant (p=0.42). The median survival time for the all patients was 14.6 months (95% CI: 13.6 to 15.6 months). The one-year survival rate was similar for the ERCC1-negative patients (61%) and the ERCC1-positive patients (70%).
In the current study, the tumor ERCC1 expression by IHC staining could not predict the clinical response or survival of AGC patients who were treated with cisplatin-based first-line chemotherapy. The ERCC1 protein expression does not appear to be a useful tool for the selection of tailored chemotherapy for these patients.
本研究旨在确定 ERCC1 表达是否能有效预测接受顺铂为基础的一线化疗的晚期胃癌(AGC)患者的临床结局。
共有 89 例可测量的 AGC 患者接受顺铂和卡培他滨治疗,联合或不联合表柔比星,作为一项随机 II 期研究的一部分。如果患者接受了两个或更多周期的化疗,客观肿瘤反应可测量,并且有石蜡包埋的肿瘤样本,则将其纳入当前的分子分析。通过免疫组织化学(IHC)染色检查 ERCC1 表达,并根据肿瘤细胞核的 IHC 染色存在将患者分为两组(阳性或阴性)。
在 32 名合格的患者中,21 名(66%)患者的肿瘤 ERCC1 表达阳性,其余 11 名患者的肿瘤 ERCC1 表达阴性。与 ERCC1 阳性患者相比(分别为 44%和 28%),ERCC1 阴性患者的反应率更高,但差异无统计学意义(p=0.42)。所有患者的中位生存时间为 14.6 个月(95%CI:13.6 至 15.6 个月)。ERCC1 阴性患者的 1 年生存率与 ERCC1 阳性患者相似(分别为 61%和 70%)。
在本研究中,通过 IHC 染色检测肿瘤 ERCC1 表达不能预测接受顺铂为基础的一线化疗的 AGC 患者的临床反应或生存。ERCC1 蛋白表达似乎不是为这些患者选择针对性化疗的有用工具。