Matsubara Junichi, Hirashima Yoshinori, Yamada Yasuhide
Chemotherapy Division, National Cancer Center Research Institute.
Gan To Kagaku Ryoho. 2010 Aug;37(8):1489-96.
We aimed to elucidate the clinical significance of the expressions of HER2, epidermal growth factor receptor (EGFR), insulin-like growth factor receptor (IGF-1R), and vascular endothelial growth factor receptor 1, 2, 3 (VEGF-R1, VEGF-R2, and VEGF-R3) in gastric cancer. The study group comprised 57 patients who had undergone gastrectomy at the National Cancer Center Hospital and subsequently received first-line chemotherapy (S-1 monotherapy [n=29] or irinotecan+cisplatin [n=28]) for recurrent or residual tumors. We performed immunohistochemical analysis of formalin-fixed paraffinembedded specimens of surgically removed primary tumors to determine the expressions of HER2, EGFR, IGF-1R, and VEGFR1 in tumor cells and the expressions of VEGF-R1, VEGF-R2, and VEGF-R3 in tumor stromal vessels. The expressions of HER2 (p=0.017) and IGF-1R (p=0.025) were significantly more common in intestinal type tumors than in diffuse type. The protein expressions did not correlate with tumor response in either chemotherapy-regimen group. Among the patients who underwent S-1 monotherapy, those with cytoplasmic VEGF-R1-positive tumors had significantly shorter progression-free survival (logrank, p=0.017). In the survival analysis of all the patients, coexpression of membranous IGF-1R and VEGF-R3 in stromal vessels was the most significant predictor of poor survival (hazard ratio, 1.82; 95% CI, 1.31-2.63; p<0.001). The results of our study will facilitate more efficient use of molecular targeted agents in patients with gastric cancer.
我们旨在阐明人表皮生长因子受体2(HER2)、表皮生长因子受体(EGFR)、胰岛素样生长因子受体(IGF-1R)以及血管内皮生长因子受体1、2、3(VEGF-R1、VEGF-R2和VEGF-R3)在胃癌中的表达的临床意义。研究组由57例在国立癌症中心医院接受过胃切除术、随后因复发或残留肿瘤接受一线化疗(S-1单药治疗[n=29]或伊立替康+顺铂[n=28])的患者组成。我们对手术切除的原发性肿瘤的福尔马林固定石蜡包埋标本进行免疫组织化学分析,以确定肿瘤细胞中HER2、EGFR、IGF-1R和VEGFR1的表达以及肿瘤间质血管中VEGF-R1、VEGF-R2和VEGF-R3的表达。HER2(p=0.017)和IGF-1R(p=0.025)的表达在肠型肿瘤中比弥漫型肿瘤中更常见。在两个化疗方案组中,蛋白表达均与肿瘤反应无关。在接受S-1单药治疗的患者中,细胞质VEGF-R1阳性肿瘤患者的无进展生存期显著缩短(对数秩检验,p=0.017)。在所有患者的生存分析中,间质血管中膜性IGF-1R和VEGF-R3的共表达是生存不良的最显著预测因素(风险比,1.82;95%置信区间,1.31-2.63;p<0.001)。我们的研究结果将有助于更有效地在胃癌患者中使用分子靶向药物。