Department of Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Ann Surg Oncol. 2013 Dec;20 Suppl 3:S477-84. doi: 10.1245/s10434-012-2818-0. Epub 2012 Dec 30.
Trastuzumab in association with systemic cytotoxic chemotherapy is the standard of care for patients with advanced HER2-positive gastric carcinoma (GC). However, HER2 as a prognostic factor in GC remains controversial.
HER2 overexpression and amplification was evaluated by immunohistochemistry (IHC) and silver in situ hybridization (SISH) in 2,798 GCs obtained from 2,727 gastrectomy and 71 open/laparoscopic biopsy specimens from patients with peritoneal seeding. Regional heterogeneity was defined as the proportion of tumor cells showing membranous staining in 10-70 % of tumor cells. Genetic heterogeneity was determined by the existence of HER2/CEP17 ratio higher than 2.0 in >5 to <50 % of tumor cells.
In IHC, 184 cases (6.6 %) were 3+ and 44 cases (1.6 %) were 2+. Of 44 HER2 2+ cases, SISH showed HER2 gene amplification in 21 cases (47.7 %), chromosome 17 polysomy in six cases (13.6 %), and genetic heterogeneity in five cases (11.4 %). HER2 positivity found in 7.3 % of GCs was significantly associated with older age, male gender, intestinal histology, upper third in location, higher lymph node stage (p < .002), and advanced AJCC stage (p = .033). Regional heterogeneity of HER2 was closely associated with 2+ (70.5 vs 42.9 % in 3+, p = .001) and diffuse or mixed histologic type (p = .005).
Regional heterogeneity of HER2 expression was closely associated with weak HER2 overexpression (2+) and with diffuse or mixed histology. Polysomy of chromosome 17 would be an important cause of HER2 2+ in IHC. Frequent HER2 positivity observed in GCs with advanced stages suggests that HER2 may be involved in tumor progression and poor prognosis.
曲妥珠单抗联合全身细胞毒性化疗是晚期 HER2 阳性胃癌(GC)患者的标准治疗方法。然而,HER2 作为 GC 的预后因素仍存在争议。
对 2727 例胃切除术后和 71 例剖腹/腹腔镜活检标本中 2798 例 GC 患者的 HER2 过表达和扩增进行免疫组化(IHC)和银原位杂交(SISH)评估。区域异质性定义为 10-70%肿瘤细胞出现膜染色的肿瘤细胞比例。遗传异质性通过存在 HER2/CEP17 比值高于 2.0 的>5-<50%肿瘤细胞来确定。
在 IHC 中,184 例(6.6%)为 3+,44 例(1.6%)为 2+。在 44 例 HER2 2+病例中,SISH 显示 21 例(47.7%)HER2 基因扩增,6 例(13.6%)染色体 17 多倍体,5 例(11.4%)遗传异质性。GC 中发现的 HER2 阳性与年龄较大、男性、肠组织学、上三分之一位置、较高的淋巴结分期(p<.002)和较晚的 AJCC 分期(p=0.033)显著相关。HER2 的区域异质性与 2+(70.5%与 3+的 42.9%,p=0.001)和弥漫或混合组织学类型(p=0.005)密切相关。
HER2 表达的区域异质性与弱 HER2 过表达(2+)和弥漫或混合组织学密切相关。染色体 17 的多倍体可能是 IHC 中 HER2 2+的一个重要原因。在晚期 GC 中观察到的 HER2 阳性率较高提示 HER2 可能参与肿瘤的进展和预后不良。