Department of Surgery, Iwate Prefectural Iwai Hospital, 17 Odaira, Kozenji, Ichinoseki, 029-0131, Japan.
BMC Cancer. 2024 Sep 2;24(1):1081. doi: 10.1186/s12885-024-12749-x.
Mutated human epidermal growth factor receptor 2 (HER2) is an oncogene with critical pathogenic roles in breast cancer. HER2-low-positive breast cancer is a recently described subtype. We aimed to explore the clinical and molecular characteristics of gastric cancer with low HER2 expression, drawing on recent developments in breast cancer subtypes.
This retrospective study involved 129 patients with HER2-non-amplified gastric cancer treated in Iwate prefectural Iwai Hospital from 2013 to 2019. Tumors were classified as HER2-null or low-positive based on immunohistochemistry score 0 or 1 + or 2 + with HER2 negativity in situ hybridization, respectively. Statistical analyses, including Kaplan-Meier analyses and Cox proportional hazards model were conducted.
Low HER2 expression was present in 26% (33/129) of the patients. Clinicopathological characteristics were not significantly different between the HER2-low and null groups. Kaplan-Meier analysis of overall survival was significantly longer in the HER2-low group than in the HER2-null group (P = 0.01). In multivariate Cox regression analysis, HER2-null status was associated with worse survival (hazard ratio 3.01; 95% confidence interval 1.18-7.65; and P = 0.02).
This study highlights the prognostic importance of low HER2 expression in gastric cancer, similar to that observed in HER2-low-positive breast cancer, and suggests reclassification of gastric cancer to improve personalized treatment. Future studies should elucidate the molecular underpinnings of low HER2 expression in gastric cancer to guide novel therapeutic strategies and improve outcomes.
突变型人类表皮生长因子受体 2(HER2)是一种致癌基因,在乳腺癌中具有关键的致病作用。HER2 低阳性乳腺癌是最近描述的一种亚型。我们旨在借鉴乳腺癌亚型的最新进展,探索低表达 HER2 的胃癌的临床和分子特征。
本回顾性研究纳入了 2013 年至 2019 年在岩手县岩井医院接受治疗的 129 例 HER2 非扩增型胃癌患者。根据免疫组织化学评分 0 或 1+或 2+且原位杂交 HER2 阴性,将肿瘤分别归类为 HER2 阴性或低阳性。进行了统计分析,包括 Kaplan-Meier 分析和 Cox 比例风险模型。
26%(33/129)的患者存在低 HER2 表达。HER2 低表达组和阴性组的临床病理特征无显著差异。总生存的 Kaplan-Meier 分析显示,HER2 低表达组的总生存明显长于 HER2 阴性组(P=0.01)。在多变量 Cox 回归分析中,HER2 阴性状态与较差的生存相关(风险比 3.01;95%置信区间 1.18-7.65;P=0.02)。
本研究强调了低 HER2 表达在胃癌中的预后重要性,与 HER2 低阳性乳腺癌相似,提示对胃癌进行重新分类以改善个体化治疗。未来的研究应阐明胃癌中低 HER2 表达的分子基础,以指导新的治疗策略并改善预后。