Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55906, USA.
Department of Pathology, University of New Mexico Health Sciences Cancer Center, Albuquerque, NM, 87131, USA.
Hum Pathol. 2023 Jul;137:94-101. doi: 10.1016/j.humpath.2023.04.009. Epub 2023 Apr 23.
HER2 (ERBB2) overexpression and/or HER2 gene amplification has been well established in several tumors types and when present HER2 directed therapy may be to be efficacious. While recent findings suggests that HER2 overexpression and HER2 amplification are a relatively common in serous endometrial carcinoma, similar data regarding clear cell endometrial carcinoma (CCC) is difficult to interpret due to issues such as diagnostic criteria, sample type and HER2 interpretation criteria. Our goals were to study HER2 expression and HER2 copy number status in hysterectomy specimens from a large series of patients with pure CCC to determine the frequency of HER2 overexpression and HER2 amplification and evaluate applicability of current HER2 interpretation criteria. Pure CCC specimens derived from hysterectomy specimens from 26 patients were identified. All diagnoses were confirmed by two gynecologic pathologists. Immunohistochemistry for HER2 protein and fluorescence in situ hybridization (FISH) studies for HER2 were performed on whole-slide sections from all cases. Results were interpreted according to the 2018 ASO/CAP HER2 guidelines for breast cancer and International Society of Gynecologic Pathologists (ISGyP) HER2 guidelines for serous endometrial carcinoma. Additional testing was performed when indicated by the guidelines. HER2 expression by immunohistochemistry was 3+ in 4% and 0% of cases, and 2+ in 46% and 52% of cases, by 2018 ASCO/CAP and ISGyP criteria, respectively, while the remaining cases were negative. HER2 testing by FISH showed a positive result in 27% of tumors with 2018 ASCO/CAP guidelines, while 23% were positive with the ISGyP criteria. Our findings indicate that HER2 overexpression and HER2 amplification occur in a subset of CCC. Therefore, additional study into the potential benefit of HER2 targeted therapy in patients with CCC is warranted.
HER2(ERBB2)过表达和/或 HER2 基因扩增已在多种肿瘤类型中得到证实,当存在时,HER2 靶向治疗可能有效。虽然最近的研究结果表明,HER2 过表达和 HER2 扩增在浆液性子宫内膜癌中相对常见,但由于诊断标准、样本类型和 HER2 解读标准等问题,关于透明细胞子宫内膜癌(CCC)的类似数据难以解释。我们的目标是研究大量纯 CCC 患者子宫切除标本中 HER2 表达和 HER2 拷贝数状态,以确定 HER2 过表达和 HER2 扩增的频率,并评估当前 HER2 解读标准的适用性。从 26 例患者的子宫切除标本中鉴定出纯 CCC 标本。所有诊断均由两名妇科病理学家确认。对所有病例的全切片进行 HER2 蛋白免疫组化和 HER2 荧光原位杂交(FISH)研究。结果根据 2018 年 ASCO/CAP 乳腺癌 HER2 指南和国际妇科病理学家协会(ISGyP)浆液性子宫内膜癌 HER2 指南进行解读。根据指南需要时进行额外测试。根据 2018 年 ASCO/CAP 和 ISGyP 标准,免疫组化 HER2 表达在 4%和 0%的病例中为 3+,在 46%和 52%的病例中为 2+,而其余病例为阴性。根据 FISH 检测,2018 年 ASCO/CAP 指南中 27%的肿瘤检测结果为阳性,而 ISGyP 标准中 23%的肿瘤检测结果为阳性。我们的研究结果表明,HER2 过表达和 HER2 扩增发生在 CCC 的一个亚组中。因此,需要进一步研究 HER2 靶向治疗在 CCC 患者中的潜在获益。