乳腺癌的临床病理特征与2018年美国临床肿瘤学会/美国病理学家学院荧光原位杂交第3组(人表皮生长因子受体2染色体17着丝粒比率<2.0,平均人表皮生长素受体2拷贝数≥6.0)乳腺癌。

Diane Wilcock, Deepika Sirohi, Daniel Albertson, Allison S Cleary, Joshua F Coleman, Jolanta Jedrzkiewicz, Jonathan Mahlow, Ana L Ruano, H Evin Gulbahce
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引用次数: 0

摘要

上下文。--:美国临床肿瘤学会/美国病理学家学院2018年人类表皮生长因子受体2(HER2)测试指南的更新包括具有HER2与17号染色体着丝粒(CEP17)比率小于2.0和HER2拷贝数6.0或更大的荧光原位杂交(FISH)组(第3组),这需要对HER2免疫组织化学(IHC)进行综合审查。目的:评估第3组患者的临床病理特征,并确定检查后与HER2阳性状态相关的特征。设计。--:确定了2019年1月至2022年6月期间提交的HER2 FISH病例,并获得了相关的临床病理信息。结果。--:142例HER2 FISH病例(1.6%)为第3组。52例(36.6%)IHC阴性(0/1+),3例(2.8%)IHC阳性(3+),86例(60.6%)IHC-为2+。第二位评审员在目标区域对带注释的IHC 2+载玻片进行了复述,其中86张(18.6%)中有16张的HER2:CEP17比率小于2.0,HER2拷贝数为4.0或更大至小于6.0(HER2阴性)。在综合IHC/FISH审查后,142例中有74例(52.1%)被归类为HER2阳性。检查后,HER2阳性病例的HER2拷贝数/细胞高于HER2阴性病例。IHC2+病例的染色程度和强度与基因扩增水平无关。20%的HER2阳性患者获得了病理学完全缓解。结论。--:第3组病例中约有一半在进一步检查后被归类为HER2阳性。HER2阳性病例的病理学完全缓解率低于第1组(HER2:CEP17比值≥2.0;HER2拷贝数≥4.0)患者的预期。IHC靶向FISH重新计数可能是多余的,并且可能导致一些患者被归类为HER2阴性,从而导致靶向治疗被拒绝。
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Clinicopathologic Features of 2018 American Society of Clinical Oncology/College of American Pathologists Fluorescence In Situ Hybridization Group 3 Breast Carcinoma (Human Epidermal Growth Factor Receptor 2 Chromosome 17 Centromere Ratio <2.0 and Average Human Epidermal Growth Factor Receptor 2 Copy Number ≥6.0).

Context.—: The American Society of Clinical Oncology/College of American Pathologists 2018 update of the human epidermal growth factor receptor 2 (HER2) testing guideline includes a fluorescence in situ hybridization (FISH) group with a HER2 to chromosome 17 centromere (CEP17) ratio less than 2.0 and HER2 copy number 6.0 or greater (group 3), which requires integrated review of HER2 immunohistochemistry (IHC).

Objective.—: To assess the clinicopathologic features of group 3 patients and determine features associated with HER2-positive status after workup.

Design.—: Cases submitted for HER2 FISH between January 2019 and June 2022 were identified, and relevant clinicopathologic information was obtained.

Results.—: One hundred forty-two HER2 FISH cases (1.6%) were group 3. In 52 cases (36.6%) IHC was negative (0/1+), in 3 (2.8%) IHC was positive (3+), and in 86 (60.6%) IHC was 2+. Annotated IHC 2+ slides were recounted by a second reviewer in targeted areas, where 16 of 86 (18.6%) had a HER2:CEP17 ratio less than 2.0 and a HER2 copy number of 4.0 or greater to less than 6.0 (HER2 negative). After combined IHC/FISH review, 74 of 142 (52.1%) were classified as HER2 positive. HER2 copy number/cell was higher in HER2-positive compared with HER2-negative cases after the workup. The extent and intensity of staining in IHC 2+ cases did not correlate with the level of gene amplification. Twenty percent of HER2-positive patients achieved pathologic complete response.

Conclusions.—: About half of group 3 cases were classified as HER2 positive after additional workup. Pathologic complete response rates in HER2-positive cases were lower than expected for group 1 (HER2:CEP17 ratio ≥2.0; HER2 copy number ≥4.0) patients. IHC-targeted FISH recounts may be redundant and may potentially lead to classification of some patients as HER2 negative, resulting in withholding of targeted therapy.

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