Division of Hematology-Oncology, Rush University Medical Center, Chicago, Illinois, USA.
Department of Internal Medicine, Rush University Medical Center, Chicago, Illinois, USA.
Cancer Med. 2022 Dec;11(24):4954-4965. doi: 10.1002/cam4.4843. Epub 2022 Jun 22.
Accurate diagnostic biomarker testing is crucial to treatment decisions in breast cancer. Biomarker testing is performed on core needle biopsies (CNB) and is often repeated in the surgical specimen (SS) after resection. As differences between CNB and SS testing may alter treatment decisions, we evaluated concordance between CNB and SS as well as associated changes in treatment and clinical outcomes.
We performed a retrospective analysis of breast cancer patients at our institution between January 2010 and May 2020. Concordance between CNB and SS was assessed for estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) by immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH). Survival in patients, including recurrence, metastatic recurrence, and death, were assessed using chi-squared likelihood ratio.
In total, 961 patients met eligibility criteria. Concordance, minor discordance, total concordance (concordance plus minor discordance), and major discordance between CNB and SS were reported for ER (87.7%, 9.2%, 90.8%, and 2.9%), PR (58.1%, 29.1%, 87.2%, and 12.8%), and HER2 IHC (52.5%, 20.9%, 73.4%, 26.6%), respectively. HER2 FISH concordance and major discordance were 58.5% and 1.2%, respectively. Of major discordance, ER (48.2%, p < 0.001) and HER2 FISH (50.0%) led to more management changes than HER2 IHC (2.4%, p = 0.04) and PR (1.6%, p = 0.10). Patients with ER major discordance had increased risk of death (6.7% concordance vs. 22.2% major discordance, p = 0.004).
Overall, retesting ER and HER2 was more clinically beneficial than retesting PR. To aid decision-making and minimize healthcare costs, we propose patient-centered guidelines on retesting biomarker profiles.
准确的诊断生物标志物检测对乳腺癌的治疗决策至关重要。生物标志物检测是在核心针活检(CNB)上进行的,并且通常在切除后的手术标本(SS)中重复进行。由于 CNB 和 SS 检测之间的差异可能会改变治疗决策,因此我们评估了 CNB 和 SS 之间的一致性以及治疗和临床结果的相关变化。
我们对 2010 年 1 月至 2020 年 5 月期间我院的乳腺癌患者进行了回顾性分析。通过免疫组织化学(IHC)和荧光原位杂交(FISH)评估 CNB 和 SS 之间雌激素受体(ER)、孕激素受体(PR)和人表皮生长因子受体 2(HER2)的一致性。使用卡方似然比评估患者的生存情况,包括复发、转移性复发和死亡。
共有 961 名患者符合入选标准。报告了 CNB 和 SS 之间 ER(87.7%、9.2%、90.8%和 2.9%)、PR(58.1%、29.1%、87.2%和 12.8%)和 HER2 IHC(52.5%、20.9%、73.4%和 26.6%)的一致性、微小差异、总一致性(一致性加微小差异)和主要差异。HER2 FISH 的一致性和主要差异分别为 58.5%和 1.2%。在主要差异中,ER(48.2%,p<0.001)和 HER2 FISH(50.0%)比 HER2 IHC(2.4%,p=0.04)和 PR(1.6%,p=0.10)导致更多的治疗变化。ER 主要差异的患者死亡风险增加(一致性为 6.7%,主要差异为 22.2%,p=0.004)。
总体而言,与重新检测 PR 相比,重新检测 ER 和 HER2 更具有临床益处。为了帮助决策并降低医疗保健成本,我们提出了以患者为中心的重新检测生物标志物谱的指南。