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曲妥珠单抗和帕妥珠单抗新辅助治疗后 HER2 阳性/激素受体阳性乳腺癌的 HER2DX 基因组检测:来自 PerELISA 试验的相关性分析。

HER2DX genomic test in HER2-positive/hormone receptor-positive breast cancer treated with neoadjuvant trastuzumab and pertuzumab: A correlative analysis from the PerELISA trial.

机构信息

Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy; Istituto Oncologico Veneto, IRCCS, Padova, Italy.

Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.

出版信息

EBioMedicine. 2022 Nov;85:104320. doi: 10.1016/j.ebiom.2022.104320. Epub 2022 Oct 29.

Abstract

BACKGROUND

HER2DX is a prognostic and predictive assay in early-stage HER2-positive breast cancer based on clinical features and the expression of 4 gene signatures (immune, proliferation, luminal differentiation and HER2 amplicon), including ERBB2 mRNA levels. Here, we evaluated the ability of HER2DX to predict efficacy of a de-escalated, chemotherapy-free neoadjuvant regimen in HER2-positive/hormone receptor-positive breast cancer.

METHODS

HER2DX was evaluated on pre-treatment tumour samples from the PerELISA phase II study focused on postmenopausal patients with operable HER2-positive/hormone receptor-positive breast cancer. Patients received 2-weeks of letrozole, and then underwent a re-biopsy for Ki67 evaluation. Patients with endocrine therapy sensitive disease (ESD) (i.e., >20.0% Ki67 relative reduction at week 2) continued letrozole and 5 cycles of trastuzumab and pertuzumab. Primary aim was to test the ability of HER2DX risk-score, HER2DX pCR score and HER2DX ERBB2 mRNA score (as continuous variables and group categories) to predict pathological complete response (pCR) in patients with ESD. Logistic regression and receiver...operator curve (ROC) analysis assessed associations of HER2DX scores with pCR and ESD.

FINDINGS

HER2DX was evaluated in 55 patients (86.0%) enrolled in PerELISA and 40 patients (73.0%) had ESD. The pCR rate in patients with ESD was 22.5% (9/40). In this group, HER2DX pCR score and HER2DX ERBB2 mRNA score were significantly associated with pCR (p.ß=.ß0.008 and p.ß=.ß0.003, univariate logistic regression model; area under ROC [AUC].ß=.ß0.803 and 0.896). The pCR rate in low, medium, and high HER2DX pCR score groups was 7.7% (2/26), 46.2% (6/13) and 100.0% (1/1), respectively. The pCR rate in low, medium, and high HER2DX ERBB2 score groups was 0.0% (0/12), 7.7% (1/13) and 53.3% (8/15), respectively. HER2DX pCR score was also significantly associated with Ki-67 response following 2-weeks of letrozole (p.ß=.ß0.002, univariate logistic regression model; AUC.ß=.ß0.775). The rate of ESD in low, medium, and high HER2DX pCR score groups was 89.7% (26/29), 65.0% (13/20) and 16.7% (1/6), respectively.

INTERPRETATION

HER2DX predicts response following neoadjuvant letrozole in combination with dual HER2 blockade with trastuzumab and pertuzumab in early-stage HER2-positive/hormone receptor-positive breast cancer.

FUNDING

This study received funding from Reveal Genomics.

摘要

背景

HER2DX 是一种基于临床特征和 4 个基因特征(免疫、增殖、腔分化和 HER2 扩增子)表达的早期 HER2 阳性乳腺癌的预后和预测检测方法,包括 ERBB2 mRNA 水平。在这里,我们评估了 HER2DX 在预测 HER2 阳性/激素受体阳性乳腺癌中降阶梯、无化疗新辅助方案疗效方面的能力。

方法

在 PerELISA 二期研究中,对术前肿瘤样本进行了 HER2DX 评估,该研究主要针对可手术的绝经后 HER2 阳性/激素受体阳性乳腺癌患者。患者接受 2 周的来曲唑治疗,然后进行 Ki67 评估的再活检。内分泌治疗敏感疾病(ESD)患者(即,第 2 周 Ki67 相对减少>20.0%)继续接受来曲唑和 5 个周期的曲妥珠单抗和帕妥珠单抗治疗。主要目的是测试 HER2DX 风险评分、HER2DX pCR 评分和 HER2DX ERBB2 mRNA 评分(作为连续变量和分组类别)在 ESD 患者中预测病理完全缓解(pCR)的能力。逻辑回归和接收者...操作者曲线(ROC)分析评估了 HER2DX 评分与 pCR 和 ESD 的关联。

结果

在 PerELISA 中,55 名患者(86.0%)接受了 HER2DX 评估,其中 40 名患者(73.0%)患有 ESD。ESD 患者的 pCR 率为 22.5%(9/40)。在该组中,HER2DX pCR 评分和 HER2DX ERBB2 mRNA 评分与 pCR 显著相关(p.ß=.ß0.008 和 p.ß=.ß0.003,单变量逻辑回归模型;ROC 下面积[AUC].ß=.ß0.803 和 0.896)。低、中、高 HER2DX pCR 评分组的 pCR 率分别为 7.7%(2/26)、46.2%(6/13)和 100.0%(1/1)。低、中、高 HER2DX ERBB2 评分组的 pCR 率分别为 0.0%(0/12)、7.7%(1/13)和 53.3%(8/15)。HER2DX pCR 评分也与来曲唑治疗 2 周后的 Ki-67 反应显著相关(p.ß=.ß0.002,单变量逻辑回归模型;AUC.ß=.ß0.775)。低、中、高 HER2DX pCR 评分组的 ESD 率分别为 89.7%(26/29)、65.0%(13/20)和 16.7%(1/6)。

结论

HER2DX 预测了早期 HER2 阳性/激素受体阳性乳腺癌患者接受新辅助来曲唑联合曲妥珠单抗和帕妥珠单抗双重 HER2 阻断后的反应。

资金来源

本研究得到了 Reveal Genomics 的资助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd26/9626543/c3422f98ead5/gr1.jpg

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