下一代肿瘤不可知靶点即将出现
Next-generation tumor-agnostic targets on the horizon.
肿瘤不可知药物开发将肿瘤学重新聚焦于共享的分子依赖性而非组织来源,从而能够针对跨肿瘤的罕见可操作驱动因素进行高效开发。
英文原题:Associations of the HER2DX Genomic Test with Biological and Pathologic Features in HER2-Positive Breast Cancer.
HER2DX反映了HER2+乳腺癌的关键生物学和病理学特征,并独立预测pCR,支持其用于个体化治疗决策。
HER2DX是一种经过验证的基因组检测方法,用于支持早期HER2阳性(HER2+)乳腺癌的治疗决策。它提供三个评分:复发风险、病理完全缓解(pCR)的可能性以及ERBB2 mRNA表达。本研究旨在评估HER2DX与组织病理学特征之间的关联,并评估其与新辅助治疗后pCR的关系。
在西班牙常规诊疗期间(2022年1月至2025年6月),基于可获得的HER2DX结果,对新诊断的I至III期HER2+乳腺癌患者进行了分析。对福尔马林固定、石蜡包埋的肿瘤样本进行了集中式HER2DX检测。组织病理学分析包括肿瘤分级、激素受体状态、组织学亚型、Ki67指数、HER2 IHC评分、间质TIL(肿瘤浸润淋巴细胞)、三级淋巴结构以及空间免疫分布。进行了单变量和多变量logistic回归分析,以确定与新辅助曲妥珠单抗为基础治疗后pCR相关的因素。
共分析410例HER2+肿瘤,250例患者接受了以曲妥珠单抗为基础的新辅助治疗并有可获取的手术结局(36%达到pCR)。HER2DX pCR评分与全部八项组织病理学特征显著相关,而复发风险和ERBB2评分分别与五项和两项相关。TIL与免疫/免疫球蛋白特征相关(r = 0.59),Ki67与增殖特征相关(r = 0.50)。在多变量分析中,HER2DX pCR评分仍是pCR的唯一独立预测因子(OR,1.77;95% confidence interval,1.08-2.97;P = 0.030)。
PURPOSE: HER2DX is a validated genomic assay used to support treatment decisions in early-stage HER2-positive (HER2+) breast cancer. It provides three scores: relapse risk, likelihood of pathologic complete response (pCR), and ERBB2 mRNA expression. This study aimed to evaluate the association between HER2DX and histopathologic features and assess its relationship with pCR after neoadjuvant therapy. EXPERIMENTAL DESIGN: Patients with newly diagnosed stage I to III HER2+ breast cancer were analyzed based on available HER2DX results during routine care in Spain (January 2022-June 2025). Centralized HER2DX testing was performed on formalin-fixed, paraffin-embedded tumor samples. Histopathologic analysis included tumor grade, hormone receptor status, histologic subtype, Ki67 index, HER2 IHC score, stromal tumor-infiltrating lymphocytes (TIL), tertiary lymphoid structures, and spatial immune distribution. Univariate and multivariable logistic regression analyses were conducted to identify factors associated with pCR after neoadjuvant trastuzumab-based therapy. RESULTS: A total of 410 HER2+ tumors were analyzed, and 250 patients received neoadjuvant trastuzumab-based therapy with available surgical outcomes (36% achieved a pCR). HER2DX pCR scores were significantly associated with all eight histopathologic features, whereas relapse risk and ERBB2 scores were associated with five and two, respectively. TIL correlated with the immune/immunoglobulin signature (r = 0.59), and Ki67 with the proliferation signature (r = 0.50). The HER2DX pCR score remained the only independent predictor of pCR in multivariable analysis (OR, 1.77; 95% confidence interval, 1.08-2.97; P = 0.030). CONCLUSIONS: HER2DX reflects key biological and pathologic features of HER2+ breast cancer and independently predicts pCR, supporting its utility for individualized treatment decision-making.
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