Sánchez-Bayona Rodrigo, Martínez-Sáez Olga, Romero-Romero Denys, Seguí Elia, Carcelero Esther, Tolosa Pablo, Soberino Jesús, Alva Manuel, Pascual Tomás, Lema Laura, Garcia-Fructuoso Isabel, Cobos-Fernandez Maria Angeles, Rey Maria, Manso Luis, Aguirre Angela, Madariaga Ainhoa, Sirenko Valeria, González-Deza Cristina, Blasco Paula, Mayhua Astrid, Castillo Oleguer, Galván Patricia, Sanfeliu Esther, Villacampa Guillermo, Buckingham Wesley, Marín-Aguilera Mercedes, Paré Laia, Villagrasa Patricia, Perou Charles M, Maues Julia, Brasó-Maristany Fara, Ciruelos Eva, Prat Aleix
Hospital Universitario 12 de Octubre, Madrid, Spain.
SOLTI Breast Cancer Research Group, Barcelona, Spain.
NPJ Breast Cancer. 2025 Apr 25;11(1):37. doi: 10.1038/s41523-025-00753-8.
In advanced HER2-positive breast cancer, the standard taxane-trastuzumab-pertuzumab (THP) regimen faces competition from new therapies, emphasizing the need for biomarkers to guide treatment. This study evaluates the HER2DX ERBB2 mRNA score as a prognostic predictor, aiming to tailor treatment strategies. We retrospectively analyzed 94 patients treated with the THP regimen between 2010 and 2024. The HER2DX ERBB2 mRNA score was categorized as low (n = 14), medium (n = 20), or high (n = 60), and its correlation with progression-free survival (PFS) and overall survival (OS) was assessed using Cox regression models. The median follow-up was 31.5 months. Patients with ERBB2-high scores had significantly better median PFS (33.9 vs. 10.6 months, hazard ratio [HR] = 0.40, 95% CI: 0.24-0.69, p < 0.001) and OS (not reached vs. 30.8 months, HR = 0.26, 95% CI: 0.13-0.49, p < 0.001) compared to ERBB2-low patients. Based on these findings, further validation of this biomarker in tumor samples from the CLEOPATRA phase III trial is ongoing, which could help optimize treatment strategies in this population.
在晚期人表皮生长因子受体2(HER2)阳性乳腺癌中,标准的紫杉烷-曲妥珠单抗-帕妥珠单抗(THP)方案面临着新疗法的竞争,这凸显了使用生物标志物指导治疗的必要性。本研究评估HER2DX ERBB2 mRNA评分作为一种预后预测指标,旨在制定个性化治疗策略。我们回顾性分析了2010年至2024年间接受THP方案治疗的94例患者。HER2DX ERBB2 mRNA评分被分为低(n = 14)、中(n = 20)或高(n = 60)三组,并使用Cox回归模型评估其与无进展生存期(PFS)和总生存期(OS)的相关性。中位随访时间为31.5个月。与ERBB2低评分患者相比,ERBB2高评分患者的中位PFS(33.9个月对10.6个月,风险比[HR]=0.40,95%置信区间:0.24 - 0.69,p<0.001)和OS(未达到对30.8个月,HR = 0.26,95%置信区间:0.13 - 0.49,p<0.001)显著更好。基于这些发现,正在对来自CLEOPATRA III期试验的肿瘤样本中的这种生物标志物进行进一步验证,这可能有助于优化该人群的治疗策略。