Jensen Maj-Britt, Nielsen Torsten O, Bartlett John, Lænkholm Anne-Vibeke, Shepherd Lois, Ejlertsen Bent
Danish Breast Cancer Cooperative Group, Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Department of Pathology and Laboratory Medicine, Genetic Pathology Evaluation Centre, University of British Columbia, Vancouver, Canada.
NPJ Breast Cancer. 2025 Mar 10;11(1):26. doi: 10.1038/s41523-025-00738-7.
NCIC-CTG MA.5 and DBCG 89D are symmetrically designed randomized trials comparing adjuvant cyclophosphamide, epirubicin, and fluorouracil with cyclophosphamide, methotrexate, and fluorouracil in high-risk breast cancer patients. In a joint analysis we evaluate the predictive value in terms of anthracycline benefit of molecular subtyping by PAM50. A statistically significant interaction (P = 0.008) between continuous Risk of Recurrence (ROR) score and treatment regimen is evident, translating into a clear distinct treatment effect according to ROR score category with HR 0.51 for ROR score ≥ 72 and HR 1.10 for ROR score < 52 (P = 0.004). The analysis provides evidence of the benefit from anthracycline in HER2-enriched subtype; for patients with discordance of HER2 subtype and clinical HER2 status, HER2-enriched subtype was predictive of anthracycline benefit whereas clinical HER2 positive status was not. Anthracycline-based adjuvant chemotherapy may safely be withheld for patients with a low ROR score while the benefit increases with increasing ROR score.
NCIC-CTG MA.5和DBCG 89D是对称设计的随机试验,比较了高危乳腺癌患者中辅助性环磷酰胺、表柔比星和氟尿嘧啶与环磷酰胺、甲氨蝶呤和氟尿嘧啶的疗效。在一项联合分析中,我们根据PAM50分子亚型评估了蒽环类药物获益方面的预测价值。连续复发风险(ROR)评分与治疗方案之间存在显著的统计学交互作用(P = 0.008),这意味着根据ROR评分类别有明显不同的治疗效果,ROR评分≥72时HR为0.51,ROR评分<52时HR为1.10(P = 0.004)。该分析提供了蒽环类药物在HER2富集亚型中获益的证据;对于HER2亚型与临床HER2状态不一致的患者,HER2富集亚型可预测蒽环类药物的获益,而临床HER2阳性状态则不能。对于ROR评分低的患者,可以安全地不进行基于蒽环类药物的辅助化疗,而获益会随着ROR评分的增加而增加。