Muñoz Javier, Nucera Sabrina, Rubira Garcia Nuria, Cebrecos Isaac, Oses Gabriela, Ganau Sergi, Sanfeliu Esther, Jares Pedro, Marín-Aguilera Mercedes, Galván Patricia, Brasó-Maristany Fara, Martínez-Sáez Olga, Cascos Enric, Font Carme, Schettini Francesco
Medical Oncology Department, Hospital Clinic of Barcelona, C. Villaroel 170, 08036, Barcelona, Spain.
Translational Genomics and Targeted Therapies in Solid Tumors Group, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), C. Villaroel 170, 08036, Barcelona, Spain; Department of Human Pathology "G. Barresi", University of Messina, 98131, Messina, Italy.
Breast. 2025 Jun;81:104465. doi: 10.1016/j.breast.2025.104465. Epub 2025 Apr 4.
We present the first documented oncologic case of a type I Kounis syndrome (KS) following paclitaxel administration, in a very young patient with HER2-positive(+) early-stage breast cancer (BC). KS is a relatively rare acute coronary syndrome triggered by anaphylactic or hypersensitivity reactions, of which there is limited awareness among healthcare providers. It is subdivided in four subtypes depending on cardiac artery medical history. While no established management guidelines exist, its treatment requires addressing severe infusion reactions while ensuring proper myocardial perfusion. We hereby illustrate its successful acute management and report on how tumor genomics through the novel HER2DX assay helped re-defining the entire neo/adjuvant oncologic strategy. HER2DX integrates tumor size and nodal involvement with 27 genes' expression data tracking four biological BC-related and immunologic signatures so to estimate a prognostic and a predictive score. This report demonstrates how clinical and genomic data can be effectively integrated to optimize therapeutic decisions in HER2+ BC, offering a model for personalized care also in atypical and complex cases.
我们报告了首例有记录的在一名非常年轻的HER2阳性早期乳腺癌(BC)患者中,使用紫杉醇后发生的I型库尼斯综合征(KS)肿瘤病例。KS是一种由过敏或超敏反应引发的相对罕见的急性冠状动脉综合征,医疗服务提供者对其认识有限。根据冠状动脉病史,它可分为四个亚型。虽然目前尚无既定的管理指南,但其治疗需要在确保适当心肌灌注的同时应对严重的输液反应。我们在此展示了其成功的急性管理,并报告了通过新型HER2DX检测进行的肿瘤基因组学如何有助于重新定义整个新辅助/辅助肿瘤治疗策略。HER2DX将肿瘤大小和淋巴结受累情况与27个基因的表达数据相结合,追踪四种与BC相关的生物学和免疫特征,从而估算出一个预后和预测评分。本报告展示了如何有效整合临床和基因组数据,以优化HER2 + BC的治疗决策,也为非典型和复杂病例的个性化护理提供了一个模型。