Surgical Interest of an Accurate Real-World Prediction of Primary Systemic Therapy Response in HER2 Breast Cancers.
Jose Ignacio Sánchez-MéndezMónica HorstmannNieves MéndezLaura FríasElisa MorenoLaura YébenesMᵃ José RocaAlicia HernándezCovadonga MartíPublished in: Cancers (2023)
Human epidermal growth factor receptor 2 (HER2)-enriched breast cancers (BC) present the highest rates of pathological response to primary systemic therapy (PST), but they are also the ones that tend to be larger at diagnosis, with microcalcifications and, often, with axillary involvement. If we do not have a reliable method to predict the degree of response, we may not be able to transfer the benefits of PST to surgery. The post-PST surgery planning is guided by the findings in the magnetic resonance imaging (MRI), whose predictive capacity, although high, is far from optimal. Thus, it seems interesting to find other variables to improve it. A retrospective observational study including women with HER2 BC treated with PST and further surgery was conducted. Information regarding clinical, radiological, and histopathological variables was gathered from a total of 132 patients included. Radiological complete response (rCR) was achieved in 65.9% of the sample, and pathological complete response (pCR), according to Miller and Payne criteria, in 58.3% of cases. A higher Ki67 value, the absence of Hormonal Receptors expression, and an rCR was significantly related to a pCR finding. This information impacts directly in surgery planning, as it permits adjustment of the breast resection volume.
Keyphrases
- minimally invasive
- coronary artery bypass
- magnetic resonance imaging
- epidermal growth factor receptor
- surgical site infection
- ejection fraction
- endothelial cells
- poor prognosis
- lymph node
- tyrosine kinase
- radiation therapy
- magnetic resonance
- stem cells
- neoadjuvant chemotherapy
- computed tomography
- mesenchymal stem cells
- sentinel lymph node
- adipose tissue
- end stage renal disease
- healthcare
- coronary artery disease
- advanced non small cell lung cancer
- skeletal muscle