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Breast Cancer: Diagnosis, Treatment, and Advancements
An overview of breast cancer diagnosis, treatment, and the latest advancements in personalized medicine.
Spanish
Spain
HealthGender IssuesCancerTreatmentGeneticsDiagnosisBreast Cancer
Sociedad Española De Oncología Médica (Seom)Hospital Universitario De SalamancaComisión EuropeaSistema Nacional De Salud
César A. Rodríguez
- What are the major challenges and goals in breast cancer treatment?
- Improving breast cancer outcomes involves multidisciplinary treatment teams and comprehensive care for long-term survivors, addressing physical and emotional effects. The goal is to improve survival rates while minimizing treatment side effects and ensuring a high quality of life.
- What are the different types of breast cancer and how are they classified?
- Breast cancer is classified into luminal, HER2-positive, and triple-negative subtypes based on molecular characteristics, influencing treatment decisions. Luminal tumors depend on hormones, HER2-positive tumors have high HER2 protein levels, and triple-negative tumors lack both hormone and HER2 receptors.
- What advanced diagnostic techniques are used to personalize breast cancer treatment?
- Advanced diagnostic techniques like liquid biopsy and massive sequencing enable personalized treatment. Liquid biopsy analyzes circulating tumor DNA to identify genomic changes for tailored treatment; massive sequencing analyzes numerous mutations for optimal therapy.
- When should a woman get a mammogram, and what is the role of self-breast examination?
- Mammography is recommended for women aged 45-74, every two years, to detect breast cancer early. While self-examination can't replace mammography, it helps identify alarming signs like lumps, redness, or nipple discharge, prompting medical consultation.
- What is the significance of family history in breast cancer, and how does genetic testing work?
- A family history of breast cancer, especially BRCA1 or BRCA2 mutations, increases the risk, particularly in younger women. Genetic testing is not universal; genetic counseling assesses risk and determines the need for blood testing to identify these mutations.