Among patients with hormone receptor (HR)-positive, HER2-negative, low-risk ductal carcinoma in situ (DCIS), those who underwent active monitoring had similar two-year invasive ipsilateral breast cancer recurrence rates as those who underwent guideline-concordant treatment, according to results from the COMET clinical trial presented at the San Antonio Breast Cancer Symposium (SABCS), held December 10-13, 2024.
Bristol Myers Squibb gets FDA approval to begin production
A research campus operated by Bristol-Myers Squibb in Lawrenceville, New Jersey. Credit: Coolcaesar/ commons.wikimedia.org. The US Food and Drug Administration (FDA) has granted approval to
June 9, 2023