Treat breast cancer patients sooner
Rapid test yields results in 10–14 days
When it comes to breast cancer treatment, recent studies have shown that a longer time to treatment completion has a negative impact on the overall outcome and survival of patients.1,2
Mayo Clinic Laboratories’ Rapid Breast Cancer Treatment Decision Panel (Mayo ID: BRTP) is designed to detect 11 genes that are linked to lifetime breast cancer risk, in alignment with guidelines established by the National Comprehensive Cancer Network (NCCN). With results delivered in 10–14 days, clinicians and patients will have the information they need to quickly guide treatment decisions.
Breast cancer panel halves turnaround time
In this test-specific episode of the "Answers From the Lab" podcast, Wei Shen, Ph.D., explains how Mayo Clinic Laboratories' new breast cancer panel provides rapid results to guide critical decisions about treatment and screening.
Diagnosis and treatment options
Of the 11 genes our rapid breast cancer panel is designed to detect, seven are considered high risk based on National Comprehensive Cancer Network (NCCN) guidelines for breast cancer risk management and treatment.
The high-risk genes (BRCA1, BRCA2, CDH1, PALB2, PTEN, STK11, and TP53) carry a 40%–60% lifetime likelihood of the presence of cancer. NCCN guidelines also include recommendations regarding prophylactic surgeries for the seven high-risk genes. If any of the seven high-risk genes are detected, NCCN guidelines recommend starting mammograms or breast MRIs at a much younger age (potentially as young as 20 years old, depending on which gene is involved).
Our panel also includes four moderate-risk genes, allowing clinicians to cast a broader net and reduce the need for subsequent reflex testing. The four moderate-risk genes (ATM, CHEK2, RAD51C, and RAD51D) indicate a 20%–40% lifetime likelihood of cancer occurrence.