Lines of Therapy: New Drugs May Change MBC Treatment
Which therapy to use for the first, second or third line of treatment for metastatic breast cancer is now under rigorous research as more new therapies are available for treating MBC.
Which therapy to use for the first, second or third line of treatment for metastatic breast cancer is now under rigorous research as more new therapies are available for treating MBC.
Do you need surgery or radiation to the breast after an MBC diagnosis? See the current research on this important question.
New research shows that stage 4 breast cancer with HER2-low expression can benefit from a new drug. Learn more.
To qualify for Tecentriq®-based immunotherapy, the cancer must test positive for the PD-L1 protein. Learn what researchers have found about PD-L1 and other biomarkers to identify patients suited for immunotherapy.
Did you know that some breast cancers can be defined as estrogen receptor low (ER-low) breast cancer?
When you’re first diagnosed, a pathologist runs a series of lab tests on the cancer cells to see what drives the breast cancer to grow. Estrogen receptor positive (ER positive) breast cancer cells have proteins that respond to signals from estrogen, telling the cells to grow. Your pathology report will tell you whether the cancer is ER positive, and how many cells in the tumor sample had estrogen receptors.
Right now, any breast cancer with at least 1% of tested cells showing estrogen receptors is considered ER positive. But researchers have found that ER positive cancers that have a low number of cells with estrogen receptors may respond differently to treatment. These breast cancers are called ER-low.
To learn more about reading your test results, understanding ER-low, and what current guidelines are for treating estrogen receptor low breast cancer, see below.
The treatment landscape for HER2 positive metastatic breast cancer has been rapidly evolving. Since February, the FDA has approved three new drugs to treat it: neratinib, tucatinib, and trastuzumab deruxtecan. More continue to look promising in clinical trials. Targeted therapies’ drugs that can attach to certain features of cancer cells have created more research avenues and may potentially lead to more treatment options.
To learn more about what it means to be HER2 positive, how the subtype is typically treated, the latest news in research, and what might be coming down the line, check out the information below.
See all articles on this site tagged with HER2 Positive breast cancer
June 2020
Recent FDA Approvals for Metastatic Breast Cancer
For the past two months, Metastatic Trial Talk brought you the latest about cancer and COVID-19. But while the world focused on coping with the pandemic, the Food and Drug Administration kept drug approvals moving. It approved in April two new medicines for metastatic breast cancer: tucatinib (Tukysa®), for HER2-positive disease, and sacituzumab govetican (Trodelvy®), for triple-negative disease.
Below, read about the FDA approval of each new medicine, who might benefit the most, how the treatments are given and what side effects each may cause. In addition, you’ll find information on the approval of a third drug, trastuzumab deruxtican (Enhertu®), announced in late December.
Scientists have discovered that the microenvironment–the cells that surround a tumor–plays a role in both how tumors grow and how they respond to treatment. Researchers also think that certain treatments, like immune checkpoint inhibitors, work in part because of the effect they have on the tumor’s microenvironment.
Below you will find articles and video presentations that discuss the microenvironment, different avenues of tumor microenvironment research scientists are pursuing, and clinical trials listed on BreastCancerTrials.org studying a treatment’s affect on a tumor’s microenvironment.
The term “tumor mutation burden” refers to the number of mutations, or changes, seen in the DNA of your cancer cells. It is now one of the biomarkers used to determine cancer treatments. Studies suggest that tumors with a high number of mutations may be more likely to respond to a type of immunotherapy called a checkpoint inhibitor.
Below you can read more about how researchers are using tumor mutation burden to determine which treatments might be best for which patients. You will also find articles specific to studies that have looked at the relationship between tumor mutation burden and treatment outcomes in patients with metastatic breast cancer.
For women and men with triple-negative breast cancer, chemotherapy has been the primary treatment option. But as scientists learn more about subtypes of triple-negative breast cancer, clinical trials can better match new targeted therapies with specific triple-negative patients. These advances are what led to the FDA approval in March 2019 of the PD-L1 inhibitor atezolizumab (Tecentriq®) to treat women and men with metastatic triple-negative breast cancer whose tumors test positive for PD-L1. And we can expect to see more trials that target specific subtypes of triple-negative cancer in the future.