PD-L1 Biomarker for Immunotherapy

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.

What is ER-Low Breast Cancer?

Pathology examination 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.

What Do My Test Results Mean?
What Do Current Guidelines Say?
Should ER Low Breast Cancers Be Treated With Hormonal Therapy?
What Are The Treatment Options for ER-Low Breast Cancer?
  • TNBC Clinical Trials For ER-Low Breast Cancer Breast cancers that have any number of estrogen receptors, including those defined as ER-low, are currently treated with hormonal therapies. But some clinical trials for triple negative breast cancer (TNBC) accept people with ER-low cancers. See trials on Metastatic Trial Search that are accepting participants who qualify as ER-low.
  • Clinical Trials for ER Positive Breast Cancer People with ER-low breast cancer may also qualify for clinical trials for estrogen positive (ER+) breast cancer. See clinical trials for estrogen positive breast cancer on Metastatic Trial Search.

HER2 Positive Metastatic Breast Cancer Research Update

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.

What Does HER2 Positive Mean?
  • Breast Cancer HER2 Status  The American Cancer Society describes, in simple terms, what HER2 positive means and what test doctors use to determine whether a tumor is HER2 positive or HER2 negative.
How HER2 Positive is Typically Treated 
What’s New in HER2 Positive MBC
What’s in the Pipeline?
  • Emerging Areas in Metastatic Breast Cancer Treatment  Susan G. Komen breaks down treatments on the rise and under study for metastatic breast cancer. For HER2 positive disease, the most helpful sections are HER2 Targeted Therapies, HER2 antibody drug conjugates, and Tyrosine kinase inhibitors.
  • Clinical Trials for HER2 Positive MBC Metastatic Trial Search provides a list of over 100 clinical trials for people with HER2 positive metastatic breast cancer.

See all articles on this site tagged with HER2 Positive breast cancer

Recent FDA Approvals for Metastatic 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.

Tucatinib (Tukysa®)
Sacituzumab govetican (Trodelvy®)
Trastuzumab deruxtican (Enhertu®)
Relevant Topics on Metastatic Trial Talk (MTT)

The Tumor Microenvironment

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.

Tumor microenvironment
Tumor microenvironment and MBC
Tumor microenvironment related clinical trials

What is Your Tumor’s Mutation Burden?

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.

Triple-Negative Breast Cancer Update

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.