A Vaccine (STEMVAC) With Standard Endocrine-Based Therapy or Chemotherapy for the Treatment of Metastatic Hormone Receptor Positive, HER2 Negative Breast Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Washington

About this trial

This phase II trial studies how well a vaccine, STEMVAC, works in combination with standard endocrine-based therapy (ET) with a CDK4/6 targeted drug therapy, or with the chemotherapy drug capecitabine, in treating patients with hormone receptor (HR)-positive, HER2-negative breast cancer that has spread from where it first started (primary site) to other places in the body (metastatic). STEMVAC is designed to target proteins that cancer cells use when they become more aggressive and start to spread, and it is believed to work by boosting the immune system to recognize and destroy the invader tumor cells that are causing the disease. Standard ET is treatment that adds, blocks, or removes hormones in order to slow or stop the growth of cancer. Standard CDK4/6 inhibitors, including abemaciclib, may stop the growth of tumor cells and may kill them by blocking some of the enzymes needed for cell growth. Capecitabine is in a class of medications called antimetabolites. It is taken up by tumor cells and breaks down into fluorouracil, a substance that kills tumor cells. Giving STEMVAC in combination with standard ET or chemotherapy may be an effective treatment for metastatic HR positive, HER2 negative breast cancer.

Eligibility criteria

Qualifiers

Patients must be at least ≥ 18 years of age

Histologically confirmed hormone receptor positive metastatic breast cancer: Tumors that are positive for estrogen receptor (ER) and/or progesterone receptor (PR)

0-1+ HER2 expression by immunohistochemistry (IHC) OR

Fluorescence in situ hybridization (FISH) negative OR

Disqualifiers

Symptomatic restrictive cardiomyopathy

Dilated cardiomyopathy

Unstable angina within 4 months prior to enrollment

New York Heart Association functional class III-IV heart failure on active treatment

Trial design

Treatments tested in this trial

  • CD105/Yb-1/SOX2/CDH3/MDM2-polyepitope Plasmid DNA Vaccine
  • Capecitabine
  • Computed Tomography
  • Cyclin-Dependent Kinase 4 Inhibitor
  • Cyclin-Dependent Kinase 6 Inhibitor
  • F-18 16 Alpha-Fluoroestradiol
  • Hormone Therapy
  • Positron Emission Tomography
  • Biopsy Procedure
  • Biospecimen Collection
  • Abemaciclib

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators