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Ryan Merrell, MD

  • Associate Professor of Clinical Neurology

Ryan Merrell, MD

  • Associate Professor of Clinical Neurology

ryan.merrell@vumc.org

Research Program

Research Description

Have any questions? Contact Us 1-877-936-8422 for more information

Douglas Kojetin, PhD

  • Co-Leader, Genome Maintenance Research Program
  • Ingram Professor of Cancer Research
  • Professor of Biochemistry

Email

douglas.kojetin@Vanderbilt.Edu
2200 Pierce Avenue, 842/846 RRB
Nashville, TN 37232

Douglas Kojetin, PhD

  • Co-Leader, Genome Maintenance Research Program
  • Ingram Professor of Cancer Research
  • Professor of Biochemistry

douglas.kojetin@Vanderbilt.Edu

2200 Pierce Avenue, 842/846 RRB
Nashville, TN 37232

Research Program

Research Description

Have any questions? Contact Us 1-877-936-8422 for more information

Gary Smith, MD

  • Professor of Radiology and Radiological Sciences
  • Chief, Nuclear Medicine and PET/CT, Nashville Veterans Administration Medical Center

Email

gary.t.smith@vumc.org
1161 21st Avenue South
Nashville, TN 37232

Gary Smith, MD

  • Professor of Radiology and Radiological Sciences
  • Chief, Nuclear Medicine and PET/CT, Nashville Veterans Administration Medical Center

gary.t.smith@vumc.org

1161 21st Avenue South
Nashville, TN 37232

Research Program

Have any questions? Contact Us 1-877-936-8422 for more information

Marcus Dillender, Ph.D.

  • Assistant Professor of Economics
  • Assistant Professor of Medicine, Health, and Society

Marcus Dillender, Ph.D.

  • Assistant Professor of Economics
  • Assistant Professor of Medicine, Health, and Society

marcus.o.dillender@Vanderbilt.Edu

Research Program

Have any questions? Contact Us 1-877-936-8422 for more information
The investigational drug to be studied in this protocol, BCA101, is a first-in-class compound that targets both EGFR with TGF. Based on preclinical data, this bifunctional antibody may exert synergistic activity in patients with EGFR-driven tumors.
This phase II trial compares the effect of usual treatment of docetaxel chemotherapy plus trastuzumab, to ado-emtansine (T-DM1) in patients with HER2-postive salivary gland cancer that has come back (recurrent), that has spread from where it first started (primary site) to other places in the body, or cannot be removed by surgery (unresectable). This trial is also testing how well trastuzumab deruxtecan works in treating patients with HER2-low recurrent or metastatic salivary gland cancer. Trastuzumab is a form of targeted therapy because it works by attaching itself to specific molecules (receptors) on the surface of cancer cells, known as HER2 receptors. When trastuzumab attaches to HER2 receptors, the signals that tell the cells to grow are blocked and the cancer cell may be marked for destruction by body's immune system. Trastuzumab emtansine contains trastuzumab, linked to a chemotherapy drug called emtansine. Trastuzumab attaches to HER2 positive cancer cells in a targeted way and delivers emtansine to kill them. Trastuzumab deruxtecan is a monoclonal antibody called traztuzumab, linked to a chemotherapy drug called deruxtecan. Trastuzumab is a form of targeted therapy because it attaches to specific molecules (receptors) on the surface of cancer cells, known as HER2 receptors and delivers deruxtecan to kill them. Docetaxel is in a class of medications called taxanes. It stops cancer cells from growing and dividing and may kill them. Trastuzumab emtansine may work better compared to usual treatment of chemotherapy with docetaxel and trastuzumab or trastuzumab deruxtecan in treating patients with recurrent, metastatic or unresectable salivary gland cancer.
This phase II trial tests how well pB1-11 and human papillomavirus tumor antigen (TA-HPV) vaccines in combination with pembrolizumab work in treating patients with oropharyngeal cancer that has come back (recurrent) or that has spread from where it first started (primary site) to other places in the body (metastatic) and that is PD-L1 and human papillomavirus (HPV) positive. Oropharyngeal cancer is a type of head and neck cancer involving structures in the back of the throat (the oropharynx), such as the non-bony back roof of the mouth (soft palate), sides and back wall of the throat, tonsils, and back third of the tongue. Scientists have found that some strains or types of a virus called HPV can cause oropharyngeal cancer. pBI-11 is a circular deoxyribonucleic acid (DNA) (plasmid) vaccine that promotes antibody, cytotoxic T cell, and protective immune responses. TA-HPV is an investigational recombinant vaccina virus derived from a strain of the vaccina virus which was widely used for smallpox vaccination. Vaccination with this TA-HPV vaccine may stimulate the immune system to mount a cytotoxic T cell response against tumor cells positive for HPV, resulting in decreased tumor growth. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread by inhibiting the PD-1 receptor. These investigational vaccines could cause or enhance an immune response in the body against HPV, during which time the activity of pembrolizumab against oropharyngeal cancer associated with HPV may be strengthened. These drugs in combination may be more effective in increasing the ability of the immune system to fight oropharyngeal cancer than pembrolizumab alone.
This research is to evaluate the effectiveness of Talazoparib as a potential treatment for metastatic breast cancer with a BRCA 1 or BRCA 2 mutation.
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