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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.
This Phase III Trial evaluates whether breast conservation surgery and endocrine therapy results in a non-inferior rate of invasive or non-invasive ipsilateral breast tumor recurrence (IBTR) compared to breast conservation with breast radiation and endocrine therapy.
The goal of this phase I clinical trial is to evaluate the usefulness of an imaging test (zirconium Zr89 panitumumab \[89Zr panitumumab\]) with positron emission tomography (PET)/computed tomography (CT) for diagnosing the spread of disease from where it first started (primary site) to other places in the body (metastasis) in patients with head and neck squamous cell carcinoma. Traditional PET/CT has a low positive predictive value for diagnosing metastatic disease in head and neck cancer. 89Zr panitumumab is an investigational imaging agent that contains radiolabeled anti-EGFR antibody which is overexpressed in head and neck cancer. The main question this study aims to answer is the sensitivity and specificity of 89Zr panitumumab for the detection of indeterminate metastatic lesions in head and neck cancer. Participants will receive 89Zr panitumumab infusion and undergo 89Zr panitumumab PET/CT 1 to 5 days after infusion. Participants will otherwise receive standard of care evaluation and treatment for their indeterminate lesions. Researchers will compare the 89Zr panitumumab to standard of care imaging modalities (magnetic resonance imaging (MRI), CT, and/or PET/CT).
The purpose of this study is to determine if panitumumab-IRDye800 is effective in identifying cancer, compared to surrounding normal tissue, and the further characterize the safety profile of this drug.
This is an open-label, multicenter, two-arm Phase II clinical trial that will evaluate the impact of 2nd line chemotherapy (i.e. capecitabine) on survival in patients with non-Luminal A hormone receptor-positive (HR+) metastatic breast cancer (MBC)

About SHE in Oncology

  • Huntsman Cancer Institute
  • Massey Cancer Center
  • Case Comprehensive Cancer Center
  • The James (The Ohio State University Comprehensive Cancer Center)
  • Vanderbilt-Ingram Cancer Center
  • Virtual, hands-on cancer research experience with laboratory kit sent to your home
  • Targeted career development and skill-building workshops with professionals from diverse sectors of cancer research and care
  • Network of peers and mentors across program sites
  • $500 stipend for participation
  • Must be a rising high school sophomore, junior, or senior who identifies as female within the VICC catchment area
  • Must commit to 4 hours of virtual meetings Monday through Friday for two weeks in the summer during the specified dates
  • Students who are interested in scientific investigation and eager to learn will benefit most from the program.

2025 program dates are July 7 - July 18, 2025.

The deadline for applications is April 3, 2025 by 11:59 pm (CDT). VICC will accept 30 students from within our catchment area for the 2025 program. Interested students are asked to complete an application that includes a statement of interest and a recommendation letter from a science teacher. The 2025 application will be available soon and can be found here once available.

For more information, please email SHE@vumc.org.

Click here to view an informational sheet for teachers

About the VERTICAL Program

Leveraging the strengths of the Vanderbilt-Ingram Cancer Center, Vanderbilt University, and Vanderbilt University Medical Center, this paid program will immerse you in a research laboratory for 2 years working with a Vanderbilt faculty member on a cutting-edge cancer research project.

Participants will receive a stipend and benefits. Through this program you will gain the knowledge, skills, and community to further your career in cancer research or medicine.

In addition to your research, fellows will participate in:

  • Responsible Conduct in Research training
  • Interdisciplinary Graduate Program (IGP) coursework
  • Individualized research development plan
  • Introduction to Cancer Biology course
  • Clinical Cancer Medicine course
  • GRE or MCAT preparatory course
  • Meharry Medical College (MMC)-Vanderbilt-Tennessee State University (TSU) Cancer Partnership (MVTCP) online modules
  • Cancer Biology Science Hour presentation
  • VICC Annual Scientific Retreat, MVTCP retreat, and other retreats
  • Scientific conferences
  • Career Path Lunch & Learn Sessions
  • Online resources from Vanderbilt University, Nature Masterclass
  • Science & Community Impact Talks
  • Volunteer opportunities

 

Eligible candidates for the VERTICAL program will be:

  • Individuals with bachelor’s degrees from nationally accredited colleges or universities who desire to pursue doctoral degrees and careers in science or medicine, with a focus on cancer.
  • Able to commit to the full-time, 2-year program which runs from August 2025 – August 2027 in Nashville, Tennessee.
  • Individuals who are interested in pursuing doctoral degrees and careers in science or medicine, with a focus on cancer, will benefit most from the program.

For those interested in applying for the 2025-2027 VERTICAL Program, please complete an interest form here 
The formal application will be available in January and sent to those who have completed the interest form. Please see below for the list of required application components.

  • One-page statement of interest
  • Copy of college transcript (does not need to be official)
  • Two letters of recommendation from prior educators and/or employers
  • A current resume or CV

All program questions should be directed to VERTICAL@vumc.org.

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