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Claudia Gonzalez-Hunt, Ph.D.

  • Assistant Professor of Medicine (Genetic Medicine)

Claudia Gonzalez-Hunt, Ph.D.

  • Assistant Professor of Medicine (Genetic Medicine)

claudia.gonzalezhunt@vumc.org

Research Program

Research Description

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

Brian Shirts, M.D., Ph.D.

  • Associate Professor of Pathology, Microbiology and Immunology

Brian Shirts, M.D., Ph.D.

  • Associate Professor of Pathology, Microbiology and Immunology

b.shirts@vumc.org

Research Program

Research Description

Have any questions? Contact Us 1-877-936-8422 for more information
This phase I/II trial studies the side effects and best dose of M3814 and to see how well it works when given together with radiation therapy in treating patients with pancreatic cancer that cannot be removed by surgery and has not spread to other parts of the body (localized). M3814 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Hypofractionated radiation therapy delivers higher doses of radiation therapy over a shorter period of time and may kill more tumor cells and have fewer side effects. Giving M3814 and hypofractionated radiation therapy together may work better than radiation therapy alone in the treatment of patients with localized pancreatic cancer.

AI researchers develop new technologies for cancer care  

Submitted by vicc_news on

Researchers at Vanderbilt University Medical Center using artificial intelligence have helped develop two technologies for improving cancer care. 

One technology called MSI-SEER, described in a study published in npj Digital Medicine, better predicts microsatellite instability-high status from standard pathology slides and provides clinicians with specific data, including any uncertainties with predictions. The other technology, a breakthrough three-dimensional imaging tool described in a study published in Nature Communications, has transformative potential beyond cancer diagnostics. 

These new technologies showcase how VUMC researchers are using the power of AI to meet a wide range of medical needs, said Tae Hyun Hwang, PhD, professor of Surgery, founding director of the Molecular AI Initiative, and director of AI Research for the Vanderbilt Section of Surgical Sciences. He noted that the 3D imaging could significantly advance development of therapeutic drugs, provide more detailed assessments of organ transplant rejections, assist with personalized medicine, and aid with tissue analysis for biopharmaceutical development. 

Tae Hyun Hwang, PhD
Tae Hyun Hwang, PhD

“This technology fundamentally redefines how we visualize and analyze tissue architecture, moving from traditional two-dimensional views to full 3D microenvironment mapping at the subcellular level,” said Hwang, a corresponding author of the study, who provided senior leadership in the development, validation and translational development of the technology. 

The 3D study published in Nature Communications introduced an innovative framework that integrates holotomography with deep learning to generate hematoxylin- and eosin-stained images directly from thick tissue samples. This noninvasive, AI-driven approach preserves tissue integrity, overcomes the traditional 4- to 5-micron thickness limit of routine histology, and enables volumetric visualization of biological structures up to 50 microns thick. 

By preserving tissue samples and avoiding chemical alteration, this method also ensures compatibility with downstream molecular assays, such as spatial transcriptomics, proteomics and genomic profiling — enhancing the breadth and depth of diagnostic and research capabilities.  

“This is not just a digital copy of hematoxylin- and eosin-staining,” Hwang said. “It is a foundational platform for AI-driven volumetric tissue analysis that accelerates discoveries in oncology, immunology, regenerative medicine and therapeutic development.” 

The multi-institutional effort also included researchers from KAIST, Tomocube Inc., Yonsei University College of Medicine and Mayo Clinic. Hwang received funding support from the National Cancer Institute (grants R01CA276690, R37CA265967, U01CA294518). 

VUMC researchers developed the MSI-SEER predictor technology in collaboration with Mayo Clinic, Yonsei Severance Hospital and Seoul St. Mary’s Hospital in South Korea. This technology identifies patients who will benefit from an immunotherapy that might otherwise be missed with existing prediction models. 

Microsatellite instability-high (MSI-H) status is a well-established biomarker used to identify patients likely to respond to immune checkpoint inhibitors, especially patients with gastrointestinal cancers. However, traditional testing methods — including immunohistochemistry and PCR-based assays — offer only a binary result and often miss focal or heterogeneous MSI-H regions within tumors.  

MSI-SEER overcomes this limitation by dividing each pathology slide into thousands of image tiles and generating region-by-region predictions of MSI-H probability. This enables visualization of the tumor’s spatial heterogeneity and quantification of the MSI-H fraction across the tumor. In multiple cases, MSI-SEER identified MSI-H regions in tumors previously classified as microsatellite stability, and those patients subsequently responded to immunotherapy. 

“This is analogous to what we say in HER2-low gastric cancer, where patients previously not eligible for targeted therapy are now being treated with agents like trastuzumab deruxtecan,” Hwang said. “Likewise, patients with low or heterogeneous MSI-features may now be reconsidered for immunotherapy if spatially resolved analysis like MSI-SEER is used.” 

A key innovation of MSI-SEER is its ability to report not only predictions but the confidence level for each result.  

“AI should not dictate clinical decisions; it should support them,” Hwang said. “MSI-SEER gives clinicians both the answer and a measure of how reliable the answer is. It’s not about replacing human expertise but about combining the best of AI computation with physician judgment to drive safe, precise decisions.” 

Hwang, who conceptualized the study and is the paper’s senior author, received research support from the National Cancer Institute and the Department of Defense. He also received support from the Eric and Wendy Schmidt Fund for AI Research and Innovation and the American Association for Cancer Research Innovation and Discovery Grant.  

Other VUMC researchers who authored the study are Sunho Park, PhD, Minji Kim, MS, Jean Clemenceau, PhD, and Inyeop Jang, PhD. 

The post AI researchers develop new technologies for cancer care   appeared first on VUMC News.

Andreana Holowatyj named ‘40 Under 40 In Cancer’ winner

Submitted by vicc_news on
Andreana Holowatyj, PhD, MSCI

Andreana Holowatyj, PhD, MSCI, assistant professor of Medicine, has been named to the 40 Under 40 In Cancer Class of 2025 by the Association for Value-Based Cancer Care.

This year’s class was selected from more than 3,000 nominations. The awards initiative identifies and recognizes contributions across the field of cancer by rising stars and emerging leaders under the age of 40. 

Holowatyj’s research is focused on early-onset cancers, including colorectal and appendiceal cancers. She has received the National Cancer Institute’s Method to Extend Research in Time (MERIT) Award to support her ongoing investigation into how early-onset colorectal cancer and its treatments impact reproductive health. MERIT Awards provide longer-term funding than is typical for most grants to early-stage investigators whose research competence and productivity are distinctly superior and who are highly likely to continue to perform in an outstanding manner. As part of this Award, Holowatyj established and leads the Preserving Fertility After Colorectal Cancer (PREFACE) clinical study, which is currently recruiting patients.  

She is focused on providing evidence-based guidance that will ultimately improve clinical care and outcomes for individuals ages 18 to 49 when diagnosed with cancer. Holowatyj and her team discovered that 1 in 2 young cancer patients report that a health care provider involved in their cancer care did not discuss options to preserve fertility prior to starting cancer treatment. 

Her research has been published in high-impact medical research journals and has led to clinical practice changes and revisions to consensus guidelines. She has also been invited to serve on several international committees, including the American Joint Committee on Cancer Lower Gastrointestinal Tract Expert Panel that updates clinical cancer staging systems, the Fight Colorectal Cancer Global Early-Onset Colorectal Cancer Think Tank, and as the inaugural chair of the Scientific Advisory Board for the Appendix Cancer Pseudomyxoma Peritonei (ACPMP) Research Foundation. This year, with the support of the ACPMP Research Foundation, she led an expert recommendation report in the journal Nature Reviews Cancer that identified six key research priority areas to deliver a fundamental understanding of appendiceal tumors and to improve treatments and outcomes for patients with this rare cancer.

The post Andreana Holowatyj named ‘40 Under 40 In Cancer’ winner appeared first on VUMC News.

This is a Phase 1/2, open-label, multicenter, study of the safety, tolerability, PK, PD, and anti-tumor activity of MRTX1719 patients with advanced, unresectable or metastatic solid tumor malignancy with homozygous deletion of the MTAP gene.
This open-label research study is studying (Z)-endoxifen as a possible treatment for pre-menopausal (still having periods) women with ER+/HER2- breast cancer. (Z)-endoxifen is a selective estrogen receptor modulator or "SERM." SERMs work to treat cancer by blocking the body's natural estrogen from binding to cancer cells. This study includes a pharmacokinetic part (PK, how the drug works in your body) and a treatment part. The primary purpose of the study is to see how (Z)-endoxifen works on tumor cell growth by monitoring a cancer marker called Ki-67. Ki-67 will be measured by biopsy of the breast after about 4 weeks of treatment. If your cancer is responding to treatment based on the Ki-67 results, you may continue treatment up to 24 weeks or until surgery. The PK part of the study will be enrolled first, enrolling about 18 study participants who will all receive oral once daily (Z)-endoxifen treatment. 12 of these participants will be randomly assigned to treatment with an equal (50/50) chance to be assigned to (Z)-endoxifen or (Z)-endoxifen + goserelin (a medication given to block the ovaries from making estrogen and is also called ovarian suppression). This part of the study will help select the dose of (Z)-endoxifen to use in the treatment part by measuring the levels of (Z)-endoxifen in the blood stream and determine how long it takes for the body to remove it. About 160 study participants will be enrolled in the treatment part. The treatment part will help to determine how oral once daily (Z)-endoxifen, when taken by itself, compares to oral once daily exemestane (a medication that decreases the amount of estrogen in the body, also known as an aromatase inhibitor) and monthly injections of goserelin. Exemestane and goserelin taken together is a standard treatment regimen for premenopausal patients with ER+/HER2- breast cancer. Study participants are randomly assigned to treatment with an equal (50/50) chance to be assigned to (Z)-endoxifen or standard treatment. Study participation is up to 24 weeks of treatment followed by surgery.
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