NIH-funded research R01 grant

Understanding how genetic background affects rare tumors and their treatment responses

Official title: Evaluating the impact of genetic ancestry on the biology and drug response profile of pheochromocytoma and paraganglioma-derived organoid models

Funded at University of Texas Hlth Science Center · NIH-10922102 · Data updated 2026-11-12

This study is looking at how your genetic background might affect the way rare tumors called pheochromocytomas and paragangliomas behave and respond to treatment, especially for patients from underrepresented racial and ethnic groups, to help find better ways to detect and treat these tumors.

More Pheochromocytoma research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Texas Hlth Science Center
NIH-funded
Lab location1 site (San Antonio, United States)
Project startSeptember 8, 2021
Project endAugust 31, 2026
Funding year2024
Award (this year)$265,946
NIH project number3R01CA264248-04S2
Project IDNIH-10922102 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research include individuals from underrepresented racial and ethnic backgrounds diagnosed with pheochromocytomas or paragangliomas.

Less likely to help

Patients with common tumors or those not from the targeted racial and ethnic groups may not benefit from this research.

What this research studies

This research investigates the role of genetic ancestry in the biology and treatment responses of rare neuroendocrine tumors called pheochromocytomas and paragangliomas. By creating patient-derived organoid models, the study aims to identify how genetic factors and social determinants influence tumor behavior and drug effectiveness. The research focuses on underrepresented racial and ethnic minority patients, aiming to improve early detection and treatment options for aggressive forms of these tumors. Patients will be recruited to provide samples that will help develop these innovative models.

Why it matters

Potential benefit: If successful, this research could lead to more personalized and effective treatment strategies for patients with rare tumors.

How similar studies have gone: Previous research has shown promise in using patient-derived organoid models to study cancer, indicating potential for success in this novel approach.

Where this research is happening

  • University of Texas Hlth Science Center
    San Antonio, United States
    Active

Researchers

  • Principal investigator: Dahia, Patricia Leal — University of Texas Hlth Science Center
  • Study coordinator: Dahia, Patricia Leal

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.