NIH-funded research R37 grant

Understanding how certain kidney cancers worsen with immunotherapy

Official title: Mechanisms of Hyperprogression to Immunotherapy in SMARCB1-Deficient Renal Malignancies

Funded at University of Tx Md Anderson Can Ctr · NIH-11047703 · Data updated 2026-11-12

This study is looking at why certain kidney cancers, especially in young people of African descent, get worse quickly when treated with immunotherapy, and it aims to find better treatments by understanding the unique features of these tumors.

Quick facts

Grant typeR37 grant
Study typeNIH-funded research
Funding institutionUniversity of Tx Md Anderson Can Ctr
NIH-funded
Lab location1 site (Houston, United States)
Project startApril 1, 2024
Project endMarch 31, 2029
Funding year2025
Award (this year)$672,300
NIH project number5R37CA288448-02
Project IDNIH-11047703 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research are young individuals of African descent diagnosed with SMARCB1-deficient renal malignancies, particularly those with renal medullary carcinoma.

Less likely to help

Patients with renal malignancies that do not involve SMARCB1 deficiency or those who do not fit the demographic profile may not benefit from this research.

What this research studies

This research investigates the mechanisms behind the rapid worsening of SMARCB1-deficient renal malignancies, particularly renal medullary carcinoma, when treated with immunotherapy. It focuses on how these tumors, which are more common in young individuals of African descent, respond poorly to standard treatments due to their unique biological characteristics. The study aims to identify specific genetic and molecular pathways that lead to this hyperprogression, with the goal of developing targeted therapies that could improve patient outcomes. By analyzing tissue samples and using advanced mouse models, researchers hope to uncover new strategies to counteract this aggressive cancer behavior.

Why it matters

Potential benefit: If successful, this research could lead to more effective treatment options for patients with SMARCB1-deficient renal malignancies, potentially improving survival rates.

How similar studies have gone: While the specific mechanisms of hyperprogression in SMARCB1-deficient tumors are being explored, similar research has shown promise in understanding immune responses in other aggressive cancers, indicating potential for success.

Where this research is happening

  • University of Tx Md Anderson Can Ctr
    Houston, United States
    Active

Researchers

  • Principal investigator: Msaouel, Pavlos — University of Tx Md Anderson Can Ctr
  • Study coordinator: Msaouel, Pavlos

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.