Using Biopsies to Inform Response Characteristics in Kidney Cancer

Commentary
Video

Observing changes in the tumor microenvironment before and after a biopsy may elucidate how kidney cancer cells interact with immune cells.

As part of a collaboration with KidneyCAN, CancerNetwork® spoke with Eric Jonasch, MD, regarding biopsy-driven research organized by the Kidney Cancer Research Consortium to better understand how patients with kidney cancer respond to therapy.

Jonasch, a professor in the Department of Genitourinary Medical Oncology of the Division of Cancer Medicine and the director of the von Hippel Lindau Center at The University of Texas MD Anderson Cancer Center, described a process of collecting biopsies during a patient’s treatment course for kidney cancer. By observing differences in the tumor microenvironment before and after biopsy collection, it may be possible to determine whether patients require new types of treatment for their disease.

KidneyCAN is a nonprofit organization with a mission to accelerate cures for kidney cancer through education, advocacy, and research funding. Learn more about KidneyCAN’s mission and work here.

Transcript:

[For] most of the clinical trials that we are launching, we’re trying to incorporate the use of biopsies, mainly on treatment. We will have, at baseline, some biopsies as well that will have been acquired in the course of the patient’s care. We want to look at how the tumor microenvironment changes as a function of the therapy we’re giving. You have a pre-biopsy [and] a post-biopsy; how does it change? By looking at these changes, we’re going to be able to understand—in those individuals who are responding—what the characteristics of the cancer cells interacting with the immune cells. Conversely, in individuals who aren’t responding, how does that microenvironment look? By looking at what’s good and what’s not good with regard to a response at a tissue level, we can then generate hypotheses. “Well, here’s why the response isn’t occurring.”

There might be something here. By understanding that, we can then postulate that new types of treatments might be needed for those individuals. That’s what we’re trying to do. Having what I would call a data-rich and knowledge-rich set of trials allows us to make multiple observations within a smaller data set of patients, which is more efficient. It’s better for patients; fewer patients have to be tested, and we gain knowledge faster.

Recent Videos
Data from the phase 3 DeLLphi-304 trial at ASCO 2025 revealed a survival advantage with tarlatamab vs chemotherapy in second-line ES-SCLC.
The new peritoneal surface malignancy care guidelines had clinicians gather from every disease state to show increased representation.
The FDA approval of tarlatamab in SCLC has received much press attention, according to Daniel R. Carrizosa, MD, MS.
These new guidelines aim to alleviate some of the problems caused by patients with peritoneal metastases being diagnosed with the disease in late stages.
A combined cohort composed of patients from the TROPION-Lung01 and TROPION-Lung-05 trials showed a survival advantage with dato-DXd vs docetaxel.
The National ICE-T Conference may inspire future collaboration between community and academic oncologists in the management of different cancers.
Osimertinib/chemotherapy and amivantamab/lazertinib have exhibited an efficacy advantage vs osimertinib in patients with EGFR-mutant NSCLC.
One of the largest obstacles to tackle in the kidney cancer landscape will be translating the research on rare kidney cancer subtypes into clinical trials.
Long-term toxicities like infections and secondary primary malignancies remain a concern when sequencing novel agents for those with multiple myeloma.
Related Content