HMN 2026: How gene variant may affect prostate cancer drug efficacy

Alliance trial reveals gene variant may affect prostate cancer drug efficacy
Single-SNP associations with abiraterone clearance at the SULT2A1 locus, including (A) Locus Zoom plot at SULT2A1 and (B) SuSiE statistical fine-mapping. PIP, posterior inclusion probability. Credit: Clinical and Translational Science (2025). DOI: 10.1111/cts.70425

Data from a major U.S. clinical trial from the Alliance for Clinical Trials in Oncology has uncovered a genetic factor that may inform how to optimize the dosing of abiraterone, a widely used hormone treatment for advanced prostate cancer. Published in Clinical and Translational Science, this secondary analysis of Alliance A032201 could lead to more personalized treatments for patients.

“This study is the first to show how an individual’s genetics can impact how abiraterone is metabolized. These findings could lead to optimized dosing strategies in the future, rather than giving the same dose of the drug to everyone, as we do now,” said author Michael Morris, MD, the Steven A. Greenberg Chair in Prostate Cancer Research at Memorial Sloan Kettering Cancer Center in New York.

The Alliance A031201 trial was a large phase III study conducted by the Alliance, a national research network supported by the National Cancer Institute. The trial enrolled 1,311 men with metastatic castration-resistant prostate cancer and randomized them to enzalutamide, another hormonal therapy, either alone or with abiraterone.

As part of this study, researchers collected genetic data and measured drug levels in the blood to see if certain genes influence how these medications are metabolized. That genomic data was analyzed for this current research.

“We discovered that men who carry a specific version of the gene SULT2A1 clear abiraterone from their bodies more slowly,” said lead author Nadine Norton, Ph.D., Associate Professor of Cancer Biology for the Mayo Clinic in Jacksonville, FL. “This means the drug stays in the system longer, which could affect how well it works and whether side effects occur.”

Interestingly, the study did not find any similar genetic effect for enzalutamide, suggesting that this discovery is unique to abiraterone. This finding opens the door to more personalized care. In the future, doctors may be able to test for this gene variant (found in about 15% of people of European descent) and adjust abiraterone doses to make treatment safer and more effective.

“The initial trial gave us the data to make this discovery,” added Dr. Morris, who was study chair of the original Alliance study. “This new genetic finding is an important step toward precision medicine in prostate cancer care.”

In addition to Drs. Morris and Norton, investigators for this current research included scientists from Dartmouth University, Johns Hopkins University, Memorial Sloan Kettering Cancer Center, The Ohio State University, University of Chicago, University of Maryland, University of Michigan and the National Institutes of Biomedical Innovation in Osaka, Japan.

More information

Nadine Norton et al, Association of SULT2A1 Locus With Abiraterone Clearance in the AllianceA031201: Randomized PhaseIIIStudy of Enzalutamide Compared With Enzalutamide Plus Abiraterone for Metastatic Castration?Resistant Prostate Cancer, Clinical and Translational Science (2025). DOI: 10.1111/cts.70425

Provided by
Alliance for Clinical Trials in Oncology


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