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January 23, 2026Cancer Research0 citations

Abstract IA003: Advances in using germline genetics to inform prostate cancer risk assessment and disease progression

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BDBurcu F. Darst

Key Result

The polygenic risk score (PRS) effectively predicts prostate cancer risk and progression, enhancing screening strategies for diverse populations.

Key Points

  • The research aims to enhance prostate cancer risk assessment and inform screening practices through genetics.
  • Identified strong genetic risk factors for prostate cancer.
  • Developed a polygenic risk score to predict prostate cancer risk.
  • Conducted a multi-ancestry genome-wide association study focused on prostate cancer aggressiveness.
  • Evaluated the predictive capability of the PRS for disease progression in low-risk patients.
  • Noted a 6% annual increase in distant prostate cancer diagnoses.
  • Established that the PRS is predictive of upgrading risk in patients on active surveillance.
  • Enhanced the PRS to better differentiate between aggressive and indolent prostate cancer.
  • Anticipated identification of new genetic mechanisms contributing to aggressive forms of prostate cancer.

Structured PICO

Does a polygenic risk score predict prostate cancer risk and disease progression in patients on active surveillance?

P
Population
Patients at risk for prostate cancer and patients diagnosed with low-risk prostate cancer being monitored on active surveillance
I
Intervention
Polygenic risk score (PRS) based on germline genetics
O
Outcome
Prostate cancer risk and risk of upgrading or extreme upgrading (to grade group 3 or higher) during active surveillance

Polygenic risk scores based on germline genetics can help stratify prostate cancer risk and predict disease progression, potentially informing screening and treatment decisions.

Abstract

Abstract The decline in prostate cancer screening in recent years has led to a 6% annual increase in patients diagnosed with distant prostate cancer, where the 5-year survival rate is only 38%, demonstrating the urgent need to improve prostate cancer screening practices. Prostate cancer is highly heritable and presents a unique opportunity to implement risk-stratified screening. Accordingly, we have identified many strong genetic risk factors of prostate cancer and developed a polygenic risk score (PRS) that is highly predictive of prostate cancer risk across diverse populations, which could inform the decision to initiate screening, along with the optimal age and frequency of screening. Several of these genetic factors have implications beyond screening—for instance, among patients diagnosed with low-risk prostate cancer being monitored on active surveillance, the PRS was predictive of risk of upgrading or extreme upgrading (i. e. , to grade group 3 or higher) along with a higher percentage of cancerous biopsy cores. In recent work, we demonstrated that it is possible to improve the ability of the PRS to distinguish risk of advanced from indolent prostate cancer. This has launched an effort to characterize the common genetic architecture of aggressive prostate cancer by undertaking a large-scale multi-ancestry genome-wide association study (GWAS) focused on prostate cancer aggressiveness. This work is anticipated to identify new genetic mechanisms contributing to the etiology of lethal prostate cancer while also advancing PRS and clinical models to inform prostate cancer screening and treatment decisions. Citation Format: Burcu F. Darst. Advances in using germline genetics to inform prostate cancer risk assessment and disease progression abstract. In: Proceedings of the AACR Special Conference in Cancer Research: Innovations in Prostate Cancer Research and Treatment; 2026 Jan 20-22; Philadelphia PA. Philadelphia (PA): AACR; Cancer Res 2026;86 (2Suppl): Abstract nr IA003.

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Cite This Study

Burcu F. Darst (2026) studied this question. The polygenic risk score (PRS) effectively predicts prostate cancer risk and progression, enhancing screening strategies for diverse populations.

synapsesocial.com/papers/69730fe2c8125b09b0d1f946https://doi.org/10.1158/1538-7445.prostateca26-ia003
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