Genomic testing in localized prostate cancer can identify subsets of African-Americans with aggressive disease.
By: Shivanshu Awasthi, G Daniel Grass, Javier Torres-Roca, Peter A S Johnstone, Julio Pow-Sang, Jasreman Dhillon, Jong Park, Robert J Rounbehler, Elai Davicioni, Alex Hakansson, Yang Liu, Angelina K Fink, Amanda DeRenzis, Jordan H Creed, Michael Poch, Roger Li, Brandon Manley, Daniel Fernandez, Arash Naghavi, Kenneth Gage, Grace Lu-Yao, Evangelia Katsoulakis, Ryan J Burri, Andrew Leone, Cesar E Ercole, Joshua D Palmer, Neha Vapiwala, Curtiland Deville, Timothy R Rebbeck, Adam P Dicker, William Kelly, Kosj Yamoah

H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, 33612, USA.
2022-02-21; doi: 10.1093/jnci/djac162
Abstract

Background

Personalized genomic classifiers have transformed the management of prostate cancer (PCa) by identifying the most aggressive subsets of PCa. Nevertheless, the performance of genomic classifiers to risk-classify African American men is thus far lacking in a prospective setting.

Methods

This is a prospective study of the Decipher genomic classifier for NCCN low- and intermediate-risk PCa. Study eligible non-African American men were matched to African American men. Diagnostic biopsy specimens were processed to estimate Decipher scores. Samples accrued in NCT02723734 were interrogated to determine the genomic risk of reclassification (GrR) between conventional clinical risk classifiers and the Decipher score.

Results

The final analysis included a clinically balanced cohort of 226 patients with complete genomic information (113 African American men and 113 Non-African American men). A higher proportion of African American men with NCCN-classified low- (18.2%) and favorable intermediate-risk (37.8%) PCa had a higher Decipher score than Non-African American men. Self-identified African American men were twice more likely than Non-African American men to experience GrR (relative risk [RR] = 2.23; 95% CI, 1.02-4.90; P =.04). In an ancestry-determined race model, we consistently validated a higher risk of reclassification in African American men (RR = 5.26; 95% CI, 1.66-16.63; P =.004). Race-stratified analysis of GrR vs non-GrR tumors also revealed molecular differences in these tumor subtypes.

Conclusions

Integration of genomic classifiers with clinically-based risk classification can help identify the subset of African American men with localized PCa who harbor high genomic risk of early metastatic disease. It is vital to identify and appropriately risk-stratify the subset of African American men with aggressive disease who may benefit from more targeted interventions.



Published by Oxford University Press 2022.

PMID:36053178






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