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. 2020 Sep 10;383(11):1083-1085.
doi: 10.1056/NEJMc2000069.

Racial Differences in Genomic Profiling of Prostate Cancer

Affiliations

Racial Differences in Genomic Profiling of Prostate Cancer

Brandon A Mahal et al. N Engl J Med. .
No abstract available

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Figures

Figure 1.
Figure 1.. Tumor-Mutation Profiles in the 2393 Study Patients.
Shown are tumor-mutation profiles according to race among men with primary prostate cancer (Panels A, C, and E) or metastatic prostate cancer (Panels B, D, and F). The data were obtained from targeted tumor-sequencing testing available to patients at the Memorial Sloan Kettering (MSK) Cancer Center (Integrated Mutation Profiling of Actionable Cancer Targets [IMPACT]) and from the Dana–Farber Cancer Institute (Oncopanel next-generation sequencing). (Details regarding testing methods are provided in the Supplementary Appendix.) Among the 2393 patients who were included in the study, 1484 patients had primary tumors, and 909 patients had metastatic tumors. The total mutation count in the two subgroups (Panels A and B) was calculated in the MSK-468 cohort (the largest subgroup in the study), in which patients were evaluated on a next-generation sequencing panel of 468 unique genes. Mutational frequency is shown for the genes that were most commonly altered in the study (Panels C and D). Actionable mutations are alterations that are the intended targets of precision-oncology drugs. Genes with actionable mutations (Panels E and F) include ABL1, EGFR, ERBB2, BRAF, BRCA1/2, FGFR2/3, KIT, NTRK1/2/3, PDGFRA, RET, ROS1, ALK, and PIK3CA. Among the patients with metastatic prostate cancer, genes with actionable mutations occurred more often in Black men than in White men (26.7% vs. 18.0%, P=0.05). DNA-repair genes include ERCC5, MRE11, TP53BP1, POLE, RAD21, MSH2, MSH6, BRCA1/2, ATR, and ATM. Mutations in DNA-repair genes occurred more often in Black men than in White men (22.5% vs. 15.6%, P=0.05) among those with metastatic disease.

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