The Journal of Urology · 2020 · 36 citations · 0 references
MedicineOncologyUrologyGenitourinary OncologyGenomicsMolecular OncologyCancer GenomicsCirculating Tumor Dna AnalysisDna SequencingGenomic ProfilingNext-generation Sequencing In OncologyProstate CancerCastration-resistant Prostate Cancer TherapyCirculating Tumor Cell Genomic AnalysisCirculating Tumor Dna SequencingCirculating Tumor Dna TestingGenomic Alteration ProfilingSomatic Genomic AlterationsTumor Genomic ProfilingTumor Mutational Profiling
PURPOSE: To explore the genomic profiles of Chinese patients with castration sensitive prostate cancer and those with metastatic castration resistant prostate cancer via germline and circulating tumor DNA sequencing. MATERIALS AND METHODS: . RESULTS: (36.8% vs 15.3%, p <0.001) in our metastatic castration resistant prostate cancer cohort compared with the SU2C-PCF (Stand Up to Cancer-Prostate Cancer Foundation) cohort. Alteration frequencies of DNA damage repair pathway genes (66.7% vs 41.5%, p=0.015) and androgen receptor pathway genes (71.9% vs 48.8%, p=0.018) in patients with metastatic castration resistant prostate cancer were higher than in patients with de novo metastatic castration sensitive prostate cancer. Androgen receptor alteration was selectively enriched in metastatic castration resistant prostate cancer. CONCLUSIONS: were observed in our metastatic castration resistant prostate cancer cohort than in the SU2C-PCF cohort. Our findings support the view that circulating tumor DNA sequencing could guide clinical treatment for metastatic prostate cancer.