Practical Utility of Liquid Biopsies for Evaluating Genomic Alterations in Castration-Resistant Prostate Cancer

Author:

Jeong Seung-Hwan1,Kyung Dongsoo2,Yuk Hyeong Dong1ORCID,Jeong Chang Wook1,Lee Wookjae2,Yoon Jung-Ki2,Kim Hwang-Phill2,Bang Duhee3,Kim Tae-You245,Lim Yoojoo2ORCID,Kwak Cheol1

Affiliation:

1. Department of Urology, Seoul National University Hospital, Seoul 03080, Republic of Korea

2. IMBdx Inc., Seoul 08506, Republic of Korea

3. Department of Chemistry, Yonsei University, Seoul 03722, Republic of Korea

4. Department of Internal Medicine, Seoul National University Hospital, Seoul 03080, Republic of Korea

5. Cancer Research Institute, Seoul National University Hospital, Seoul 03080, Republic of Korea

Abstract

Traditional tissue-based assessments of genomic alterations in castration-resistant prostate cancer (CRPC) can be challenging. To evaluate the real-world clinical utility of liquid biopsies for the evaluation of genomic alterations in CRPC, we preemptively collected available plasma samples and archival tissue samples from patients that were being treated for clinically confirmed CRPC. The cell-free DNA (cfDNA) and tumor tissue DNA were analyzed using the AlphaLiquid®100-HRR panel. Plasma samples from a total of 87 patients were included in this study. Somatic mutations from cfDNA were detected in 78 (89.7%) patients, regardless of the presence of overt metastasis or concomitant treatment given at the time of plasma sample collection. Twenty-three patients were found to have known deleterious somatic or germline mutations in HRR genes from their cfDNA. Archival tissue samples from 33 (37.9%) patients were available for comparative analysis. Tissue sequencing was able to yield an NGS result in only 51.5% of the tissue samples. The general sensitivity of cfDNA for detecting somatic mutations in tissues was 71.8%, but important somatic/germline mutations in HRR genes were found to have a higher concordance (100%). Liquid biopsies can be a reasonable substitute for tissue biopsies in CRPC patients when evaluating genomic alterations.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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