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. 2021 Aug 28;13:168. doi: 10.1186/s13148-021-01155-w

Table 1.

Clinical characteristics of the study cohort (n = 9)

Mean agea, years (range) 64.2 (51–74)
Gleason score at diagnosisb, n (%)
7 (3 + 4) 5 (55.6)
9 4 (44.4)
Metastatic sites, n (%)
Bone 9 (100)
Lymph node 2 (22.2)
Evidence of castration resistance at recruitment (cohort)c, n (%)
No (mPCa; cohort 1) 5 (55.6)
Yes (mCRPC; cohort 2) 4 (44.4)
Number of timepointsd, n (%)
4 2 (22.2)
5 2 (22.2)
6 5 (55.6)
Mean cfDNA concentratione, ng/ul (range) 5.08 (0.61–38)
Mean PSA levelse, ng/ml (range) 35.3 (0.1–352.1)
Therapies administeredf, n (%)
LHRH agonists/antagonists 8 (88.9)
Taxanes 9 (100)
AR-inhibitors 8 (88.9)
Radioisotopes 3 (33.3)
Mean follow-up timeg, months (range) 19.1 (13–21)

AR androgen receptor, cfDNA cell-free DNA, LHRH Luteinizing hormone-releasing hormone, mPCa metastatic prostate cancer, mCRPC metastatic castration resistant prostate cancer, PSA prostate-specific antigen

Other notes: aAge at time of recruitment

bPrior to recruitment

cCohort classification: Cohort 1—patient was on/starting androgen deprivation therapy at time of recruitment, and had no evidence of castration resistance; Cohort 2—patient had castration resistant disease at time of recruitment

dTimepoint refers to number of cfDNA isolations available for study

eAt any given timepoint

fDuring follow-up in the iPROSPECT study

gFollow-up time reflects last timepoint obtained for this analysis