AN ASSESSMENT OF THE USEFULNESS OF SERUM PROSTATE-SPECIFIC ANTIGEN LEVEL AND CANCER VOLUME IN BIOPSY SPECIMENS TO PREDICT THE EXTENT OF PROSTATE-CANCER
K. Gohji et al., AN ASSESSMENT OF THE USEFULNESS OF SERUM PROSTATE-SPECIFIC ANTIGEN LEVEL AND CANCER VOLUME IN BIOPSY SPECIMENS TO PREDICT THE EXTENT OF PROSTATE-CANCER, British Journal of Urology, 79(4), 1997, pp. 602-607
Objective To evaluate the usefulness of the combination of serum prost
ate-specific antigen (PSA) and cancer volume in biopsy specimens as ma
rkers to predict the extent of prostate cancer. Patients and methods O
f patients presenting at our hospital with urinary symptoms suggesting
prostatic disease, 311 (median age 70 years, range 42-88) with either
nodules in the prostate detected by digital rectal examination or wit
h elevated serum PSA levels (>2.0 ng/mL) underwent systematic biopsy;
69 had prostate cancer. The cancer volume in the biopsy specimens was
examined pathologically by measuring the percentage of the biopsy core
involved with cancer, the length of cancer tissue per biopsy core and
the percentage of cancer in the biopsy specimen. The relationship of
serum PSA level, cancer volume in the biopsy specimen and the extent o
f disease was volume examined. Results The volume of cancer in the bio
psy specimens increased with increasing serum PSA concentration and th
e incidence of skeletal metastasis. The number of patients with extrap
rostatic disease or bony metastasis was significantly higher for these
Japanese patients with a serum PSA of <10 ng/mL. All six patients wit
h a positive bone scan and who had a serum PSA level of <10 ng/mL had
a larger volume of cancer in their biopsy specimens. Among patients wh
o underwent radical prostatectomy and pelvic lymphadenectomy, the inci
dence of extraprostatic disease increased with the value of each biops
y variable. Among patients with similar serum PSA levels, those showin
g higher values for the biopsy variables also showed extraprostatic di
sease. Among those with extraprostatic disease, seminal vesicles were
involved by cancer in four of six patients with >40% positivity in the
biopsy cores, >1.5 mm of cancer per biopsy core or >20% cancer in the
biopsy specimens. Lymph node metastasis was found in four of five pat
ients with serum PSA levels of >20 ng/mL and a large cancer volume in
the biopsy specimen. Conclusions These results that a combination of s
erum PSA level and cancer volume in the biopsy specimen could be usefu
l markers for predicting the extent of prostate cancer.