Abstract:
ABSTRACT
Background: Prostate cancer is the second most common cancer in men and 6th leading cause
of mortality. If not recognized early, patients with advanced disease can get debilitating
complications such as spinal cord compression and fractures which can otherwise be prevented
by early androgen deprivation therapy. Our research intends to contribute more knowledge
about the practical approach to the management of advanced prostate cancer in the community
for the prevention of debilitating complications.
Objectives: To determine clinical parameters and PSA threshold for effective clinical
diagnosis of advanced prostate cancer in the community.
Methods: A prospective cross-sectional observational study was conducted at three referral
hospitals in Kigali on patients who presented with clinical suspicion of advanced prostate
cancer from October 2018 to February 2019. All patients underwent prostate biopsy as well as
metastatic work up, for those who were eligible. Statistical analysis was done using STATA
14.2.
Results: During the study period, we enrolled 114 patients. The median age was 70 years (IQR
65-79 years) and mean (±SD) age was 71 ± 9 years; 75 (65.8 %) patients were enrolled from
CHUK, 35 (30.7%) from RMH and 4 (3.5%) from KFH. In total 14 (12.3%) patients and 100
(87.7%) patients were found to have benign disease and cancer respectively. Among those who
had cancer, 85 (85%) had advanced prostate cancer (locally advanced and metastatic); All the
10.5% of patients with family history of prostate cancer were positive (both first and second
level) however, 34.2% of respondents didn’t remember about family history of prostate cancer;
75.5% were unemployed or not working because of the illness; 110/114 (96.5%) were
symptomatic at presentation while 3/4 were discovered through systematic screening.
Common presenting symptoms were: lower urinary tract symptoms (80.7%), back pain
(54.4%) and urine retention (36.8%). All patients with paraplegia had advanced cancer and all
who reported weight loss had cancer. The mean duration of symptoms before consultation was
14.2 months. On DRE examination, 102/114 patients were found to have abnormal prostate
with at least one palpable nodule and 75.3% had multinodular prostate which involved both
lobes in 71 (70.3%) patients. Abnormal digital rectal examination (DRE) was a strong risk
factor for both cancer and advanced disease. Prostate cancer was found in 92.2% of those with
abnormal DRE compared to 41.7% in those with normal DRE (p=0.001). Also, cancer was
significantly found in 96.1% of those with multinodular prostate (p=0.02) and had high odds
(OR: 14.6; CI 3.41-62.25) of having advanced prostate cancer (p<0.001). The mean (±SD) PSA
was 643.3 ± 1829.8 ng/ml and the median (range) was 100 ng/ml (9.05-10,000ng/ml) for the
whole study population. PSA levels of patients with histologically confirmed benign disease
had a mean of 35.8ng/ml (9.05 - 98.5ng/ml) and none had PSA> 100ng/ml. Patients with
localized prostate cancer had mean PSA of 66.3ng/ml while those with advanced prostate
cancer had mean PSA of 841.4 ng/ml respectively. All patients with PSA of 100 ng/ml or above
had cancer and advanced prostate cancer. 49/85 that had complete metastatic workup had bone
metastasis; 77.5% had back pain (p=0.001) and 47/49 had abnormal DRE.
Conclusion: The results show that there is a significant correlation between back pain and
bone metastasis in patients with prostate cancer. All patients with abnormal DRE and PSA
above 100 ng/ml had advanced prostate cancer. There is correlation between back pain,
abnormal DRE and PSA above 100 ng/ml with advanced cancer and bone metastasis.