An observational study in Prostate Cancer, sponsored by Chinese University of Hong Kong. Completed. Open to male participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2020-04-10.
Sponsored by Chinese University of Hong Kong · Observational
Many prostate cancer patients required the use of androgen deprivation therapy (ADT) for the control of disease.
In this study, the investigators aim at assessing the different in various parameters between PCa patients received ADT and those without ADT.
60 patients diagnosed with PCa and planned for hormonal therapy will be recruited for study (active arm) and 30 PCa patients that do not planned to receive hormonal therapy (based on the clinical assessment by the investigators) will be recruited as control arm.
After written consent obtained from study subject, a series of investigation will be arranged to assess the following aspect of the subjects before the commenced of ADT:
The assessment of general condition, body composition, blood parameter and cardiovascular status will be performed every 26weeks +/- 1 weeks for two years. Bone density measurement will be performed every 52 weeks +/- 2 weeks.
Appropriate medical referral will be made if subject was found to have abnormal metabolic or cardiovascular parameters.
The prostate gland is a clinically important male accessory sex gland and vital for its production of semen. Prostate cancer (PCa) is now ranked 4th in annual incidence of male cancer and ranked 8th for cancer-related death in men in Hong Kong which accounts for about 6.2 deaths per 100,000 persons. Its incidence is rising rapidly, almost tripled in the past 10 years. As the elderly population continues to increase, the impact of PCa on the men's health and also the burden on health care system will continue to rise.
Despite the improvement in awareness of the disease and also increasing use of serum prostate specific antigen, many patients still presented at a late stage that beyond cure by local therapy. Together with those patients suffered recurrent disease after local therapy, many PCa patients required the use of androgen deprivation therapy (ADT) for the control of disease.
However, unlike other malignancy, PCa is characterized by its slow progression nature and even for metastatic disease the 5-year survival is upto 20%. Therefore, while ADT can provide effective control of disease, there are increasing evidences suggesting that it can also result in many adverse effects in the patients, and these effects are particular important due to the long survival of these patients. From the western literature, the adverse effects can be quite diverse. Classical side effects after ADT include mood changes, hot flushes, change in cognitive function, loss of libido, erectile dysfunction, osteoporosis and pathological fracture. Also there are more and more evidences showed ADT will also altered the metabolic and cardiovascular status of the patients and resulted in increase in insulin resistance and increase in risk of cardiovascular related mortality.
Traditionally, in order to achieve a complete control of PCa, ADT is given in a continue manner, either in the form of bilateral orchidectomy or regular luteinizing hormone releasing hormone injection. However, in order to balance the benefit and potential of long-term complication, intermittent hormonal therapy (IHT) become increasing common to be used in patients suffered PCa, in particular those with low tumour volume and low-grade disease. However, formal comparison of the benefit, in term of side effect reduction, for IHT compare to traditional continue-hormonal suppression is still lacking.
Unfortunately information regarding the side effects of ADT in Chinese population is lacking. However, there are some evidences from female menopause related studies that there may be some differences in the presentation and prevalence of sex hormone deprivation in difference racial groups. Therefore, there is a need to have more information on the adverse effect profiles related to ADT (both complete and IHT) in Chinese population.
6,370 studies on the registry are indexed under Prostatic Neoplasms; 1,400 are open to participants now.
This study's enrollment of 60 is below the median of 200 across 1,181 observational studies indexed under Prostatic Neoplasms.
Browse Prostatic Neoplasms studies →Chinese University of Hong Kong is the lead sponsor of 1,419 studies on the registry; 487 are open to participants now.
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60 patients diagnosed with PCa will be recruited for the study
For those received hormonal therapy will be recruited for study (active arm) Study subject inclusion criteria
For those do not plan to receive hormonal therapy (based on the clinical assessment by the investigators) will be recruited as control arm
Control subject:
Exclusion Criteria:
Study subject inclusion criteria 1. Male patients 18 years or older 2. Adenocarcinoma of the prostate either histologically or cytologically confirmed 3. Decided to be put on ADT -bilateral orchidectomy or luteinizing hormone-releasing hormone (LHRH) agonist or LHRH antagonist, with or without additional antiandrogen 4. After ADT performed, serum testosterone level should reach castrated level, i.e. \< 50 ng/dL after 6 weeks of treatment 5. Able to consent for the participate in the study
Other: It is an observational study.
Control subject: 1. Male patients 18 years or older 2. Adenocarcinoma of the prostate either histologically or cytologically confirmed 3. Able to consent for the participate in the study
Change from Baseline cardiovascular risk at 24 months
Measured by Framingham risk score (Estimation of 10-year Cardiovascular Disease Risk in percentage)
Time frame: At baseline and month-24
Change from Baseline total cholesterol at 24 months
Measured by total cholesterol blood test
Time frame: At baseline and month-24
Change from Baseline low density lipoprotein at 24 months
Measured by low density lipoprotein blood test
Time frame: At baseline and month-24
Change from Baseline high-density lipoprotein at 24 months
Measured by high-density lipoprotein blood test
Time frame: At baseline and month-24
Change from Baseline triglyceride at 24 months
Measured by triglyceride blood test
Time frame: At baseline and month-24
Change from Baseline body mass index (BMI) at 24 months
Weight and height will be combined to report BMI in kg/m\^2
Time frame: At baseline and month-24
Change from Baseline body composition at 24 months
Measured by percentage of body fat
Time frame: At baseline and month-24
Change from Baseline mental state at 24 months
Measured by the General Practitioner assessment of Cognition (GPCOG). Range of total score: 0-9, higher score mean less cognitive impairment (ie. better outcome).
Time frame: At baseline and month-24
Change from Baseline vascular arterial stiffness at 24 months
Vascular arterial stiffness measured by Pulse Wave Velocity (m/s) using non-invasive vascular screening device
Time frame: At baseline and month-24
Change from Baseline ankle brachial index (ABI) at 24 months
ABI (ratio of the blood pressure at the ankle to the blood pressure in the upper arm) measured by using non-invasive vascular screening device
Time frame: At baseline and month-24
Compare cardiovascular events
Measured by the cardiovascular adverse event rate
Time frame: At month-24
Change from Baseline bone mineral density at 24 months
Bone mineral density measured by using bone density scanning device
Time frame: At baseline and month-24
Compare skeletal related events
Measured by the fracture rate
Time frame: At month-24
No study locations are listed for this record.
This study is completed, as verified in Apr 2020. You cannot join it, but the record below documents what was studied.
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Chinese University of Hong Kong