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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Active arm: Subjects received hormonal therapy | Study subject inclusion criteria
|
| |
| Control arm: Subjects do not plan to receive hormonal therapy | Control subject:
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| It is an observational study. | Other |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change from Baseline cardiovascular risk at 24 months | Measured by Framingham risk score (Estimation of 10-year Cardiovascular Disease Risk in percentage) | At baseline and month-24 |
| Measure | Description | Time Frame |
|---|---|---|
| Change from Baseline total cholesterol at 24 months | Measured by total cholesterol blood test | At baseline and month-24 |
| Change from Baseline low density lipoprotein at 24 months | Measured by low density lipoprotein blood test |
Not provided
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:
Only mole can develop prostate cancer
60 patients diagnosed with PCa will be recruited for the study
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| Name | Affiliation | Role |
|---|---|---|
| Chi Fai NG, MD | Chinese University of Hong Kong | Principal Investigator |
Not provided
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 17132744 | Background | Beauchet O. Testosterone and cognitive function: current clinical evidence of a relationship. Eur J Endocrinol. 2006 Dec;155(6):773-81. doi: 10.1530/eje.1.02306. | |
| 20923031 | Background | Fang LC, Merrick GS, Wallner KE. Androgen deprivation therapy: a survival benefit or detriment in men with high-risk prostate cancer? Oncology (Williston Park). 2010 Aug;24(9):790-6, 798. |
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| ID | Term |
|---|---|
| D011471 | Prostatic Neoplasms |
| ID | Term |
|---|---|
| D005834 | Genital Neoplasms, Male |
| D014565 | Urogenital Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
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Blood for fasting lipid, sugar, hsCRP and other hormones (about 15cc) will be assessed in each study visit.
| At baseline and month-24 |
| Change from Baseline high-density lipoprotein at 24 months | Measured by high-density lipoprotein blood test | At baseline and month-24 |
| Change from Baseline triglyceride at 24 months | Measured by triglyceride blood test | 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 | At baseline and month-24 |
| Change from Baseline body composition at 24 months | Measured by percentage of body fat | 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). | 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 | 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 | At baseline and month-24 |
| Compare cardiovascular events | Measured by the cardiovascular adverse event rate | At month-24 |
| Change from Baseline bone mineral density at 24 months | Bone mineral density measured by using bone density scanning device | At baseline and month-24 |
| Compare skeletal related events | Measured by the fracture rate | At month-24 |
| 20224416 | Background | Lattouf JB, Saad F. Bone complications of androgen deprivation therapy: screening, prevention, and treatment. Curr Opin Urol. 2010 May;20(3):247-52. doi: 10.1097/MOU.0b013e32833835be. |
| 20124128 | Background | Levine GN, D'Amico AV, Berger P, Clark PE, Eckel RH, Keating NL, Milani RV, Sagalowsky AI, Smith MR, Zakai N; American Heart Association Council on Clinical Cardiology and Council on Epidemiology and Prevention, the American Cancer Society, and the American Urological Association. Androgen-deprivation therapy in prostate cancer and cardiovascular risk: a science advisory from the American Heart Association, American Cancer Society, and American Urological Association: endorsed by the American Society for Radiation Oncology. Circulation. 2010 Feb 16;121(6):833-40. doi: 10.1161/CIRCULATIONAHA.109.192695. Epub 2010 Feb 1. No abstract available. |
| 18853115 | Background | Rampp T, Tan L, Zhang L, Sun ZJ, Klose P, Musial F, Dobos GJ. Menopause in German and Chinese women--an analysis of symptoms, TCM-diagnosis and hormone status. Chin J Integr Med. 2008 Sep;14(3):194-6. doi: 10.1007/s11655-008-0194-1. Epub 2008 Oct 14. |
| 19286225 | Background | Saylor PJ, Smith MR. Metabolic complications of androgen deprivation therapy for prostate cancer. J Urol. 2009 May;181(5):1998-2006; discussion 2007-8. doi: 10.1016/j.juro.2009.01.047. Epub 2009 Mar 14. |
| 18790986 | Background | Smith MR. Treatment-related diabetes and cardiovascular disease in prostate cancer survivors. Ann Oncol. 2008 Sep;19 Suppl 7(Suppl 7):vii86-90. doi: 10.1093/annonc/mdn458. No abstract available. |
| 19399748 | Background | Taylor LG, Canfield SE, Du XL. Review of major adverse effects of androgen-deprivation therapy in men with prostate cancer. Cancer. 2009 Jun 1;115(11):2388-99. doi: 10.1002/cncr.24283. |
| D005832 |
| Genital Diseases, Male |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D011469 | Prostatic Diseases |
| D052801 | Male Urogenital Diseases |