Clinical Trials Logo

Clinical Trial Summary

Osteoporosis, or thinning of the bones is a common disorder which can cause significant morbidity in terms of pain and fracture. One of the causes of osteoporosis is a low or absent testosterone level. Prostate cancer is the second most common malignancy in males with an increasing incidence. The mainstay of advanced prostate cancer treatment is hormonal manipulation (surgery or medications) in order to lower testosterone levels as testosterone stimulates cancer cells. Despite the known links both between osteoporosis, low testosterone, and prostate cancer, little data is available on how common osteoporosis is among men with advanced prostate cancer treated with hormonal manipulation. Since prostate cancer affects so many men and the indications for early hormonal manipulation are expanding, it is important to determine the prevalence of osteoporosis in these males.


Clinical Trial Description

INTRODUCTION - Osteoporosis is a common disorder with many predisposing factors including hypogonadism from a variety of causes. Prostate cancer is the second most common malignancy in men. The standard treatment for men with advanced prostate cancer is hormonal manipulation in order to decrease testosterone levels which renders a man hypogonadal. There is an increasing body of literature that suggests men with prostate cancer treated with hormonal manipulation develop osteoporosis and associated complications more commonly than aged matched controls. With the increasing incidence of prostate cancer and the increasing indications with hormonal therapy use in advanced prostate cancer, osteoporosis in these men is a major health concern.Hormonal manipulation in order to obtain castrate levels of testosterone can be achieved with bilateral orchiectomy, Luteinizing Hormone Releasing Hormone agonists (LHRHA) and steroidal antiandrogens combined with mini doses of estrogen based therapy. Nonsteroidal antiandrogens are also used in the management of advanced prostate cancer however, on their own, are not enough to suppress testosterone. The data on exactly how common and severe a problem osteoporosis is in men treated with different forms of hormonal manipulation is sparse and because of the lack of data, there is currently no accepted standard of care in the investigation and management of osteoporosis in these men. The researchers propose to start with a pilot study to first determine the prevalence of osteoporosis in 6 different populations of men with advanced prostate cancer, (1) newly diagnosed, (2) treated with orchiectomy, (3) treated with an LHRHA, (4) treated with steroidal antiandrogen therapy, (5) treated with nonsteroidal antiandrogen based therapy, (6) treated with complete androgen blockade (LHRHA plus a nonsteroidal antiandrogen).

OBJECTIVES - To determine, in the above populations, the bone mineral density as measured by Dual Energy X-ray Absorptiometry (DEXA) of the lumbar spine, proximal hip (total hip, femoral neck and trochanter), and non-dominant distal radius, to document biochemical markers of bone turnover, to document vertebral fractures and body height, to document other aspects of body composition including adipose tissue and muscle mass as measured by whole body composition densitometry, and to document other potential confounding factors predisposing prostate cancer patients to osteoporosis.

STUDY DESIGN - This primarily will be a descriptive, exploratory study describing the prevalence of osteoporosis in each of the 6 groups defined above. The diagnosis of osteoporosis will be based on bone densitometry studies. There are accepted densitometric criteria for the assessment of normal and abnormal bone mass. The criteria were largely developed in postmenopausal Caucasian women but reference values are also available for Caucasian, Black and Hispanic men. Normal bone density is described as a T-score less than -1. T-scores between -1 and -2.5 are indicative of osteopenia, and T-scores of less than -2.5 are indicative of osteoporosis. The prevalence of osteoporosis (T value less than 2.5) in each of the groups will be reported. Information on biochemical markers of bone turnover, vertebral fractures, and other risk factors will also be described.

PATIENT SELECTION - Patients with biopsy proven advanced prostate cancer, no known prior clinical or radiographic history of osteoporosis, minimum of 1 year of hormonal therapy in arms 2, 3, 4, 5 and 6, and an ability and willingness to give informed consent. Exclusion criteria - Patients with known bone disorders other than metastatic disease such as hyperparathyroidism, Paget's disease, renal osteodystrophy, and documented osteomalacia as well as osteoporosis, patients who have received a bisphosphonate, systemic fluoride, pharmacological doses of calcium (less than 1500 mg/day) or Vitamin D (less than 1000 IU/day), or calcitonin, patients with known abnormal thyroid function, and patients with marked renal impairment (creatinine less than 2.0 X normal).

MANAGEMENT OF PATIENTS - This will be an outpatient study. All patients will initially be assessed by a research nurse and/or physician at the Cross Cancer Institute with a prostate cancer specific history, blood and urine tests. Patients will be referred to a single endocrinologist for a more detailed osteoporosis history and physical exam. On the same day, they will have a densitometry study, whole body composition study, and plain radiographs taken. Patients will then be seen at the Cross Cancer Institute to discuss their results. Should a diagnosis of osteoporosis be made, a letter indicating this will be sent to the patient's family physician.

ENDPOINTS - The primary endpoint will be bone mineral density. Osteoporosis will be diagnosed if the T value is less than -2.5. The secondary endpoints will be - biochemical markers of bone turnover, vertebral fractures, vertebral body height, body composition of fat, body composition of adipose tissue.

DATA ANALYSIS - The data will be entered into a computerized database. Descriptive statistics will be tabulated for all 5 arms being studied with respect to demographic variables, baseline characteristics, and test results. ;


Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT00124410
Study type Observational
Source AHS Cancer Control Alberta
Contact
Status Completed
Phase N/A
Start date January 2000

See also
  Status Clinical Trial Phase
Recruiting NCT05613023 - A Trial of 5 Fraction Prostate SBRT Versus 5 Fraction Prostate and Pelvic Nodal SBRT Phase 3
Recruiting NCT05540392 - An Acupuncture Study for Prostate Cancer Survivors With Urinary Issues Phase 1/Phase 2
Recruiting NCT05156424 - A Comparison of Aerobic and Resistance Exercise to Counteract Treatment Side Effects in Men With Prostate Cancer Phase 1/Phase 2
Completed NCT03177759 - Living With Prostate Cancer (LPC)
Completed NCT01331083 - A Phase II Study of PX-866 in Patients With Recurrent or Metastatic Castration Resistant Prostate Cancer Phase 2
Recruiting NCT05540782 - A Study of Cognitive Health in Survivors of Prostate Cancer
Active, not recruiting NCT04742361 - Efficacy of [18F]PSMA-1007 PET/CT in Patients With Biochemial Recurrent Prostate Cancer Phase 3
Completed NCT04400656 - PROState Pathway Embedded Comparative Trial
Completed NCT02282644 - Individual Phenotype Analysis in Patients With Castration-Resistant Prostate Cancer With CellSearch® and Flow Cytometry N/A
Recruiting NCT06037954 - A Study of Mental Health Care in People With Cancer N/A
Recruiting NCT06305832 - Salvage Radiotherapy Combined With Androgen Deprivation Therapy (ADT) With or Without Rezvilutamide in the Treatment of Biochemical Recurrence After Radical Prostatectomy for Prostate Cancer Phase 2
Recruiting NCT05761093 - Patient and Physician Benefit/ Risk Preferences for Treatment of mPC in Hong Kong: a Discrete Choice Experiment
Completed NCT04838626 - Study of Diagnostic Performance of [18F]CTT1057 for PSMA-positive Tumors Detection Phase 2/Phase 3
Recruiting NCT03101176 - Multiparametric Ultrasound Imaging in Prostate Cancer N/A
Completed NCT03290417 - Correlative Analysis of the Genomics of Vitamin D and Omega-3 Fatty Acid Intake in Prostate Cancer N/A
Completed NCT00341939 - Retrospective Analysis of a Drug-Metabolizing Genotype in Cancer Patients and Correlation With Pharmacokinetic and Pharmacodynamics Data
Completed NCT01497925 - Ph 1 Trial of ADI-PEG 20 Plus Docetaxel in Solid Tumors With Emphasis on Prostate Cancer and Non-Small Cell Lung Cancer Phase 1
Recruiting NCT03679819 - Single-center Trial for the Validation of High-resolution Transrectal Ultrasound (Exact Imaging Scanner ExactVu) for the Detection of Prostate Cancer
Completed NCT03554317 - COMbination of Bipolar Androgen Therapy and Nivolumab Phase 2
Completed NCT03271502 - Effect of Anesthesia on Optic Nerve Sheath Diameter in Patients Undergoing Robot-assisted Laparoscopic Prostatectomy N/A