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Prostate Cancer
Prostate Cancer Overview Adenocarcinoma of the prostate is the clinical term for a cancerous tumor on the prostate gland. As prostate cancer grows, it may spread to the interior of the gland, to tissues near the prostate, to sac-like structures attached to the prostate (seminal vesicles), and to distant parts of the body (e.g., bones, liver, lungs). Prostate cancer confined to the gland often is treated successfully. Anatomy Incidence and Prevalence Prostate cancer occurs in 1 out of 6 men. Reports of diagnosed cases have risen rapidly in recent years and mortality rates are declining, which may be due to increased screening. African American men have the highest incidence of prostate cancer, and Asian and Native American men have the lowest incidence. Rates for Asian and African men increase sharply when they emigrate to the United States, suggesting an environmental connection (e.g., high-fat diet, smoking). The risk for developing prostate cancer rises significantly with age, and 60% of newly diagnosed cases occur in men over the age of 70. A family history of prostate cancer increases the risk. Other possible risk factors include the following:
Early prostate cancer usually is discovered during a routine digital rectal examination (DRE) or PSA screening. Early prostate cancer rarely causes symptoms. However, men observing the following signs and/or symptoms should see their physician for a thorough examination.
Diagnosis Several tests are used to diagnose prostate cancer. Digital Rectal Examination In a DRE, the physician inserts a lubricated, gloved finger into the rectum to feel the surface of the prostate gland. Healthy prostate tissue is soft, like the fleshy tissue of the hand where the thumb joins the palm. Malignant tissue is firm, hard, and often asymmetrical or stony, like the bridge of the nose. However, as many as one-third of patients diagnosed with prostate cancer have a normal DRE. Transrectal ultrasound (TRUS) TRUS and the digital rectal examination are effective prostate-cancer screening tools. PSA and PAP Tests Blood tests taken to check the levels of prostate specific antigen (PSA) and prostatic acid phosphatase (PAP) in a patient who may have benign prostatic hyperplasia help the physician eliminate or confirm a diagnosis of prostate cancer. Prostate-specific antigen (PSA) is produced by the cells of the prostate capsule (membrane covering the prostate) and periurethral glands. Patients with benign prostatic hyperplasia (BPH) or prostatitis produce greater amounts of PSA. The PSA level also is determined in part by the size and weight of the prostate. The test measures the amount of PSA in the blood in nanograms per milliliter (ng/mL). A PSA of 4 ng/mL or lower is considered normal; 4 - 10 ng/mL, slightly elevated; 10 - 20, moderately elevated; and 20 - 35, highly elevated. Most men with slightly elevated PSA levels do not have prostate cancer, and many men with prostate cancer have normal PSA levels. A highly elevated level may indicate the presence of cancer. The PSA test can produce false results. A false positive result occurs when the PSA level is elevated and there is no cancer. A false negative result occurs when the PSA level is normal and there is cancer. Because of this, a biopsy is usually performed to confirm or rule out cancer when the PSA level is high. Free and total PSA (also known as PSA II) Age-specific PSA Use the PSA Age/Race HealthProfiler or the PSA Velocity HealthProfiler to determine your risk of prostate cancer. Prostatic acid phosphatase (PAP) test Tumor Biopsy If a tumor is found, a biopsy is performed to determine the type of cancer, its location, and stage of development. Before undergoing the biopsy, patients should abstain from alcohol, aspirin, and nonsteroidal anti-inflammatory drugs (e.g., ibuprofen) for 1 week. They are required to take one Fleet enema the night before the procedure and one 2 hours before the biopsy. An oral antibiotic (usually ciprofloxacin) is prescribed to be taken the day before, the day of, and 2 days after the biopsy. The biopsy is performed with the patient lying on his side with his knees brought up to his chest. A biopsy needle, similar to one used to draw blood or administer injections, is inserted through the perineum into the tumor. A probe, guided by transrectal ultrasound (TRUS), is inserted into the rectum to help the physician properly place the needle, which is projected through the tip of the probe. A cell sample is extracted from one or several areas of the tumor into the syringe. The sample(s) is analyzed by a pathologist to confirm the diagnosis of a cancerous tumor and determine its type. The results are obtained within 5-10 working days. Gleason score The pathologist examines two tissue samples taken from different areas of the tumor and assigns a score of 1 to 5 to each sample. The more abnormal the tissue, the higher the score. The sum of the two produces the Gleason score. Gleason scores of 2 to 4 indicate that the cells are well differentiated, meaning the tissue is not too abnormal; 5 to 7 moderately differentiated; 8 to 10 poorly differentiated. Higher scores suggest aggressive tumors that likely require aggressive treatment. Complications If the patient develops a large number of blood clots or cannot urinate, the physician should be contacted or the patient should go to the emergency room. Rarely, biopsy of a cancerous tumor also may cause spreading, or "seeding," of cancer cells along the path of the biopsy needle. Computed tomography (CT scan) Bone scan
Staging The physician "stages" the tumor based on its size, the character of its cells, and the extent of metastisis. Two systems commonly are used for staging prostate cancer: the Jewett-Whitmore system and the TNM (tumor, node, metastases) system. Jewett-Whitmore system Stage A
Stage B
Stage C
Stage D
TNM System Primary tumor (T)
Regional Lymph Nodes (N)
Distant Metastasis (M)
Medical Treatment Treatment for prostate cancer depends on the stage of the disease and the patient's age and overall health. Elderly patients with minor symptoms, early stage cancer, or coexisting illness may be treated conservatively. Watchful waiting is a reasonable course of action for patients who are elderly, in poor health, or with early stage cancer. Untreated prostate cancer may take years to become problematic. During this time, the physician monitors the patient's condition for any marked or sudden progression of the disease, which may signal the need for more aggressive treatment.
Hormone Therapy Viadur® is a matchstick-sized titanium pump inserted under the skin on the upper arm that delivers a constant rate of leuprolide acetate for 1 year. This prostate cancer treatment suppresses androgen (e.g., testosterone, estrogen) production, causing the tumor to shrink or stop growing and reducing symptoms (e.g., pain, urinary retention, urinary frequency). A tablet located in one end of the implant draws moisture from surrounding tissue in the arm. The moisture exerts pressure within the device that steadily pushes medication from the other end. The device is inserted under local anesthesia through a small incision. The incision must be kept dry for 24 hours and must remain bandaged for a few days. Strenuous physical activity should be avoided for 48 hours. The implant is removed after 12 months and a new device may be inserted. Side effects associated with hormone therapy include the following:
Patients may also experience an increase in prostate cancer symptoms for approximately 2 weeks, due to a temporary increase in testosterone levels. Patients with advanced disease (e.g., large bone, bladder, or spinal cord tumors) may be unable to tolerate this increase in testosterone. Studies have shown that abarelix injection (Plenaxis™), which does not cause a surge in testosterone, can be used in some of these patients to relieve symptoms (e.g., bone pain, inability to urinate). Plenaxis may cause life-threatening conditions in some people, such as a drop in blood pressure; loss of consciousness; breathing problems (e.g., shortness of breath, wheezing); and swelling of the face, eyelids, tongue, or throat. Patients must be monitored by a physician for at least 30 minutes after each administration of the drug in case an adverse reaction does occur. Treatment involves one injection into the buttocks every 2 weeks for the first month, and every 4 weeks thereafter. Blood tests are performed every 2 months to monitor the effectiveness of the drug. Common side effects include the following:
Zoledronic acid (Zometa®) is a bisphosphonate prescribed to treat hypercalcemia-excess calcium in the blood-in prostate cancer patients who have bone metastases (secondary tumors in bone). Patients with hypercalcemia experience dehydration, fatigue, nausea, vomiting, confusion, and if untreated, may result in coma. Bone metastases cause bone tissue to break down, which releases calcium into the bloodstream. Zoledronic acid increases bone density, decreases bone loss, and reduces the risk for fractures. Patients must have completed at least one course of hormone therapy before starting this treatment. Doses are given intravenously for 15 minutes, every 3 to 4 weeks. A blood sample is taken before each treatment to monitor kidney function. Zoledronic acid is not recommended for patients with severe kidney disease and should be used with caution in those with aspirin-sensitive asthma and those taking loop diuretics (e.g., hydrochlorothiazide). Side effects usually are mild and temporary. Patients may experience the following:
Two types of radiation therapy are used to treat prostate cancer: brachytherapy and external radiation therapy (XRT). Brachytherapy Transrectal ultrasound (TRUS) is used to create a three-dimensional grid map of the prostate, and a computer calculates the volume of the gland, the number of seeds needed, and determines where they will be placed. The procedure is performed on an outpatient basis and takes 45 to 60 minutes. The patient is given regional anesthesia. A needle is inserted through the perineum and into the predetermined site(s). Fifty to 100 rice-sized seeds are implanted into the prostate through the needle. The seeds contain a radioactive isotope (usually palladium 103 or iodine 125) that emits radiation for about 3 months and then becomes inert. Recovery Complications External Radiation Treatment (XRT) A study of 999 patients found 79% of stage T1, 66% of stage T2, 55% of stage T3, and 22% of stage T4 prostate cancer patients survived 10 years after XRT. Complications Surgery Good candidates for surgery to treat prostate cancer have one or more of the following characteristics:
Depending on the extent of the disease, there are several surgical options for prostate cancer. Cryosurgery This minimally invasive outpatient procedure, also called cryoablation, destroys cancer cells by twice rapidly freezing and thawing cancerous tissue. It is recommended for patients who
Transrectal ultrasound and prostate biopsy are performed prior to cryosurgery to determine the exact size and location of the tumor(s). The procedure is performed under regional (e.g., epidural nerve block) or general anesthesia. With the man on his back, the surgeon inserts a warming catheter into the urethra to protect it from freezing temperatures. An ultrasound transducer is inserted into the rectum, so the surgeon can see the prostate and surrounding tissue and monitor placement of the cryoprobes. The surgeon then makes 5 to 8 needle punctures in the perineum and advances the needles to preselected locations in the prostate tumor. Liquid nitrogen or argon gas circulates through the probes and freezes cancer cells to -40°C. The tem Content © Copyright Urology
Channel 2008
http://www.uclaurology.com/site_uo/pdf/PCI_long_1.pdfProstate cancer is the most common type of cancer found in men, and is one of the most treated at UCLA. The most typical symptom of prostate cancer is no symptom at all. With early detection and treatment, your chances of surviving prostate cancer are greatly improved. Prostate cancer is more common in African American men and in men with a father or brother with prostate cancer. UCLA Oversses IMPACT Program (www.california-impact.org) IMPACT: Improving Access, Counseling and Treatment for Californians with Prostate Cancer is a statewide program that helps uninsured men with prostate cancer receive critical medical care. The three-year program, administered by UCLA, is funded with $50 million from the State of California. Dr. Mark S. Litwin and Dr. James R. Orecklin from the UCLA Department of Urology oversee the program statewide. IMPACT targets men at risk of prostate cancer regardless of age, and who have no or limited health insurance, do not qualify for Medi-Cal, do not have Medicare and have incomes under 200 percent of the federal poverty level. In addition to offering treatment, the program promotes awareness about the importance of timely, high quality prostate cancer treatment. Regional sites offering IMPACT services have opened at the University of California campuses in San Francisco, Irvine, San Diego, and the UC Davis campus in Sacramento. Prostate Cancer Index Developed by Mark Litwin, M.D., M.P.H., the UCLA Prostate Cancer Index is considered worldwide to be the standard in measuring outcomes and quality of life in prostate cancer survivors. The Index is now used in over 200 studies throughout North America. To download your own copy, please click on any of the following links: UCLA Prostate Cancer Index
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