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Prostate Cancer Screening Guidelines
In 2012, the United States Preventive Services Task Force (USPSTF) recommended against prostate cancer screening for all men, regardless of age, who do not have symptoms. The USPSTF based its recommendations on concerns regarding the prostate-specific antigen (PSA) blood test. According to the USPSTF, evidence indicates that PSA screening offers “a very small potential benefit and significant potential harm” from unnecessary treatment.
The American Cancer Society’s guidelines for early detection of prostate cancer recommend that men discuss with their doctors the uncertainties, risks, and potential benefits of screening for prostate cancer before deciding whether to be tested. In 2013, the American Urological Association and the American College of Physicians released similar guidelines, which no longer recommend the PSA test for men at average risk who are younger than age 55 or older than age 69.
Debate continues over whether the benefits of prostate specific antigen (PSA) screening outweigh the treatment risks for most men. In general, the current consensus is that there is no "one size fits all" guideline for who should receive prostate cancer screening and at what age. It is important to discuss with your doctor your questions and concerns regarding prostate cancer screening.
Genetic Tests for Prostate Cancer
New genetic tests are being developed to help doctors determine whether a man’s prostate cancer is aggressive or low-risk. By predicting if a cancer is likely to grow and spread, these tests may be able to spare some men from unnecessary treatment. Within the next year, about a dozen of these types of tests will become available. Genetic tests are expensive, their clinical role and overall benefit is not yet established, and it is not clear if they will be covered by insurance.
Prostate cancer is a malignant tumor that originates in the prostate gland. As with any cancer, if it advances or is left untreated in early stages, it may eventually spread through the blood and lymph fluid to other organs. Fortunately, prostate cancers tend to be slow growing compared to other cancers. Most older men eventually develop at least microscopic evidence of prostate cancer, but it often grows so slowly that many men with prostate cancer "die with it, rather than from it."
Description of the Prostate Gland
The prostate is a walnut-shaped gland located below the bladder and in front of the rectum. It wraps around the urethra (the tube that carries urine through the penis). The central area of the prostate that wraps around the urethra is called the transition zone. The entire prostate gland is surrounded by a dense, fibrous capsule.
Functions of the Prostate Gland
The prostate gland provides the following functions:
Changes During the Lifespan
The prostate gland undergoes many changes during the course of a man's life. At birth, the prostate is about the size of a pea. It grows only slightly until puberty, when it begins to enlarge rapidly, attaining normal adult size and shape, about that of a walnut, when a man reaches his early 20s. The gland generally remains stable until men reach their mid-40s, when, in most men, the prostate begins to enlarge again through a process of cell multiplication.
The major risk factors for prostate cancer are age, family history, and ethnicity.
Prostate cancer occurs almost exclusively in men over age 40 and most often after age 50. The average age at diagnosis is about 67. By age 70, about two-thirds of men have at least microscopic evidence of prostate cancer. Fortunately, the cancer is usually very slow growing, and older men with the cancer typically die of something else, often without even knowing they have prostate cancer.
Heredity plays a role in some types of prostate cancers. Men with a family history of the disease have a higher risk of developing prostate cancer. Having one family member with prostate cancer doubles a man's own risk, and having three family members increases risk by 11-fold. A specific gene, named HPC1 (for “hereditary prostate cancer”) was the first of several genes linked to inherited types of the disease.
Scientists are researching other genetic variations that may increase prostate cancer risk.
African-American men have higher rates of prostate cancer than men of other races. They are also more likely to develop prostate cancer at a younger age and to have more aggressive forms of the disease. However, race alone does not fully explain this difference. Prostate cancer is more common in North America and northern Europe and less common in Africa, Latin America, and Asia. Diet and other factors may play a role. For example, Asians who live in the United States have a higher rate of prostate cancer than those who live in Asia.
Male hormones (androgens), particularly testosterone, may play a role in the development or aggressiveness of prostate cancer. Other types of hormones, such as the growth hormone insulin-like growth factor-1 (IGF-1), may also be associated with some types of prostate cancer.
Prostatitis (inflammation of the prostate gland) may possibly be associated with increased prostate cancer risk. There may also be a possible relationship between prostate cancer and sexually transmitted infections, such as herpes virus and human papillomavirus, but no definite association has yet been proven.
Because a Western lifestyle is associated with prostate cancer, dietary factors have been intensively studied. Results have been inconsistent and inconclusive, however.
Fats. Some studies have found an association between high fat intake and prostate cancer. In particular, high consumption of red meat and high-fat dairy products has been linked to increased risk for prostate cancer. In contrast, the omega-3 fats found in certain fish (salmon, sardines, fresh tuna) may possibly be protective.
Vegetables and Fruits. A diet rich in vegetables, fruits, and legumes appears to protect against prostate cancer. However, it is not clear whether this is due to the nutrients contained in these foods, or the fact that these foods are low in fat. No specific vegetable or fruit has been proven to decrease risk. Lycopene, which is found in tomatoes, has been a target of research interest, but the evidence for its protective benefit is still inconclusive.
Vitamins and Minerals. Major clinical studies have found that vitamin and mineral supplements (vitamin E, vitamin C, vitamin D, and selenium) do not prevent prostate cancer. (Researchers studying whether high doses [400 IU daily] of vitamin E supplements could reduce the risk of prostate cancer found that they had the opposite effect and actually increased risk.) Nutritious foods that are part of a healthy diet are the best sources for vitamins and minerals. A high intake of calcium has been linked to an increased risk of prostate cancer in some studies.
The below factors may help reduce the risk of developing prostate cancer.
Diet. Eat a healthy diet rich in fruits, vegetables, and legumes (beans). Limit consumption of red meat and high-fat dairy products. There is some evidence that a low-fat diet may help protect against prostate cancer.
Weight and Exercise. Maintain a healthy weight through diet and regular physical activity.
5-ARIs (Controversial). If you’re at higher-than-average risk for prostate cancer, you may wish to discuss with your doctor whether 5-ARI medications may help lower your risk. The 5-ARI drugs finasteride (Proscar, generic) and dutasteride (Avodart) are prescribed to help improve urinary symptoms associated with benign prostatic hyperplasia (BPH ). Studies have suggested that 5-ARIs lower a man’s overall risk for developing prostate cancer. However, based on these studies, the FDA revised these drugs’ prescribing labels to indicate that 5-ARIs may also increase the risk for being diagnosed with high-grade aggressive types of prostate cancer. A 2013 study reported that 5-ARI therapy neither increases nor decreases the risk of death from prostate cancer. The 5-ARIs are not approved for prostate cancer prevention and their use for this purpose is controversial.
Prostate cancer is the most common internal cancer in American men. (For men, skin cancer is the most common cancer, and only lung cancer causes more cancer deaths.) About 1 in 6 men will be diagnosed with prostate cancer over the course of their life. But because so many prostate tumors are low-grade and slow growing, and men are usually older when they are diagnosed with it, most men diagnosed with prostate cancer eventually die of something else.
At the time of diagnosis, most men have localized prostate cancer (cancer confined to the prostate gland). The prognosis for men with localized prostate cancer is excellent. Nearly 100% of men with localized prostate cancer live at least 5 years after diagnosis. The same is true for men with regional prostate cancer, which means the cancer has spread from the prostate gland to nearby areas in the body.
Only about 5% of men are diagnosed with advanced or distant cancer that has spread throughout the body. For these men, the 5-year relative survival rate is 29%.
A survival rate indicates the percentage of patients who live a specific number of years after the cancer is diagnosed. A relative survival rate compares the survival of people with a specific type of cancer to the expected survival of people who do not have cancer and will die from other causes.
Overall, for prostate cancer, the 10-year relative survival rate is about 98% and the 15-year survival rate is about 91%. After 15 years, survival rates stabilize.
The odds of survival depend in part on how far advanced the cancer is when a man is first diagnosed. Men who are diagnosed with low-grade prostate cancers have a minimal risk of dying from prostate cancer for up to 20 years after diagnosis. However, men diagnosed with more aggressive forms of prostate cancer have a higher risk of dying within 10 years.
If cancer recurs after initial treatment for early-stage tumors, it is still potentially curable if it is contained within the prostate, although in most cases the cancer has spread. Hormone treatments for such recurring cancers can often prolong survival for years, although the cancer almost always returns again.
Prostate cancer usually causes no symptoms in the early stages. As the malignancy spreads, it may constrict the urethra and cause urinary problems.
Later-stage urinary symptoms may include:
Although advanced prostate cancer can cause these symptoms, they are more commonly caused by benign prostatic hyperplasia and other non-cancerous conditions.
Significant pain in one or more bones may indicate the occurrence of metastases (spreading of cancer). This chronic pain occurs most often in the spine and sometimes flares in the pelvis, the lower back, the hips, or the bones of the upper legs. It may be accompanied by significant unexplained weight loss and fatigue.
Benign Prostatic Hyperplasia (BPH). BPH is a urinary condition that can develop into an enlarged prostate, which puts pressure on the urethra and causes urinary problems. BPH is not a cancerous or precancerous condition, but its symptoms can mimic late-stage prostate cancer.
Prostatitis. Prostatitis is an inflammation of the prostate, often caused by bacterial infections. Symptoms include urgency, frequency, and pain in urination, sometimes accompanied by fever or blood in the urine.
The goal of screening is to find cancer at an early stage before it has caused symptoms. To be considered successful, a screening test should lead to treatments that prolong life or reduce discomfort and improve the quality of life.
Two standard screening tests are used for early detection of prostate cancer:
There is great uncertainty and controversy over whether the benefits of regular screening for prostate cancer outweigh the risks for most men. Prostate cancer is very common, especially among older men, and is usually slow growing. Doctors cannot yet predict accurately which early-stage tumors pose a risk of being aggressive and need treatment, and which tumors should be left alone. The concern is that routine screening for early detection of tumors may lead to invasive and unnecessary treatment. The consensus is that the test is not helpful for asymptomatic men who are at average risk for prostate cancer.
The controversy over prostate cancer screening centers on the use of the PSA test as a screening tool. The test is not accurate enough to either rule out or confirm the presence of cancer. Although PSA levels are often elevated in men with prostate cancer, some men with prostate cancer have normal PSA results. In addition, PSA levels can be increased by various factors other than prostate cancer, including benign prostatic hyperplasia, prostatitis, advanced age, and ejaculation within 48 hours of the test.
The main concern is that PSA screening may result in the detection of some cancers that would never have bothered the patient and would never have posed a threat to his life. Older men are less likely to die from prostate cancer than from heart disease and other problems. Relying too much on the test may lead to unnecessary biopsies and potentially harmful treatments. Several major studies have found that PSA screening saves few if any lives. The United States Preventive Services Task Force (USPSTF) currently recommends against PSA-based screening for prostate cancer.
The American Cancer Society (ACS) recommends that starting at age 50, men should discuss with their doctors the pros and cons of having a PSA test with or without a digital rectal exam. Men who are at higher-than-average risk for prostate cancer (including those with a family history of prostate cancer and all African-Americans) should initiate this talk at age 40 - 45. When and how often a man should be retested depends on his PSA level. The American Urological Association (AUS) recommends the test primarily for men ages 55 – 69 years, after a similar discussion of risks and benefits, with retesting every 2 years..
Biopsy. If cancer is suspected, the doctor will order a biopsy. Only a biopsy, in which a tiny sample of prostate tissue is surgically removed, can actually confirm a diagnosis of prostate cancer. A biopsy is usually performed to confirm or rule out cancer based on a combination of PSA test levels, findings on the DRE, family history, and patient’s age and ethnicity. If a biopsy gives a negative result but the doctor still suspects cancer, repeat biopsies may be performed.
An ultrasound procedure called transrectal ultrasonography (TRUS) may be used to help the doctor see where to take the needle biopsy. Ultrasound is not effective as a diagnostic tool by itself because it cannot differentiate very well between benign inflammations and cancer.
PSA Levels and Velocity. Once cancer is diagnosed, PSA levels may help to determine its extent. If PSA levels are lower than 20 ng/mL, it is likely that the cancer has not spread to distant sites. PSA levels over 40 ng/mL are a strong indicator that cancer has metastasized (spread elsewhere in the body). PSA levels are also monitored after treatments begin. Changes in the level can show if a treatment is working or if the cancer has come back.
Doctors also monitor how quickly PSA levels rise over time. This rate is called PSA velocity (PSAV). The PSAV may help determine when treatment should begin and which treatment should be used. A high rate of PSAV is considered to be 2 ng/mL a year. Research suggests that men with early-stage prostate cancer who have a slow PSAV are more likely to live longer than men with rapidly rising PSA levels.
Test for Metastasis. If the biopsy indicates cancer, and the PSA is above 20 ng/mL, the doctor will order other tests to determine whether or how far the cancer has spread:
Genetic Tests. Scientists are developing several new genetic tests, including the Oncotype DX Prostate Cancer Test, that may help predict if a cancer is low-risk or if it could become aggressive (fast-growing). Genetic tests measure the gene activity in prostate tissue tumor samples and can help predict whether the cancer will grow and spread. Tests like these may help doctors determine whether or not a man with prostate cancer needs treatment, and could potentially spare low-risk patients from treatments that may do more harm than good. Genetic tests are expensive, their clinical use and overall benefit has not yet been established, and it is still unclear if they will be covered by insurance.
Grading refers to how abnormal the cells look under a microscope and how likely the cancer is to advance and spread. A pathologist will read the biopsy report and assign a grade to the tumor cells using the Gleason system of scoring.
Staging refers to the extent the cancer has spread. Based on the grade, TNM staging system, PSA test result, digital rectal exam, and possibly imaging tests, the doctor stages the cancer. The overall stage of cancer can help the doctor determine treatment options.
Gleason Grade. The Gleason system grades tumors on a scale of 1 - 5 based on how well or poorly differentiated the cancer cells look under a microscope. Grade 1 means that the cells resemble normal prostate tissue. Grade 5 means that the cells look very abnormal and are poorly organized throughout the prostate. Grades 2 - 4 fall in between with cells showing increasingly irregular features.
Gleason Score. Most prostate cancers contain a mix of tumor grades. To determine a Gleason score, two numbers are assigned, representing the dominant grade and then the minor grade. The cancer is then "scored" by adding the dominant grade plus the minor grade. For example, a tumor with a dominant grade of 3, and a minor grade of 4 is given a Gleason score of 7.
Gleason scores range from 2 - 10. A higher score means that the cancer cells look very different from normal cells. A higher score also means that it is more likely that the tumor will spread aggressively. In general, Gleason scores indicate:
A tumor's stage is an indication of how far it has spread from its original site. Cancers are staged according to whether they are still localized (still within the prostate gland) or have spread beyond the original site. The current prostate cancer staging system is the TNM system.
The TNM system refers to clinical tumor stages as:
T followed by numbers 0 through 4 refers to the size and extent of the tumor itself.
Stage, T1 - T4
The tumor cannot be felt or seen using imaging techniques.
T1a. Cancer cells are incidentally found in 5% or less of tissue samples from prostate surgery unrelated to cancer.
T1b. Cancer cells found in more than 5% of samples.
T1c. Cancer cells identified by needle biopsy, which is performed because of high PSA levels.
The cancer is confined to the prostate but can be felt as a small well-defined nodule.
T2a. Tumors are in half a prostate lobe.
T2b. Tumors are in more than half a lobe.
T2c. Tumors in both lobes.
The tumor extends through the prostate capsule.
The tumor is fixed to or invades adjacent structures.
N followed by 0 through 3 refers to whether the cancer has reached the regional lymph nodes, which are located next to the prostate in the pelvic region.
Stage, N0 - N3
Regional lymph nodes are still cancer-free.
A small tumor is in a single pelvic node.
A medium-size tumor is in one node, or small tumors are in several nodes.
A large tumor is in one or more nodes.
M stages refer to metastasis (tumors developing outside the prostate).
Metastasis has not occurred (cancer has not spread beyond the regional lymph nodes).
Cancer has spread to lymph nodes beyond the regional lymph nodes.
Cancer has invaded the bones.
Cancer has spread to other sites.
The T, N, and M stages are used along with the grade, PSA test result, and other factors to determine the overall stage of the cancer:
[For more information on staging, see Treatment section of this report.]
Treatment choices are generally based on the patient's age, the stage and grade of the cancer, overall health status, and the patient's personal preferences for the risks and benefits of each therapy.
Patients should be aware that doctors may prefer a specific treatment depending on their specialty, with urologists and medical oncologists tending to recommend watchful waiting, surgery, or hormone therapy and radiation oncologists recommending radiation therapy. It is always wise to seek a second opinion. Delaying treatment, while having the cancer monitored for signs of progression, is also an acceptable option.
Depending on the cancer stage and other factors, patients have four main treatment options:
The U.S. National Cancer Institute recommends the following treatment options by cancer stage:
Overview of Treatment Options for Localized Prostate Cancer. To date, neither treatment nor active surveillance has emerged with a definitive survival advantage for localized prostate cancer. Some research suggests that treatment may provide a survival advantage over watchful waiting for some men with early-stage prostate cancer. The men who are most likely to benefit from active treatment include those younger than 65 with good general health and PSA levels above 10.
Recent guidelines recommend that patients with localized cancer should be classified as low, intermediate, or high risk. Doctors determine the risk category by using criteria such as PSA tests, tumor aggressiveness, and the clinical stage of the tumor. Based on these risk groups, evidence indicates that:
If prostate cancer has been by radical prostatectomy, PSA levels should drop to zero after surgery. After radiation, PSA levels do not drop as far because some of the prostate gland remains. A sudden rise or persistently elevated PSA levels after treatment are often indications that prostate cancer persists.
It is common for PSA levels to temporarily rise or "bounce" following radiation seed implantation without signaling cancer recurrence. Rising PSA levels do not necessarily mean that the cancer has spread or even that clinical cancer will recur during a man's lifetime.
Treatment options for recurrent cancer depend on various factors, including prior treatment, site of recurrence, coexistent illnesses, and individual patient considerations.
Prostate cancer treatments can cause distressing side effects including erectile dysfunction, urinary and bowel leakage (incontinence), and fatigue. A man must weigh his own emotional responses to the possibility of these side effects versus the possible stress of active surveillance.
Side effects vary among patients and it is difficult to predict how an individual patient will respond. In general, the side effects most likely to occur by treatment modality are:
Active surveillance involves lifestyle change and careful monitoring of cancer with conversion to active therapy if the disease progresses. With this approach, patients have a digital rectal exam and PSA blood test every 6 - 12 months. If test results indicate cancer progression, doctor and patient consider treatment options (surgery, radiation, or drugs). Patients should exercise and eat healthy foods. Patients should report symptoms such as weight loss, pain, urinary problems, fatigue, or erectile dysfunction to their doctors. Active surveillance was formerly called “watchful waiting.” Watchful waiting is now mostly associated with palliative measures for advanced cancer.
Active surveillance may be most appropriate for the following patients:
Some doctors think that because prostate cancer grows so slowly, it is likely that older men will die from causes unrelated to the cancer. There is therefore little potential benefit from surgery or radiation, with both posing a risk for erectile dysfunction and incontinence. The choice is a difficult one. It is important that patients find a doctor who can provide them with all the necessary information so that they can make an informed decision.
In men whose cancer is confined to the prostate, surgical resection (radical prostatectomy) offers the potential for cure. Most patients can consider themselves disease-free if their PSA levels remain undetectable 10 years after surgery.
Radical prostatectomy is the surgical removal of the entire prostate gland along with the seminal vesicles (the vessels that carry semen) and surrounding tissue. The surgeon may also remove the pelvic lymph nodes (a procedure called pelvic lymphadenectomy). The incision can be made in one of the following regions:
The gland and other structures are then removed. The operation lasts 2 - 4 hours.
Minimally Invasive Prostatectomy. Less invasive surgical techniques with laparoscopy use smaller incisions and allow faster recovery, but they require special surgical training. Laparoscopic surgery inserts an instrument with a small video camera attached to it to help guide the surgeon. Robotic-assisted laparoscopic radical prostatectomy involves the surgeon directing a robotic arm through a computer monitor. Not every hospital can do robotic-assisted laparoscopic prostatectomy, and these procedures are difficult to perform. Although robotic surgery is gaining popularity, it is not clear that it produces better results than traditional operations.
Nerve-Sparing Techniques. In retropubic open surgery, laparoscopic surgery, and robot-assisted surgery, the surgeon will attempt to spare the nerves that control erection:
Nerve-sparing techniques can improve quality of life, by decreasing the occurrence of incontinence and erectile dysfunction. In cases where the tumor lies too closely to the nerve, nerve-sparing techniques may not be possible.
Recuperation. Patients remain hospitalized for about 3 days after an open procedure or 2 days after less invasive procedure. Full recovery at home takes about 3 - 5 weeks. A temporary catheter used to pass urine is kept in place when the patient is sent home and is usually removed about 3 weeks after the open operation or 1 week after a minimally invasive procedure. In general, younger patients with early-stage cancers recover fastest and experience the fewest side effects.
The main complications from radical prostatectomy are urinary incontinence and erectile dysfunction. Other complications include the usual risks of any surgery, such as blood clots, heart problems, infection, and bleeding. Minimally invasive procedures usually result in less pain and a faster return to activity.
Urinary Incontinence. Urinary incontinence is a common complication. When the urinary catheter is first removed following surgery, nearly all patients lack control of urinary function and will leak urine for at least a few days and sometimes for months. Normal urinary function usually returns within about 18 months. A percentage of men will continue to have small amounts of leakage with heavier exertion or possibly sexual activity.
If incontinence persists beyond a year, patients may require drug therapy or surgery.
Erectile Dysfunction. Erectile dysfunction after radical prostatectomy is caused by nerves that were damaged or removed during the surgery. Virtually all men will have problems with erectile dysfunction after surgery. It can take up to 1 to 2 years to recover erectile function after surgery. Because seminal glands are removed along with the prostate gland during surgery, men who regain sexual function will not produce semen during orgasm (“dry ejaculation”).
With the use of nerve-sparing techniques, men below age 60 who were sexually active before surgery seem to have a better chance of returned sexual function. PDE5 inhibitor drugs such as sildenafil (Viagra), vardenafil (Levitra), tadalafil (Cialis), or avanafil (Stendra) may help some men regain erectile function. Other treatments for erectile dysfunction (alprostadil injections, vacuum devices, penile implants) may also be options.
Radiation therapy may be used as an initial treatment for localized prostate cancer. It may also be used as treatment for cancer that has not been fully removed or has recurred after surgery. In advanced cancer, radiation therapy is used to shrink the size of the tumor and relieve symptoms.
The two main radiation treatments for prostate cancer are:
In some cases, both techniques may be used to treat high-risk patients.
External beam radiation therapy (EBRT) uses a machine that focuses a beam of radiation directly on the tumor. An EBRT treatment lasts a few minutes and is given 5 times a week over the course of 7 - 9 weeks. Doctors use imaging techniques such as computed tomography (CT) and magnetic resonance imaging (MRI) to precisely map out where the beams are aimed at the tumor cells.
Newer types of EBRT allow doctors to increase radiation doses while minimizing damage to nearby tissue. Higher radiation doses may reduce the risk for cancer recurrence and improve survival outcome. Three-dimensional conformal radiation therapy (3D-CRT) uses a computerized program and three-dimensional image of the prostate to precisely target the tumor. Other techniques related to 3D-CRT include:
Fatigue is a common side effect for several months following radiation therapy. Other complications may include:
Gastrointestinal and Bowel Complications. Short-term effects include nausea and loss of appetite. Diarrhea is a very common side effect and can last for the duration of therapy. It is often treated with Lomotil. It usually goes away eventually, but some patients may have diarrhea flare-ups for years afterward. Newer 3D-CRT techniques may be less likely to cause diarrhea than standard EBRT.
Urinary Problems. Many patients experience a need for frequent urination shortly after radiation therapy, and urgency persists long-term for some patients. Some men experience urinary incontinence (loss of bladder control) but this is less common with radiation than with surgery.
Erectile Dysfunction. Unlike surgery, erectile dysfunction does not usually occur immediately following radiation therapy. However, the risk for this complication increases progressively over a year or more. Drug therapies for erectile dysfunction may help.
Brachytherapy is a type of radiation therapy used mainly for men who have early-stage or localized prostate cancer. It can also be used in combination with external beam radiation therapy.
Brachytherapy involves implanting radioactive pellets ("seeds") directly into the prostate. Implants can be permanent or temporary:
Side effects for brachytherapy are similar to those for external beam radiation therapy. Side effects specific to brachytherapy include:
Radiation may help select patients who still have detectable levels of PSA after surgery (generally 2 ng/mL or less). It may even be useful years after surgery if PSA levels rise.
Depending on timing, radiation after treatment failure is referred to as either:
Cryosurgery is an alternative to standard prostatectomy for men with early-stage, localized prostate cancer who do not want or who are not appropriate candidates for radical prostatectomy. It is also an alternative to radiation therapy.
The goal of cryosurgery is destruction of the entire prostate gland and possibly surrounding tissue. Steel probes are inserted through the skin between the anus and the rectum and guided into the prostate using transrectal ultrasound. Liquid nitrogen is pumped through the probes to freeze all prostate cells, both healthy and cancerous. For success, cryosurgery requires a uniformly frozen area. The dead cells are absorbed and eliminated by the body.
Cryosurgery is typically a 2-hour outpatient procedure, although some patients may need to stay in the hospital overnight. Cryosurgery may also be used as a salvage procedure for patients who have undergone radiation therapy and have had cancer recurrence detected early. It is generally not helpful for men with very large prostate glands.
Nearly all patients experience erectile dysfunction after cryosurgery, and urinary incontinence is also common in men who were first treated with radiation therapy. Other complications of cryosurgery include urinary retention, swelling, and fistula formation. Incontinence and fistulas are more likely to occur when cryosurgery is used as a salvage procedure than when it is used as a primary procedure.
This therapy is still considered experimental by some doctors, and there are no long-term data to compare its effectiveness with standard prostatectomy. For this reason, cryosurgery is generally not considered as a first-line initial treatment.
Androgen deprivation therapy (also called androgen suppression therapy or hormone therapy) uses treatments to reduce levels of male hormones such as testosterone, which stimulate the growth of prostate cells. Androgen deprivation therapy suppresses or blocks testosterone by either:
Androgen deprivation therapy is not usually recommended as a first-line therapy for early-stage prostate cancer. It is mainly used for:
Androgen deprivation therapy may also be used:
Bilateral orchiectomy is the surgical removal of both testicles (surgical castration). It is the single most effective method of reducing androgen hormones but its effects are permanent. Orchiectomy plus radical prostatectomy may delay progression in patients with cancers that have spread only to the pelvic lymph nodes.
Men who have orchiectomy have reduced sexual function and desire. Patients do not experience a reversal of sex characteristics and the voice does not change. Like all androgen deprivation therapies, orchiectomy increases the risk for osteoporosis.
LH-RH Agonists and Antagonists. The main drugs used for suppressing androgens are called luteinizing hormone-releasing hormones (LH-RH) agonists. They are also known as gonadotropin-releasing hormone (GnRH) agonists or LH-RH analogs. These drugs block the pituitary gland from producing hormones that stimulate testosterone production.
LH-RH agonists include leuprolide (Lupron, Eligard, Viadur, generic), goserelin (Zoladex),triptorelin (Trelstar), and histrelin (Vantas). These drugs are given as injections or as implants placed under the skin. LH-RH agonists produce a testosterone surge (“flare”) in the first week, which may intensify symptoms including bone pain if the cancer has spread to the bones. After this phase, testosterone levels drop to near zero. LHRH agonists can also cause PSA levels to rise temporarily.
LH-RH antagonists work similarly to LH-RH agonists but do not cause a testosterone surge. The FDA has approved one LH-RH antagonist drug, degarelix (Firmagon), for treatment of advanced prostate cancer. It is given as a monthly injection.
Common side effects of these drugs include hot flashes, fatigue, testicle shrinkage, and breast enlargement. These drugs may increase blood sugar levels and the risk for developing diabetes. They may also increase risk for heart attack, stroke, and sudden death.
Anti-Androgens. Anti-androgens are drugs used to block the effects of testosterone. Anti-androgens are not typically used by themselves. They are usually added when another hormone therapy stops working. They are generally used in combination with LH-RH agonists. This type of treatment is called combined androgen blockade.
The anti-androgen drugs used for prostate cancer treatment are flutamide (Eulexin, generic), nilutamide (Nilandron), and bicalutamide (Casodex, generic). They are taken as daily pills. When taken with an LH-RH agonist, hot flashes and breast tenderness is intensified. Nilutamide can cause problems seeing in the dark.
Side Effects. All types of hormone drug therapy can help delay cancer growth but this treatment can cause significant side effects including:
In addition, there is growing evidence that androgen deprivation drug therapy increases the risks for heart attack, stroke, and diabetes. These drugs increase body weight, which can lead to decreased insulin sensitivity and harmful changes in cholesterol levels.
Guidelines recommend that men who receive androgen deprivation therapy should have regular follow-up exams with their primary care doctors within 3 - 6 months after starting therapy. The doctor should monitor the patient’s blood pressure and perform blood sugar (glucose) and cholesterol (lipid tests) at least once a year.
Continuous Versus Intermittent Therapy. When prescribing hormone therapy drugs, some doctors recommend periodically stopping and restarting treatment (intermittent therapy). This approach appears to help reduce erectile dysfunction, hot flashes, and other hormone therapy side effects that impair quality of life. However, it is not clear if intermittent therapy works as well as continuous therapy for prostate cancer treatment. Some studies indicate that continuous therapy is more effective or that intermittent therapy should only be used for select types of prostate cancer. Other research suggests that intermittent androgen deprivation is as effective as continuous therapy. More research is needed.
Hormone therapy is initially very effective, but after several years the cancer usually starts growing again. Prostate cancer that no longer responds to hormonal treatment is called castration-resistant. (It was formerly called hormone-resistant or hormone-refractory cancer.) When castration-resistant prostate cancer advances and spreads throughout the body it is called metastatic castration-resistant prostate cancer (mCRPC). There are several treatment options, including new types of drugs. Most of these therapies prolong survival by a few months.
Chemotherapy. Chemotherapy drugs for advanced prostate cancer include docetaxel (Taxotere), mitoxantrone (Novantrone, generic), estramustine (Emcyt), and various platinum-based drugs, such as carboplatin. These drugs are often combined with other cancer drugs (such as 5-fluorouacil) or corticosteroids (such as prednisone). The main chemotherapy treatment combines docetaxel with prednisone. Cabazitaxel (Jevtana) is a newer chemotherapy drug approved for patients whose condition has worsened during or after treatment with docetaxel. It is also used in combination with prednisone.
Chemotherapy regimens may help extend survival time by several months. Side effects can be serious and may include gastrointestinal problems (nausea, vomiting, or diarrhea), fatigue, low blood cell counts, and increased risk for blood clots.
Abiraterone (Zytiga). Abiraterone (Zytiga) is an anti-androgen drug that is used for patients with metastatic castration-resistant prostate cancer who have already been treated with docetaxel. It is taken once a day as a pill along with prednisone. Abiraterone is also approved for use for metastatic cancer prior to chemotherapy. Side effects may include joint swelling, fluid build-up in legs and feet, muscle discomfort, hot flashes, high blood pressure, and low levels of potassium in the blood.
Enzalutamide (Xtandi). Enzalutamide (Xtandi) is another new anti-androgen for men with advanced prostate cancer who were previously treated with docetaxel. Enzalutamide is taken as a daily pill. Unlike abiraterone, it does not need to be taken along with prednisone. Its side effects are similar to abiraterone except that enzalutamide may increase the risk for seizures. .
Sipuleucel-T (Provenge). In 2010, the FDA approved a new type of treatment for select men with advanced prostate cancer. Sipuleucel-T (Provenge) is a cancer “vaccine.” Unlike typical vaccines, it does not prevent disease. Instead, it uses the patient’s own immune system to fight the cancer. Each vaccine is individually manufactured by obtaining a patient’s immune cells from his blood. The cells are then exposed to a special type of protein and infused back into the patient.
In clinical trials, Provenge extended survival time by an average of 4 months. Side effects ranged from mild (chills, fatigue, fever, nausea, joint and muscle aches) to severe (stroke). Provenge is very expensive (about $93,000 a year), but some insurers, including Medicare, are beginning to offer coverage for it, with some restrictions.
Radium-223 (Xofigo). In 2013, the FDA approved radium-223 injection (Xofigo) for treatment of metastatic castration-resistant prostate cancer that has spread to the bones but not other organs. Xofigo is a radioactive medicine that binds to the mineral in bones. It targets and delivers radiation directly to bone tumors without damaging surrounding healthy tissue. In clinical trials, men treated with Xofigo lived about 3 months longer than those who did not receive the drug. This medication costs about $70,000 for six injections.
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