Microsoft word - prostate cancer manual2 _3_.doc

Prostate Cancer 2005
Assistant Professor, University of Colorado Terms, Definitions, and Additional Information About
Prostate Cancer
Prostate Cancer Terms and Definitions
Index To Prostate Cancer Terms and Definitions:
Adjuvant
Age-Specific PSA
Androgen
Androgen Deprivation
Anti-Androgen
Benign
Benign Prostatic Hypertrophy
Bicalutamide (Cassodex)
Biopsy
Bisphosphonates
Bladder
Bone Scan
Brachytherapy
Capsule
Carotenoid
Catheter
Clinical Trial
Complexed PSA
Computerized Tomography
Cryotherapy
Deltanoids
Definitive Treatment
Digital Rectal Exam
Dihydrotestosterone (DHT)
Distal
Downstaging
Dutasteride (Avodart)
Ercetile Dysfunction
External Sphincter
Extracapsular
False Negative
False Positive
Finasteride (Proscar)
Fistula
Flavinoid
Flutamide (Eulixin)
Free PSA
Goserelin (Zoladex)
Grade
Histology
Hormones
Impotence (Erectile Dysfunction)
Incidence
Incontinence
Internal Sphincter
Isoflavones
Kegel Exercises
Laparoscopic
Leutinizing Hormone Releasing Hormone (LHRH) Agonist
Leutinizing Hormone Releasing Hormone (LHRH) Antagonist
Localized
Luprolide (Lupron)
Lycopene
Malignancy
Malignant
Margin
Metastases
Metastasize
Monotherapy
Nadir
Neo-Adjuvant (therapy)
Palliative Care
Palpate
Pathology
Perineum
Placebo
Posterior
Prevelance
Pro-PSA
Prognosis
Prospective Trial
Prostate
Prostate Specific Antigen (PSA)
Prostatectomy
Prostatic Intraepithelial Neoplasia (PIN)
Proximal
PSA Velocity
Screening
Selenium
Semen
Seminal Vesicles
Sensativity
Serum
Specificity
Sperm
Sphincter
Spinal Cord Compression
Stage
Systemic
Ureter
Urethra
Vas Deferens
Vertebra

Information About Prostate Cancer
Index to Information About Prostate Cancer:
Prostate Cancer Prevention
Screening for Prostate Cancer
Staging Prostate Cancer and Predicting Prognosis
Surgery and Prostate Cancer
Radiation and Prostate Cancer
Cryotherapy and Prostate Cancer
Hormones (Androgen Deprivation), Bisphosphonates, and Prostate Cancer
Androgen Independent Prostate Cancer and Clinical Trials
References
Terms and Definitions
Adjuvant: Concurrent or additive, generally a reference to treatments
given at the same time

Age-Specific PSA: The adjustment for PSA for age in the hopes to
improve its sensitivity and specificity. By lowering the threshold of
PSA for younger men, it is hoped that fewer prostate cancers will be
missed, while increasing the threshold for older men, it is hoped that
fewer unnecessary biopsies for enlarged prostate conditions without
cancer will be performed

Androgen: A term for the male hormone testosterone

Androgen Deprivation: The act of removing or decreasing
circulating testosterone (which stimulates prostate cancer growth)
with medications or surgery in the hopes of slowing the growth of
prostate cancer

Androgen Independent Prostate Cancer: Prostate cancer that
appears to be progressing despite treatment with androgen
deprivation
Anti-Androgen: A medication, usually given in tablet form, which
blocks the effect of circulating testosterone. Examples of this
medication include Flutamide and Bicalutamide (or Cassodex)

Benign: Non-cancerous

Benign Prostatic Hypertrophy: The non-cancerous growth seen in
most men’s prostate over time. This growth typically occurs in the
central zone of the prostate (where the urine flows during elimination)
and may result in urinary symptoms such as a slow stream, voiding
frequently, incomplete emptying, and difficulty initiating the urinary
stream

Bicalutamide (Cassodex): An anti-androgen given in combination
with Leutinizing Hormone Releasing Hormone (LHRH) agonsists at
the initiation of treatment of advanced prostate cancer. Some
practitioners continue this medication even after the first two weeks.
Rarely, the medication is used without the injectable LHRH agonist

Biopsy: The sampling of tissue, usually performed to evaluate for
cancer
Bisphosphonates: Medications given orally or intravenously that
have been shown to stop the destruction of bone. These are
generally given for patients with osteoporosis and have been found to
decrease fracture rates in patients with bone metastases
Bladder: A hollow muscular pelvic organ which stores and expels
urine
Bone Scan: A radionucleotide scan whereby antibodies that detect
rapid calcium turn over are linked to radioactive signals so that areas
of possible bone metastases can be identified

Brachytherapy: A treatment for low-risk prostate cancer that
involves the surgical placement of small radioactive seeds which
slowly release radiation to the surrounding prostate tissue. The two
main types of seeds used to treat prostate cancer are those made of
radioactive Iodine and or Paladium.

Capsule: A very thin layer of tissue surrounding an organ

Carotenoid: Antioxidant substance found in tomatoes, guava,
rosehip, watermelon and pink grapefruit. This substance helps give a
red color to these fruits and vegetables and may be useful in prostate
cancer prevention and treatment
Catheter: Latex or silastic tube allowing for the passage of a fluid,
generally referring to a narrow tube which facilitates urinary drainage
via the urethra
Clinical Trial: An investigation into a novel surgical, medical, or
other disease treatment that involves treatments that are at least as
good as the standard-of-care for that disease. The most meaningful
clinical trials are randomized, wherein patients are randomly assigned
to treatment options. Some clinical trials are also “blinded” (where
the patient and/or the physician are not notified of which treatment
arm the patient is involved in)

Complexed PSA: PSA protein that is bound to specific proteins that
circulate in the blood. The percentage of complexed PSA compared
to total PSA may be a more specific indicator of prostate cancer than
total PSA

Computerized Tomograpy (CT): A two-dementional x-ray which
shows anatomic detail of soft tissue structures and can be used to
evaluate for the spread of prostate cancer

Cryotherapy: The treatment of prostate cancer accomplished by
placing probes through the skin, into the prostate to freeze the
cancerous tissue. This can be used as a first-line treatment or in
cases where previous radiation treatments have not been effective.
This treatment is associated with a relatively high rate of erectile
dysfunction

Deltanoids: Vitamin D analogs that may be useful in the prevention
or treatment of prostate cancer
Definitive Treatment: A treatment recommended with an intent to
cure. Definitive treatments for prostate cancer include surgery,
radiation, and cryotherapy.
Digital Rectal Exam: The process of examining the prostate. A
clinician’s finger is inserted into the patients rectum whereby the back
side of the patient’s prostate can be felt. Nodules or lumps of the
prostate can be a sign of prostate cancer, prostatic stones, or areas
of asymmetric prostate cancer growth. A special reagent can also be
used for check for blood in the gastrointestinal tract as part of the
digital rectal exam

Dihydrotestosterone (DHT): A hormone made from testosterone
which performs the same functions, but is considerably more potent
than testosterone itself
Distal: Further from the center of the body

Downstaging: The process by which a detected cancer is made to
be less extensive over time. This is usually accomplished by either
by screening or prevention

Dutasteride (Avodart): A 5-alpha-reductase inhibitor that
preventions the formation of dihydrotestosterone (DHT) from
testosterone. This medication can be used to shrink the prostate and
a similar medication has been used in experimental studies to
prevent or treat prostate cancer

Erectile Dysyfunction: The inability to produce or maintain an
errection suitable for sexual penetration
External Sphincer: A voluntary muscle just below the prostate that
eventually provides urinary control in men who have had their
prostates removed. Women rely only on the external sphincter for
urinary control.

Extracapsular: Disease that has spread beyond the capsule of the
primary affected organ

False Negative: A negative test result in a patient who actually
harbors the condition being evaluated
False Positive: A positive test in a patient who does not harbor the
condition evaluated for by the test

Finasteride (Proscar): A 5-alpha-reductase inhibitor that preventions
the formation of dihydrotestosterone (DHT) from testosterone. This
medication can be used to shrink the prostate and has been used in
experimental studies to prevent or treat prostate cancer

Fistula: An abnormal connection between two organs or an organ
and the skin
Flavinoid: A naturally-occurring compound found in plant-based
foods which appears to act as an antioxidant. Flavonoids are found
in a variety of foods and beverages, including soy, cranberries,
peanuts, apples, chocolate, tea and red wine
Flutamide (Eulixin): An anti-androgen given in combination with
Leutinizing Hormone Releasing Hormone (LHRH) agonsists at the
initiation of treatment of advanced prostate cancer. Some
practitioners continue this medication even after the first two weeks.
Rarely, the medication is used without the injectable LHRH agonist

Free PSA: Circulating PSA which is unbound to serum proteins. In
general, the lower the percent free PSA value, the higher the risk of
prostate cancer being detected

Goserelin (Zoladex): An injectable LHRH agonist used to decrease
PSA and the growth of prostate cancer. Side effects of LHRH
agonsists include hot flashes, fatigue, occasional mental complaints
and osteoporosis over time

Grade: Gleason sum assigned to a particular tumor reflecting the
pattern visualized under the microscope by the pathologist which
predicts tumor behavior. Gleason sum is a compilation of two
numbers. Each number (1-5 scale) represents how typical (1) or
aggressive (5) a tumor looks under the microscope. The sum is of
the two scores suggests the overall prognosis. A Gleason’s sum of
2-6 represents cancers are considered low-grade and tend to behave
very well (sometimes even without treatment), Gleason’s sum 7
cancers are considered to be intermediate-grade and behave in a
more aggressive fashion. Gleason sum 7 cancers are more likely to
recur after definitive treatment and are more likely to spread or
metastasize. Gleason’s sum 8-10 cancers are considered high-grade
or aggressive and are likely to recur after definitive treatment and are
more likely to spread or metastasize

Histology: The evaluation of tissue under a microscope
“Hormones”: A shorthand form of referring to androgen deprivation
or the act of significantly decreasing circulating testosterone in the
hopes of slowing the growth of prostate cancer
Impotence (erectile dysfunction): The inability to produce or
maintain an errection suitable for sexual penetration

Incidence: The rate of new development of a particular disease over
a particular period in time
Incontinence: The leakage of urine. In 15-20% of males who have
undergone prostate removal, “stress incontinence” can be identified.
Stress incontinence implies leakage with increased abdominal
pressure (such as when lifting a heavy object or coughing), but rarely
results in significant leakage amounts after prostatectomy

Internal Sphincer: An involuntary muscle located inside the central
prostate that provides excellent urinary control in men with the
prostate in tact. This muscle must be removed with prostatecotmy
Isoflavones: A group of compounds found in soy and other foods
being evaluated in the prevention and treatment of prostate cancer
Kegel Exercizes: Contractions of the external sphincter muscle to
improve urinary control

Laparoscopic: An approach to surgery that involves the use of tiny
instruments on long handles to minimize external scars

Leutinizing Hormone Releasing Hormone (LHRH) Agonist: A
medication given as an injection which suppresses testosterone in
the hopes of slowing prostate cancer growth. Examples of LHRH
agonists include Luprolide (Lupron/Eligard/Viadur) and Goserelin
(Zoladex). LHRH agonists should always be started with a
concurrent 2-4 week treatment with an oral anti-androgen
Leutinizing Hormone Releasing Hormone (LHRH) Antagonist: A
new medication also given as a slow-release injection which
decrases circulating testosterone, thereby decreasing PSA and
possibly prostate cancer growth. Unlike LHRH agonists, his
medication does not need to be taken with an oral anti-androgen
upon treatment initiation

Localized: Confined to one area of the body

Luprolide (Lupron): An injectable LHRH agonist used to decrease
PSA and the growth of prostate cancer. Side effects of LHRH
agonsists include hot flashes, fatigue, occasional mental complaints
and osteoporosis over time
Lycopene: An anti-oxidant occurring in reaonalbe levels in
processed red tomatoes that may have a role in the prevention and
treatment of prostate cancer; a type of carotenoid

Maligancy: Cancer
Malignant: Cancerous

Margin: The edge of the specimen that is removed surgically. In
prostate cancer, when a positive margin is identified there is a 40%
chance that a patient will have a rise in his PSA following surgery
when a positive margin is detected. This rate is less in patients who
have only one area of positivity

Metastases: Areas of cancer detected outside of the primary
cancerous organ. Surrounding lymph nodes and bones are common
areas for prostate cancer metastases

Metastasize: The act of a primary tumor spreading to other organ
systems

Monotherapy: A treatment given alone such as an anti-androgen
medication given alone without other pharmacologic, surgical, or
radiologic combination treatments
Nadir: The lowest point; generally used when referring to the lowest
PSA value detected following radiation in prostate cancer

Neo-Adjuvant (therapy): A therapy given before the primary therapy
(generally in the hopes of improving outcome)

Palliative Care: Palliative treatment or care given without the hope
for cure, but with the intent of improving the quality of life in a patient
with incurable disease
Palpate: To feel with one’s hands

Pathology: The microscopic evaluation of an abnormal tissue under
a microscope
Perineum: The anatomic location between the scrotum and anus

Placebo: A treatment (generally used in a study) that has no
activeingredients. Placebos are used to help produce a more
accurate assessment of how well the actual treatment is working
Posterior: The back side of an object, behind
Prevalence: The rate of the development of a disease over a given
period of time relative to the population at risk for development of the
disease

Pro-PSA: A PSA precursor that may be a more specific indicator of
prostate cancer than total PSA

Prognosis: Expected outcome from a given condition

Prospective Trial: A trial that is designed prior to initiation of the
study

Prostate: A gland that is used in sexual reproduction. The prostate
provides over 90% of the fluid content of male semen and assists
sperm in reaching the fallopian tube and egg

Prostate Specific Antigen (PSA): A protein made by the prostate
that can correlate with the presence of prostate cancer. PSA is made
in the prostate and increases with prostate growth, prostate cancer,
and prostate irritation

Prostatectomy: The process of removing the prostate and attached
seminal vesicles from its attachments to the bladder, urethra, and vas
deferens and reconnecting the bladder to the urethra

Prostatic Intraepithelial Neoplasia (PIN): Microscopic diagnosis
that may be an indicator of prostate cancer elsewhere in the prostate
or may be a precursor to the development of prostate cancer. Most
clinicians recommend a repeat prostate biopsy when PIN is detected
on initial biopsy, as the rate of finding cancer on repeat biopsy is as
high as 50%
Proximal: Closer to the body’s center

PSA Velocity: The change in PSA over time. A PSA velocity of less
than 0.75ng/ml per year is much less concerning than a velocity of
0.75ng/ml per year or greater
Screening: The process of attempting to find a disease prior to its
symptomatic manifestation in the hopes of improving disease
outcomes

Selenium: A trace mineral that may be helpful in stimulating the
formation of antioxidants which are helpful in prostate cancer
prevention. Animals that eat grains or plants that are grown in
selenium-rich soil have higher levels of selenium in their muscle.
Grains are also a source of selenium and Brazil nuts are known to be
an excellent source of the mineral
Semen: Ejaculatory fluid made up of prostatic secretions (90%) as
well a sperm (10%)

Seminal Vesicles: Fluid-filled sacks on the back surface of the
prostate that contribute additional fluid to the ejaculate. Invasion of
prostate cancer into these structures suggests a higher stage of
disease and may portent a worse prognosis

Sensitivity: The ability of a screening test to detect disease if it is
present. Tests with high sensitivity have a low false negative rates
Serum: Liquid portion of blood
Specificity: The ability of a positive test to accurately diagnose
disease. Tests with high specificities have a low false positive rates
Sperm: Very tiny cells with a propulsory tail containing genetic
information. Sperm establish a full set of genetic information when
combined with an egg

Sphincter: A circumferential muscle. In the urethra, the sphincter(s)
control urinary flow. In the male, one sphincter is internal or inside
the prostate and does not require voluntary control the other is
outside the prostate and requires some voluntary signaling for
control, but can get stronger over time

Spinal Cord Compression: The collapse of the verterbral bones
resulting in pressure on the spinal cord. Neurological symptoms such
as paralysis, inability to empty one’s urine or bowel contents can be
the result of spinal cord compression. This condition is increased
with vertebral metastases
Stage: A measurement of the extent of a given cancer. Generally
clinical stage estimates how extensive a cancer is based on physical
exam and xrays, while pathological stage evaluates the
extensiveness by microscopic evaluation. In general the more
advanced the stage the worse the expected prognosis

Systemic: Throughout the body

Ureter: Tubular structure used to transmit urine from the kidney to
the bladder

Urethra: Tubular structure used to drain urine from the bladder. The
prostate surrounds the urethra at the base of the bladder

Vas Deferens: A thin tube connecting the testicle to the prostate in
order to facilitate sperm deposition into seminal fluid

Vertebra: The bones that surround and support the spinal cord and
allow for support and flexibility of the back
Information About Prostate Cancer

Prostate Cancer Prevention
Many studies have been done to evaluate the possibility of preventing
prostate cancer. A large United States study recently evaluated the
effect of Finasteride (Proscar) on the development of prostate cancer.
This study involved nearly 19,000 men and found that when this
medication taken daily for 7 years, it decreased the incidence of
prostate cancer from 24.4% to 18.4%. The medication studied
decreases the production of dihydrotestosterone (DHT), the most
potent form of testosterone. Patients on finasteride frequently
experience a shrinkage of the prostate gland, which can improve
urinary voiding symptoms, but also may cause sexual dysfunction in
a small proportion of men as well. Additionally, in this study, prostate
cancers that developed in the men taking Finasteride appeared to be slightly more aggressive than in the men taking placebo [1]. Soy is currently being evaluated in the prevention of prostate cancer. Prostate cancer prevalence is significantly lower in Asian men, particularly those who consume a high-soy diet. Soy is thought to be a naturally-occurring 5-alpha reductase inhibitor [2]. Selenium and vitamin E have both been seen to decrease the incidence of prostate cancer in studies evaluating the effect of these supplements on lung cancer [3,4]. Prospective evaluation of the effect of selenium and vitamin E on the development of prostate cancer is currently underway. Lycopene, an antioxidant found in processed red tomatoes (in addition to other sources) has also shown some anti-tumor activity and is actively being studied in the prevention and treatment of prostate cancer [5]. The correlation between testosterone levels, obesity, and prostate cancer is still being investigated. While traditional studies have shown testosterone stimulates the growth of prostate cancer, recent studies indicate low testosterone may be a risk factor for prostate cancer. Some speculate low testosterone may mask prostate cancer by keeping BPH (benign prostatic hypertrophy) to a minimum and thereby suppressing the baseline PSA [6]. Some studies even show that those cancers found in men with low testosterone levels may be more aggressive than those in men with normal testosterone [7]. There are many studies that show no link between obesity and prostate cancer, but others find that obese men who develop prostate cancer have a worse outcome [8]. This may be secondary to increased positive surgical margins (with more difficult surgery) or because of a relative decrease in circulating testosterone (heavier patients make more proteins that bind to testosterone, making it less active) [9]. Studies are ongoing evaluating the signaling cascades induced by some of the agents felt to be active in prostate cancer as well as genetic combinations that may make some individuals more prone to the development of prostate cancer [10-15]. Screening for Prostate Cancer
PSA became approved by the United States’ Food and Drug
Administration in 1986 to follow patients who had developed prostate
cancer and in 1994 to screen for prostate cancer. The rate of
mortality (or death) from prostate cancer has declined from
41,000/year in 1996 to under 32,000/year in 2000 with the use of
PSA and prostate cancer screening [16]. Cancers that are detected
with PSA screening are smaller, with less likelihood of spread to other
organs or outside the prostate than cancers detected before PSA
screening. In 1986, 2/3 newly diagnosed prostate cancers were
metastatic (40%) or extracapsular (25%) [17, 18], whereas in 2003,
only 2-4% of newly diagnoses prostate cancers were metastatic and
only 1/3 were large, locally extensive, or of high grade [19, 20]. This
effect is called downstaging. Unfortunately, however, PSA screening
has not resulted in fewer low-grade cancers. Approximately 15% of
cancers are found to be high grade cancers (Gleason’s sum 8-10)
with or without screening. This may be due to inherent genetic
potential of these tumors [21].
The current recommendations by the American Urological
Association are that men over 50 have a PSA test and digital rectal
exam annually if a patient has no family history of prostate cancer or
African-American heritage. Men who do have a family history or
prostate cancer or African American heritage should begin the same
screening regimen at age 40.
Although PSA is not perfect (15% of patients with a PSA in the
normal range were found to have prostate cancer on biopsy in one
recent study [1], advances have been made to improve the sensitivity
and specificity of PSA. By lowering the threshold of PSA to 2.5
(especially in relatively younger men), the sensitivity of PSA is
improved and fewer false negatives are seen [22]. Similarly, by using
the percentage of free PSA (that which is unbound to other proteins
in the blood), complexed PSA (that which is bound to only certain
proteins in the blood), or pro-PSA (a precursor protein to PSA) the
specificity of PSA can be improved thereby decreasing the amount of
unnecessary biopsies are performed on men who do not have
prostate cancer [23].
Although it has yet to be proven definitively that screening for
prostate cancer improves an overall mortality, it has been clearly
shown that over 50% of patients with low-grade, organ confined
prostate cancer develop metastases at 15 years if no treatment is
undertaken [24]. Additionally, it has been shown that death from
prostate cancer and the development of metastases (or spread) from
prostate cancer is considerably less when surgical treatment is
performed for prostate cancer as opposed to watching the cancer
[25].
Different laboratories use different antibodies to detect PSA levels.
Some lab antibodies are more sensitive than others, so it is
recommended to have the same lab monitor PSA values over time
[26]. Additionally there are some studies that show PSA values may
change following sexual activity so it is also recommended to abstain
from sexual activity for 24 hours prior to a PSA blood draw for the
most accurate results [27]. It was also previously thought that a
digital rectal exam could raise the serum PSA value, although most
feel this increase is probably not of statistical significance.
The recommended progression for patients with an elevated PSA is
to proceed with an ultrasound-guided prostate biopsy of the prostate
if the patient’s life expectancy exceeds ten years.

Staging Prostate Cancer and Predicting Prognosis
One of the first factors to consider after a diagnosis of prostate
cancer is establsihed is the aggressiveness of the tumor.
Aggressiveness or grade of prostate cancer is measured on a 10
point scale. This aggressiveness is determined on microscopic
evaluation of the biopsy cores and is made up of two numbers, each
representing the most common patterns of cancer seen
microscopically. This Gleason’s sum correlates well with prostate
cancer prognosis. In general, a Gleason’s sum of 2-6 is thought to
represent a low-risk cancer, a Gleason’s sum of 7 cancer represents
a cancer of intermediate risk, and a cancer graded with a Gleason’s
sum of 8-10 represents high-risk disease.
In addition to microscopic grading, it is also important to understand
the extent (or stage) of prostate cancer. Staging is generally
performed by physical exam (digital rectal exam). The stages that
can be detected on physical exam are stage T1, T2 and rarely stage T3b. A stage T1 cancer is a cancer that is not evident on digital rectal exam. A T2 cancer is a cancer that can be felt on digital exam, either on one side (T2a) or both sides (T2b of the prostate). And, although rare, a T3b cancer is one that feels as though it invades the seminal vesicles, or fluid-storing sacks on the back of the prostate. In addition to local staging within the prostate, an effort is also made to stage the extent of prostate cancer outside of the prostate as well. The most frequent areas of prostate cancer spread (or metastasis) are to the surrounding lymph nodes (which are not able to be felt from outside the body) and bony skeleton. For patients with high-grade or clinically high-stage disease, a clinician may recommend a CT (computerized tomography) or bone scan to evaluate for external spread. These are generally not considered necessary in patients with low-risk disease. In patients who undergo surgery for prostate cancer (prostatectomy) the clinical stage is replaced by a more accurate pathological stage. With careful microscopic examination, the exact extent of the cancer can be identified. PSA and percentage of biopsy cores found to harbor cancer are also important prognostic variables predicting prostate cancer outcome. In general, PSA values less than 10ng/ml indicators of lower-risk disease, PSA values between 10-20 ng/ml are indicators of intermediate-risk disease, and PSA values higher than 20 are indicators of high-risk disease. In addition, if less than a third of all biopsy tissue submitted for microscopic review harbors cancer, the cancer is predicted to be of lower risk, if between 33 and 50% of the submitted tissue harbors cancer the disease is felt to be of intermediate risk, and if greater than 50% of the tissue submitted contains cancer, the cancer is considered higher risk. Many tables and configurations have been developed that attempt to account for these four independently predictive variables and predict prognosis (tumor stage, grade, PSA and percentage of biopsy cores positive). In general, patients with low-risk features by all four measures are candidates for all treatment options (including watchful waiting in older patients, surgery, radiation including radioactive seed placement (or brachytherapy), as well as cryotherapy (or freezing). Patients considered intermediate risk are generally counseled against watchful waiting (if a 10-15 year life expectancy is predicted) or brachytherapy (which does not appear to work as well as a solitary
treatment in intermediate- and high-risk cancer). Finally, men with
high-risk disease should understand that they have significant innate
risk of cancer recurrence after treatment and that multiple types of
treatments may be necessary. Additionally, these men may want to
consider enrollment in clinical trials investigating more effective first-
line therapies for high-risk prostate cancer.
The most recent data to be added to this prognostic armamentarium
for prognostication is that of the PSA doubling time. This number can
be calculated using several PSA values over time and gives one an
idea of how rapidly the cancer volume (reflected by PSA) is doubling.
Patients with a PSA doubling time of less than 6 months are also
considered high-risk and may also wish to consider systemic therapy
or participation in experimental protocols [28].
In general, once prostate cancer has spread outside the prostate, it is
generally felt that the cost of localized treatment does not improve
survival enough to justify its risks. A recent retrospective study
questions this dogma and suggests localized treatment even in
patients with metastatic disease may prolong survival [29].

Surgery and Prostate Cancer
Surgery was the initial treatment described for prostate cancer and
continues to be the option chosen by most men with prostate cancer
[30]. Although other treatment options may have similar cure rates to
surgery, no other treatment has ever proven to be superior to surgery
for controlling prostate cancer.
The benefits of surgery include: complete pathological staging, with
no need to administer hormones (or androgen deprivation) prior to
surgery, the possibility of effective, low-risk treatments in follow-up if
prostate cancer recurs after surgery, a straight-forward follow-up for
cancer following treatment, a relatively low rate of erectile dysfunction
with treatment, and the absence of inducing additional cancers in
surrounding organs with treatment. In general, surgical treatment for
low-risk prostate cancer yields a 94% 10-year disease-free survival, a
70-85% 10-year disease-free survival for intermediate-risk prostate
cancer (Gleason’s 3+4 cancers perform more favorably than
Gleason’s 4+3 cancers) and a 10-50% 10-year disease-free survival
for high-risk prostate cancer (with stage being the most significant driver of relapse in this setting) [31]. If a cancer recurs following surgical treatment for prostate cancer, radiation can be performed with cure of the recurrent disease in approximately 45% of patients. This outcome is optimized when PSA values are below 1-2 ng/ml and are not rising rapidly, and when there no evidence of disease outside of the pelvis. Post-operative radiation appears to work better in patients with positive surgical margins, a PSA that rises slowly at atleast one year following surgery, and in patients who did not have evidence of cancer invading the seminal vesicles at the time of surgery [32]. In general, there appears to be no difference in the quality of life in patients who undergo radiation and those who do not following surgery for prostate cancer [33]. The nerve-sparing approach to prostatectomy has improved the rate of erectile dysfunction dramatically following surgery. The rate at one year of erectile dysfunction following surgery in one specialized study was only 16.5% in men with both neurovascular bundles spared and 37.2% in men with only one bundle spared at the time of surgery. Importantly, positive margin rates (suggesting that cancer may be left behind) is not more common in men undergoing the nerve sparing procedure than in those where the neurovascular bundles are removed with the prostate [34]. Additionally, the rate of total incontinence in modern series is reported to be less than 1% where the risk of stress incontinence (minor leakage with coughing or lifting) approximates 20% [35]. Patients with difficulty urinating because of a large prostate are commonly cured of this condition (BPH) as well as of their prostate cancer with surgery. Surgery can be performed laparoscopically (with small instruments) as well as through a small incision above the pubic bone. Again, this approach has never been shown to be more effective than traditional surgery although studies with relatively short follow-up show that the results may be similar [36]. With laparoscopic surgery an incision large enough to remove the prostate (2-3inches) is still required to remove the prostate after it has been dissected from the body. Laparocopic surgery may be performed with or without the assistance of an operating robot. The usual hospital stay following traditional or laparoscopic radical
prostatectomy is 1-2 nights. A catheter is left in place while the
connection between the bladder and the urethra heals for 7-14 days.
Continence slowly improves as a patient learns to rely on his external
sphincter since the internal sphincter required removal with the
surgery. Most patients are dry or have a tolerable amount of leakage
at 8-12. Most patients begin treatments with Viagra or another similar
medication around this time to encourage erections if they have not
already occurred spontaneously. Erectile function continues to
improve for 6-12 months following surgery.
The most important factor to consider when evaluating surgery as an
option for prostate cancer is the surgeon to perform the prostate
removal. Studies have clearly shown that those surgeons more
experienced with a particular operation are more likely to have
positive outcomes [37].

Radiation and Prostate Cancer
Radiation is another viable treatment option with the potential for cure
for patients with prostate cancer. Radiation can be given externally
or internally (with the surgical placement of radioactive seeds that
release radiation over time). External beam radiation is generally
given daily during the weekdays over a 6-7 week treatment course.
Since radiation can cause damage and cancerous changes to other
organs over time, the more exact the placement of the radiation
treatments, the fewer side effects a patient will experience. In
general, androgen deprivation (usually accomplished with an injection
with or without accompanying oral tablets) should be used in
conjunction with (and usually beginning a few months before)
external beam radiation. Many studies have shown an improved
survival when these two treatment modalities are used in combination
[38-43]. It is thought that androgen deprivation may help sensitize
cancer cells to the effects of radiation. Unfortunatley, androgen
deprivation can cause long-lasting problems with erections in a small
percentage of patients even after treatment is over [44], as can
radiation (generally found to be 50% with external beam radiation).
Brachytherapy (or “seed” radiation) is recommended for patients with
low-risk prostate cancer and can be used without the need for
concurrent androgen deprivation. Brachytherapy studies have shown
similar cancer control rates to external beam radiation or surgery in patients with low-risk disease [45]. Brachytherapy initially appeared to have a less damaging effect on erectile function than surgery or external-beam radiation [46]. However, long-term results suggest that all three modalities may have a similar effect on erectile function [47]. Although total incontinence is not seen following treatment with radiation, patients can suffer from urinary frequency from bladder irritation or difficulty voiding secondary to the inflammation of the prostate around the urethra with treatment. It is advised that patients with extreme difficulty emptying their bladders should not undergo treatment with brachytherapy unless they are counseled that catheterization may be required (at least temporarily) [48]. The risk of incontinence in patients requiring removal of obstructing tissue after brachytherapy may be increased over those who have not had brachytherapy [*]. The risk of the development of secondary cancers from radiation is difficult to evaluate since these cancers can appear years to decades after radiation treatment. One study estimates the risk of bladder cancer in the adult population to be 3% and states that this may reach 5% in patients who have undergone pelvic irradiation [49]. There are many long-term studies reporting the results of external beam radiation (EBXRT) for prostate cancer. One study finds the 10-year disease-free recurrence rate for patients with low-risk disease is 54% following EBXRT, while this rate is 42% for patients with intermediate-risk disease, and 40% for patients with high-risk disease. Clinical studies are ongoing to find biological markers to predict who may best respond to radiation [51, 52]. A recurrence of prostate cancer in patients who have undergone radiation is sometimes difficult to detect as PSA values can fluctuate after treatment (particularly after brachytherapy). After radiation, PSA can also take a year or longer to decrease (or nadir), and values other than zero (or undectable) may still not imply cancer. The accepted definition of radiation failure is 3 consecutive rises in PSA values separated by at least a month. Although prostate biopsies can still show false positive results within two years of treatment with radiation therapy, the recommended evaluation for a continually
increasing PSA following radiation is prostate biopsy.
Although surgery is more difficult following radiation, in patients who
fail treatment with radiation, surgery can be offered with an up to 66%
cure rate and up to a 66% continence rate at some centers[53].
Cryotherapy is another salvage treatment for patients who have failed
radiation and appears to have similar cancer control rates to surgery
– at least in the short term [54]. Androgen deprivation can also
offered in this setting although without curative intent.
Cryotherapy and Prostate Cancer
Cryotherapy has undergone significant evolution since its initial use in
the 1960’s. The use of transrectal ultrasound monitoring,
temperature-sensing thermocouples, and a urethral warming device
has significantly reduced the risk of recto-prostatic fistulae
(unintended connections between the urethra and rectum), stress
urinary incontinence, and urethral obstruction or sloughing.
Permanent erectile dysfunction rates, however, remain in the 85-96%
range [55,56].
The data remain immature regarding the long-term efficacy of
cryotherapy. Short-term data, however, suggest that cryotherapy
may have cure rates near that of surgery or radiation. Cryotherapy,
as mentioned above can also be used in cases where cancer has
recurred following radiation [57].
Cryotherapy is performed in the operating room but patients are
discharged home following the procedure. A tube is generally placed
into the bladder at the time of surgery to allow urine to pass while the
swelling of the prostate from treatment resolves. This tube is
generally in place for 10-14 days. Stress incontinence is seen in 1-
6% of patients, rectal pain is experienced by 10-30% of patients.
Cancer recurrences have been seen in 30% of patients at nine
months (when patients with all grades of cancer, PSA and Gleason
scores are considered, as well as those who are treated following
radiation failure) [56]. In general, PSA values that fall below 0.1ng/ml
following cryotherapy are more likely to predict a disease-free status.
Hormones (Androgen Deprivation), Bisphosphonates, and
Prostate Cancer
Androgen deprivation is generally used for palliative care in patients
with prostate cancer. Testosterone excels the growth of prostate
cancer and very low levels of testosterone can slow the growth and
drop a patient’s PSA. Traditionally this was accomplished by
orchiectomy (a surgical procedure whereby the testicles are
removed) however, the same effect can now be accomplished by
injections and/or oral tablets.
Injectable agents, in general, are classified as leutinizing-hormone
releasing hormone (LHRH) agonsist. These alter the signal that
causes testosterone to be produced and are available in
intramuscular injectable, subcutaneous pellet, and subcutaneous
depot form and are given at monthly, quarterly, or triannual intervals.
The main side effects of LHRH agonists include hot flashes and
erectile dysfunction. Additional complaints include fatigue, mental
status changes, decreased muscle mass and increased body fat, as
well as osteoporosis with extended usage. Despite these drawbacks,
many patients tolerate LHRH agonist therapies for many years
without difficulty.
Oral medications called anti-androgens block any testosterone that is
circulating in the bloodstream. And can be taken with injectable
LHRH agonists, at the initiation of LHRH agonist treatment, or alone.
The advantage of the combination with LHRH agonists is real, but
small and can be costly in terms of side effects and financial cost
[58]. Anti-androgens should always be used at the initiation of LHRH
injections as LHRH agonists can cause a flare in the serum
testosterone which can have significant negative effects. Some
studies have evaluated anti-androgens alone, as this regimen has no
complications of osteoporosis, no complications of mental status
changes or increased body fat composition, and a significant less
proportion of erectile dysfunction. However, this medication, when
used alone, can cause significant irreversible breast growth and
tenderness. Most doctors prescribe a short-course of pre-treatment
breast radiation before beginning anti-androgen monotherapy to
attempt to avoid this complication, which has been documented to be
helpful in this arena [59]. Although some studies show promising
results with anti-androgen monotherapy [60], most data suggest it is not as beneficial as LHRH agonist therapy [61]. A new medication was introduced in 2004 which is considered an LHRH antagonist. This is also an injectable agent and does not require the initial concominant 2-week treatment with anti-androgen medication. The side effects are similar to those of LHRH agonists. Current international prospective trials are currently evaluating androgen deprivation given on an intermittent schedule in the hopes to improve outcome and decrease side effects. Although side effects do appear to be lessened with intermittent androgen deprivation, no studies have shown an improved outcome from a cancer standpoint [62]. A form of androgen deprivation (usually LHRH agonist treatment alone) should always be used with external beam radiation. Several studies have shown this to improve outcomes significantly [63,64,65,66]. On the other hand, androgen deprivation prior to surgery does not appear to improve the ultimate outcome and is generally not recommended [67,68]. Most agree that androgen deprivation is also not required with brachytherapy or seed placement for low-grade disease of the prostate. Data is still being evaluated for the benefit of androgen deprivation and cryotherapy. There has been no proven survival advantage for beginning androgen deprivation earlier rather than later if a patient’s PSA begins to rise following definitive treatment for prostate cancer [69]. However, studies do show that for those men diagnosed with prostate cancer in the lymph nodes at the time of surgery, immediate and continuous androgen deprivation improves survival. Additionally it has been shown that earlier androgen deprivation may improve urinary symptoms and decrease rare complications of prostate cancer such as kidney failure from blocked ureters or spinal cord compression from vertebral fractures [70]. Bisphosphonates are inhibitors of the cells which break down bones and are frequently used to treat osteoporosis. A potent new intravenous bisphosponate has been studied in men with metastatic prostate cancer to the bones and these studies show that clearly, intravenous bisphosphonates (zoledronic acid or zometa) given
regularly can decrease the risk of bony fractures from these
metastases [71,72]. Bisphosphonates should be considered in men
with evidence of osteoporosis or metastatic disease. The diagnosis
of osteoporosis should be investigated in men maintained on
androgen deprivation for over 2-3 years.
Androgen Independent Prostate Cancer and Clinical Trials
Once a patient has been on androgen deprivation treatment for an
extended period of time, prostate cancer tends to progress in spite of
androgen deprivation. In this scenario, blood levels of testosterone
are verified to be low and anti-androgen tablets are added if they
have not been used in the past. If a patient has been taking anti-
androgen tablets, these are discontinued, as rarely anti-androgen
tablets can serve to increase the activity of an androgen receptor.
Once these conservative measures have been tried, a patient is
considered to have “androgen independent or insensitive prostate
cancer.” This condition is also referred to as hormone refractory
prostate cancer. Certain chemotherapeutic combinations have been
shown to improve survival in androgen independent prostate cancer,
such as docetaxol and estramustine [73]. Mitoxantrone and
prednisone has also been used in this setting and has been shown to
improve the quality of life in patients with this condition. A large
multinational trial is evaluating this combination given prior to the
development of androgen independent disease in patients with high
risk features in the hope to improve overall survival from prostate
cancer.
Estrogen can also be tried in patients with prostate cancer which is
progressing despite the use of traditional androgen deprivation, or
can even be used prior to the development of androgen
independence, but should be used carefully due to the increased risk
of blood clots if given alone and/or in high doses [74]. Since none of
these options provide a dramatic improvement in outcome and since
many are difficult treatments to tolerate, many clinical trials continue
to investigate the best treatment option for patients with this
condition. Since no clinical trial includes any therapy that is thought
to be worse than the standard of care, clinical trial participation is
encouraged to provide for possible improved outcomes in patients
with a given condition as well as future patients who may develop the
condition.
References:
1. Thompson IM, Phyllis JG, Tangen CM et al: The influence of finasteride on
the development of prostate cancer. N Engl J Med 349(3): 213-22. 2. Moyad MA. Soy, disease prevention, and prostate cancer. Semin Urol 3. Duffield-Lillico AJ, Dalkin BL, Reid ME et al.: Selenium supplementation, baseline plasma selenium status and incidence of prostate cancer: an analysis of the complete treatment. period of the Nutritional Prevention of cancer Trial. BJU Int 2003; 91(7)608-12. 4. Heinonen OP, Albanes D, Virtamo J, et al. Prostate cancer and supplementation with alpha-tocopherol and beta-carotene: incidence and mortality in a controlled trial. J NCI 1998; 90(6):440-6. 5. Barqawi A, Thompson IM and Crawford ED. Prostate cancer chemoprevention: an overview of United States trials. J Urol 2004;171(2 Pt 2):S5-8. 6. Giovannucci E, Rimm EB, Liu Y et al: Body mass index and risk of prostate cancer in U.S. health professionals. J Natl Cancer Inst 2003; 95(16):1240-4. 7. Schatzl G, Madersbacher S, Thurridl T, et al. High-grade prostate cancer is associated with low serum testosterone levels. Prostate 2001; 47(1):52 8. Freedlan SJ, Aronson WJ, Kane CJ, et al. Impact of obsesity on biochemical control after radical prostatectomy for clinically localized prostate cancer: a report by the Shared Equal Access Regional Cancer Hospital database study group. JCO 2004; 22(3):446-53. 9. Le Marchand L, Kolonel LN, Wilkens LR, et al. Animal fat consumption and prostate cancer: a prospective study in Hawaii. Epidemiology 1994; 5:276. 10. Shuch B, Mikhail M, Satagopan J, et al. Racial disparity of epidermal growth factor receptor expression in prostate cancer. JCO 2004; 22(23):4725-4729. 11. Van Gils CH, Bostick RM, Stern MC et al: Efferences in base excision repair capacity may modulate the effect of dietary antioxidant intake on prostate cancer risk: an example of polymorphisms in the XRCC1 gene. Cancer Epidemiol Biomarkers Prev 2002 11(11):1279-84. 12. Gronberg H, Isaacs SD, Smith JR et al. Characteristics of prostate cancer in families potentially liked to the hereditary prostate cancer 1 (HPC1) locus. JAMA 1997; 278:1251. 13. Casey G, Neville PJ, Plummer Y, et al: RNASEL Arg462Gln variant is implicated in up to 13% of prostate cancer cases. Nat Genet 2002; 32:581-3 14. Li LC, Carroll P, and Dahiya R. Epigenetic changes in prostate cancer: implication for diagnosis and treatment. JNCI 2005; 97(2):103-115. 15. Fordyce CA, Heaphy CM, Joste NE, et al. Association between cancer-free survival and telomere DNA content in prostate tumors. J Urol 2005; 173(2):610-4. 16. American Cancer Society. Mortality Statistics 1995 – 2000. 17. McLaughlin AP, Saltzstein SL, McCullough DL, et al. Prostatic carcinoma: incidence and location of unsuspected lymphatic metastases. Journal of Urology 1976; 115(1):89-94. 18. Trends in patterns of care for prostate cancer, 1974-1983: Results of surveys by the American College of Surgeons. J Urol 1986; 136:416-421. 19. Ries L. Bathesda Md: NCI, 2002. 20. Catalona W.J., Smith D.S. and Ratliff T.L. et al. Detection of organ-confined prostate cancer is increased through prostate-specific antigen-based screening. JAMA 1993, 270:948-954. 21. Stamey T, Donaldson N, Yemoto AN, et al. Histological and clinical findings in the United States treated with RRP; histo significance of annual changes. J Urol 1998;160(6-II):2412-2417. 22. Catalona W, Richie J, Ahmann F, et al. Comparison of digital rectal examination and serum prostate specific antigen in the early detection of prostate cancer: results of a multicenter trial of 6,630 men. J Urol. 1994;151:1283-1290. 23. Catalona WJ et al. Serum Pro-PSA preferentially detects aggressive CaP in men with PSA of 2-4. J Urol 2004; 171(6):2239. 24. Johansson JE, Andren O, Andersson SO et al. Natural history of early, localized prostate cancer. JAMA 2004; 291(22):2713-9. 25. Holmberg L, Bill-Axelson A, Helgesen F et al. A randomized trial comparing radical prostatectomy with watchful waiting in early prostate cancer. N Engl J Med 2002; 347(11):781-9. 26. Blasea, AB et al Five PSA Methods Compared by Assay Samples w/ Defined 27. M Tchetgen. Ejaculation increases the serum PSA concentration. Urol 28. Zelefsky MJ, Ben-Porat L, Scher HI, et al. Outcome predictors for the increasing PSA state after definitive external-beam radiotherapy for prostate cancer. JCO 2005; 23(4): 826-31. 29. Thompson IM, Tangen C, Basler J, et al: Impact of previous local treatment for prostate cacner on subsequent metastatic disease. J Urol 2002; 168(3): 1008-12. 30. Pollack A, Grignon DJ, Heydon KH et al. Prostate cancer DNA ploidy and response to salvage hormone therapy after radiotherapy with or without short-term total androgen blockade: an analysis of RTOG 86-10. J Clin Oncol 2003; 21(7):1238-48. 31. Han M, Partin AW, and Zahurak M. Biochemical (prostate specific antigen) recurrence probability following radical prostatectomy for clinically localized prostate cancer. J Urol 2003; 169(2):517-23. 32. Petrovich Z, Lieskovdky B, Langholz G, et al: Postoperative radiotherapy in 423 patients with pT3N0 prostate cancer. Int J Radiat Oncol Biol Phys 2002; 52:600-9. 33. Anscher MS, Clough R, Dodge R: Radiotherapy for a rising prostate-specific antigen after radical prostatectomy: The first 10 years. Int J Radiat Oncol Biol Phys 2000; 48:369-75. 34. Hernandez DJ, Epstein JI, Trock BJ, et al. Radical retropubic prostatectomy. How often do experienced surgeons have positive surgical margins when ther is extraprostateic extension in the region of the neurovascular bundle? J Urol 2005; 173(20): 446-9. 35. Lepor H and Kaci L. The impact of open radical retropubic prostatectomy on continence and lower urinary tract symptoms: a prospective assessment using validated self-administered outcome instruments. J Urol 2004; 171(3):1216-9. 36. Touijer AK and Guillonneau B: Laproscopic radical prostatectomy. Urol 37. Begg CB, Riedel ER, Bach PB et al. Variations in morbidity after radical prostatectomy. NEJM 2002; 346(15):1138-44. 38. Roach M III, DeSilvo M, Lawton C, et al: Phase II trial comparing whole-pelvic versus prostate-only radiotherapy and neoadjuvant verses adjuvant combined androgen supression: Radiation Therapy Oncology Group 9413. J Clin Oncol 2003; 21(10): 1904-11. 39. Lawton CA, Winter, Grignon D, et al: androgen suppression plus radiation versus radiation alone for patients with D1/pathologic node-positive adenocarcinoma of the prostate: updated results based on national prospective randomized trial Radiation Therapy Oncology Group 85-31. 40. Shipley WU, Lu JD, Pilepich MV et al: Effect of a short course of neoadjuvant hormonal therapy on the response to subsequent androgen suppression in prostate cancer patients with relapse after radiotherapy: a secondary analysis of the randomized protocol RTOG 86-10. Int J Radiat Oncol Biol Phys 2002; 54(5):1302-10. 41. Bolla et al: Results of a randomized trial of external beam therapy plus immediate androgen suppression verses external beam therapy alone. Lancet 2002; 360:103-6. 42. D’Amico AV, Manola J< Loffredo M, et al. 6-month androgen suppression plus radiation therapy vs radiation therapy alone for patients with clinically localized prostate cancer: a randomized controlled trial. JAMA 2004; 292(7):821-7. 43. Cooperberg MR, Grossfeld GD, Lubeck DP, et al: National practice patterns and time trends in androgen ablation for localized prostate cancer. Journal of the National Cancer Institute 2003; 95(13):981-9. 44. Rashid MH and Chaudhary UB. Intermittent androgen deprivation therapy for prostate cancer. Oncol 2004; 9(3):295-301. 45. Quaranta BP, Marks LB, Anscher MS. Comparing radical prostatectomy and brachytherapy for localized prostate cancer. Onc (Hunntingt). 2004; 18(13):1582-5. 46. Stock RG, Kao J, and Stone NN. Penile erectile function after permanent radioactive seed implantation for treatment of prostate cancer. J Urol 2001;165(2):436-9. 47. Raina R, Agarwal A, Goyal KK et al. Long-term potency after iodine-125 radiotherapy for prostate cancer and role of sildenafil citrate. Urol 2003; 62(6):1103-8. 48. Williams SG. Millar JL. Duchesne GM. Factors predicting for urinary morbidity following 125 iodine transperineal prostate brachytherapy. Rad & Onc 2004; 73(1):33-8. 49. Arai T, Nakano T, Fukuhisa K et al. Second cancer after radiation therapy for cancer of the uterine cervix. Cancer 1991; 67(2):398-405, 1991. 50. Powell CR, Huisman TK, Riffenburgh RH et al. Outcome for surgically staged localized prostate cancer treated with external beam radiation therapy. J Urol 1997 157(5):1754-9. 51. Pollack A, DeSilvio M, Khor LY, et al. Ki-67 staining is a strong predictor of distant metastasis and mortality for men with prostate cancer treated with radiotherapy plus androgen deprivation: Radiation Therapy Oncology Group Trial 92-02. 52. Shariat SF, Anwuri VA, Lam DJ, et al. Association of preoperative plasma levels of vascular endothelial growth factor and soluble vascular cell adhesion molecule-1 with lymph node status and biochemical progression after radical prostatectomy. 53. Stephenson AJ, Scardino PT, Bianco FJ JR, et al. Salvage therapy for locally recurrent prostate cancer after external beam radiotherapy. Curr Treatment Op in Onc 2004; 5(5):357-65. 54. Touma NJ, Izawa IL, Chin JL, et al. Current status of local salvage therapies following radiation failure for prostate cancer. J Urol 2005; 173(20: 373-9. 55. Saliken JC. Donnelly BJ. Brasher P. Ali-Ridha N. Ernst S. Robinson J. Outcome and safety of transrectal US-guided percutaneous cryotherapy for localized prostate cancer. Journal of Vascular & Interventional Radiology 1999; 10(2 Pt 1):199-208. 56. De La Taille A, Benson MC, Bagiella E, et al. Cryoablation for clinically localized prostate cancer using an argon-based system: complication rates and biochemical recurrence. BJU International 2000; 85(3):281-6. 57. Touma NJ, Izawa JI, and Chin JL. Current status of local salvage therapies following radiation failure for prostate cancer. J Urol 2005; 173(2):373-9. 58. Samson DJ, Seidenfeld J, Schmitt B et al. Systematic review and meta- analysis of monotherapy compared with combined androgen blockade for patients with advanced prostate carcinoma. Cancer 2002; 95(2):361-76. 59. Widmark A, Fossa SD, Lundmo P, et al: Does prophylactic breast irradiation prevent antiandrogen-induced gynecomastia? Evalution of 253 patients in the randomized Scandinavian trial SPCG-7/SFUO-3. Urology 2003; 61(1):145-51. 60. See WA, McLeod DG, Wirth MP et al: Bicalutamide as immediate therapy either alone or as adjuvant to standard care of patients with localized or locally advanced prostate cancer: first analysis of the early prostate cancer program. Journal of Urology 2002; 168:429-35. 61. Boccardo F, Barichello M, Battaglia M et al: Bicalutamide monotherapy versus flutamide plus goserelin in prostate cancer: updated results of a multicentric trial. Eur Urol 2002; 42(5):481-90. 62. Olsson CA, Dennis JJ, Miller GL et al: 2003 Annual Meeting Convention Highlights. Medical Association Communications 2003; page 15. 63. Lawton CA, Winter, Grignon D, et al: androgen suppression plus radiation versus radiation alone for patients with D1/pathologic node-positive adenocarcinoma of the prostate: updated results based on national prospective randomized trial Radiation Therapy Oncology Group 85-31. 64. Shipley WU, Lu JD, Pilepich MV et al: Effect of a short course of neoadjuvant hormonal therapy on the response to subsequent androgen suppression in prostate cancer patients with relapse after radiotherapy: a secondary analysis of the randomized protocol RTOG 86-10. Int J Radiat Oncol Biol Phys 2002; 54(5):1302-10. 65. Bolla et al: Results of a randomized trial of external beam therapy plus immediate androgen suppression verses external beam therapy alone. Lancet 2002; 360:103-6. 66. D’Amico AV, Manola J< Loffredo M, et al. 6-month androgen suppression plus radiation therapy vs radiation therapy alone for patients with clinically localized prostate cancer: a randomized controlled trial. JAMA 2004; 292(7):821-7. 67. Yoshimura K, Sumiyoshi Y, Hashimura T, et al: Neoadjuvant flutamide monotherapy for locally confined prostate cancer. Int J Urol 2003; 10(4) 190-5. 68. Aus G, Abrahamsson PA, Ahlgren G, et al: Three-month neoadjuvant hormonal therapy before radical prostatectomy: a 7-year follow-up of a randomized controlled trial. BJU Int 2002; 90(6):651-6. 69. Studer UE, Hauri D, Hanselmann S, et al. Immediate versus deferred hormonal treatment for patients with prostate cancer who are not suitable for curative local treatment: results of the randomized trial SAKK 08/88. JCO 2004; 22(20):4109-18. 70. The Medical Research Council Prostate Cancer Working Party Investigators Group. Immediate versus deferred treatment for advanced prostate cancer: initial results of the Medical Research Council Trial. Br J Urol 1997; 79:235-46. 71. Smith MR, Estham J, Gleason DM, et al: Randomized controlled trial of zolendronic acid to prevent bone loss in men receiving androgen deprivation therapy for nonmetastatic prostate cancer. J Urol 2003; 169(6):2008-12. 72. Saad F, Gleason DM, Murray R, et al: A randomized, placebo-controlled trial of zoledronic acid in patients with hormone-refractory metastatic prostate carcinoma. J Natl Cancer Inst 2002; 94(19):1458-68. 73. Petrylak DP, Tangen CM, Hussain MH, et al. Docetaxel and estramustine compared with mitoxantrone and prednisone for advanced refractory prostate cancer. NEJM 2004; 351(15):1513-20. 74. Scherr DS. Pitts WR Jr. The nonsteroidal effects of diethylstilbestrol: the rationale for androgen deprivation therapy without estrogen deprivation in the treatment of prostate cancer. Journal of Urology 2003; 170(5):1703-8.

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