- •Table of Contents
- •Copyright
- •Contributors
- •How to Use this Study Guide
- •Questions
- •Answers
- •Questions
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- •Questions
- •Answers
- •4: Outcomes Research
- •Questions
- •Answers
- •5: Core Principles of Perioperative Care
- •Questions
- •Answers
- •Questions
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- •7: Principles of Urologic Endoscopy
- •Questions
- •Answers
- •8: Percutaneous Approaches to the Upper Urinary Tract Collecting System
- •Questions
- •Answers
- •Questions
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- •Questions
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- •12: Infections of the Urinary Tract
- •Questions
- •Answers
- •Questions
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- •15: Sexually Transmitted Diseases
- •Questions
- •Answers
- •Questions
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- •20: Principles of Tissue Engineering
- •Questions
- •Answers
- •Questions
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- •22: Male Reproductive Physiology
- •Questions
- •Answers
- •Questions
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- •24: Male Infertility
- •Questions
- •Answers
- •Questions
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- •Questions
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- •Questions
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- •28: Priapism
- •Questions
- •Answers
- •Questions
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- •30: Surgery for Erectile Dysfunction
- •Questions
- •Answers
- •Questions
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- •Questions
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- •Questions
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- •34: Neoplasms of the Testis
- •Questions
- •Answers
- •35: Surgery of Testicular Tumors
- •Questions
- •Answers
- •36: Laparoscopic and Robotic-Assisted Retroperitoneal Lymphadenectomy for Testicular Tumors
- •Questions
- •Answers
- •37: Tumors of the Penis
- •Questions
- •Answers
- •38: Tumors of the Urethra
- •Questions
- •Answers
- •39: Inguinal Node Dissection
- •Questions
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- •40: Surgery of the Penis and Urethra
- •Questions
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- •Questions
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- •47: Renal Transplantation
- •Questions
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- •Questions
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- •Questions
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- •50: Upper Urinary Tract Trauma
- •Questions
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- •53: Strategies for Nonmedical Management of Upper Urinary Tract Calculi
- •Questions
- •Answers
- •54: Surgical Management for Upper Urinary Tract Calculi
- •Questions
- •Answers
- •55: Lower Urinary Tract Calculi
- •Questions
- •Answers
- •56: Benign Renal Tumors
- •Questions
- •Answers
- •57: Malignant Renal Tumors
- •Questions
- •Answers
- •Questions
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- •59: Retroperitoneal Tumors
- •Questions
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- •60: Open Surgery of the Kidney
- •Questions
- •Answers
- •Questions
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- •62: Nonsurgical Focal Therapy for Renal Tumors
- •Questions
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- •66: Surgery of the Adrenal Glands
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- •71: Evaluation and Management of Women with Urinary Incontinence and Pelvic Prolapse
- •Questions
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- •72: Evaluation and Management of Men with Urinary Incontinence
- •Questions
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- •Questions
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- •Questions
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- •76: Overactive Bladder
- •Questions
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- •77: Underactive Detrusor
- •Questions
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- •78: Nocturia
- •Questions
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- •82: Retropubic Suspension Surgery for Incontinence in Women
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- •83: Vaginal and Abdominal Reconstructive Surgery for Pelvic Organ Prolapse
- •Questions
- •Answers
- •Questions
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- •85: Complications Related to the Use of Mesh and Their Repair
- •Questions
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- •86: Injection Therapy for Urinary Incontinence
- •Questions
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- •87: Additional Therapies for Storage and Emptying Failure
- •Questions
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- •88: Aging and Geriatric Urology
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- •89: Urinary Tract Fistulae
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- •92: Tumors of the Bladder
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- •95: Transurethral and Open Surgery for Bladder Cancer
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- •99: Orthotopic Urinary Diversion
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- •108: Prostate Cancer Tumor Markers
- •Questions
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- •110: Pathology of Prostatic Neoplasia
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- •114: Open Radical Prostatectomy
- •Questions
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- •116: Radiation Therapy for Prostate Cancer
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- •117: Focal Therapy for Prostate Cancer
- •Questions
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- •119: Management of Biomedical Recurrence Following Definitive Therapy for Prostate Cancer
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- •120: Hormone Therapy for Prostate Cancer
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- •124: Perinatal Urology
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- •126: Pediatric Urogenital Imaging
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- •133: Surgery of the Ureter in Children
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- •137: Vesicoureteral Reflux
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- •138: Bladder Anomalies in Children
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- •139: Exstrophy-Epispadias Complex
- •Questions
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- •140: Prune-Belly Syndrome
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- •144: Management of Defecation Disorders
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- •147: Hypospadias
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- •Questions
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- •152: Adolescent and Transitional Urology
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- •154: Pediatric Genitourinary Trauma
- •Answers
- •Questions
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- •Questions
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120
Hormone Therapy for Prostate Cancer
Joel B. Nelson
Questions
1.The effectiveness of estrogen as a hormone therapy for prostate cancer is primarily based on:
a.direct cytotoxic effects of estrogen on prostate cancer cells.
b.competitive binding of estrogen to the androgen receptor.
c.inhibition of the conversion of cholesterol to pregnenolone.
d.desensitizing luteinizing hormone–releasing hormone (LHRH) receptors in the anterior pituitary.
e.negative feedback on luteinizing hormone (LH) secretion by the pituitary.
2.The expected response of a man to the administration of the nonsteroidal antiandrogens is:
a.LH increases, testosterone decreases, estrogen decreases.
b.LH increases, testosterone increases, estrogen decreases.
c.LH increases, testosterone increases, estrogen increases.
d.LH decreases, testosterone decreases, estrogen increases.
e.LH decreases, testosterone increases, estrogen increases.
3.All of the following therapeutic approaches for androgen axis blockade are in current clinical use, EXCEPT:
a.inhibition of androgen synthesis.
b.blocking androgen action by binding to the androgen receptor in a competitive fashion.
c.ablating the source of androgens.
d.direct inhibition of androgen receptor–mediated pathways.
e.inhibition of LHRH and LH release.
4.Nonsteroidal antiandrogens:
a.do not act as agonists for prostate cancer cells when used in combination with LHRH agonists.
b.allow long-term maintenance of erectile function and sexual activity at rates similar to men undergoing surgical castration.
c.commonly induce gastrointestinal toxicity, manifest as constipation leading, on occasion, to fecal impaction.
d.have pancreatic toxicity, ranging from reversible mild to fulminant, life-threatening suppurative pancreatitis; requires periodic monitoring of serum amylase and lipase.
e.cause fluid retention and thromboembolism in the majority of patients.
5.Which of the following nonsteroidal antiandrogens is associated with interstitial pneumonitis and a delayed adaptation to darkness after exposure to bright illumination?
a.Bicalutamide
b.Flutamide
c.Hydroxyflutamide
d.Nilutamide
e.Cyproterone acetate
6.Which of the following statements is TRUE concerning LHRH agonists?
a.Based on a review of 24 trials, involving more than 6600 patients, survival after therapy with an LHRH agonist was significantly better than after surgical castration.
b.Although depot preparations and osmotic pump devices allow dosing to extend from 28 days to 1 year, the most effective dosing regiment is daily.
c.Current LHRH agonists are based on analogues of the native LHRH decapeptide by amino acid substitutions, particularly position 6 of the peptide.
d.Widespread use of orally effective LHRH agonists has been limited by severe allergic reactions in some patients, even after previously uneventful treatment.
e.The use of LHRH agonists is limited to combined androgen blockade.
7.Each of the following has been associated with a favorable initial response to androgen deprivation therapy, EXCEPT:
a.the magnitude of the PSA decline.
b.the rapidity of the PSA decline.
c.the PSA doubling time before initiating androgen deprivation therapy (ADT).
d.the Gleason score of the primary tumor.
e.the maintenance of a detectable PSA.
8.Which of the following statements about the complications of ADT is TRUE?
a.Most men undergoing ADT have normal bone mineral density before initiating therapy, and it usually takes at least a decade of treatment before the average man will develop osteopenia.
b.Hot flashes occur in about one quarter of men on ADT but should always be treated because of the associated rare but life-threatening cardiovascular side effects.
c.Erectile dysfunction after surgical castration or use of an LHRH is common but not inevitable: Although 1 in 5 men maintain some sexual activity, only 1 in 20 maintain high levels of sexual interest (libido).
d.Because most men on ADT maintain lean muscle mass, the increase in weight is due to increases in adipose tissue.
e.Gynecomastia and mastodynia are common with estrogenic compounds and antiandrogens but are effectively treated by external beam radiation after they occur.
9.Which of the following statements about the combination of 3 months of neoadjuvant ADT before radical prostatectomy is TRUE?
a.Positive surgical margin rates are significantly reduced with ADTtreated patients.
b.There is a significant reduction in biochemical (PSA) progression with ADT-treated patients.
c.The benefit of neoadjuvant ADT appears to be in men with locally advanced disease and/or those with high-grade disease.
d.Antiandrogen monotherapy has not shown a significant reduction of biochemical failure, but LHRH agonists have demonstrated this reduction.
e.Although the results of prospective randomized studies of this combination are mixed, the overall body of evidence supports the use of ADT in this setting.
.Combined androgen blockade:
a. is designed to address the low levels of testicular androgens remaining after the use of LHRH agonists or antagonists.
b.typically uses an antiandrogens at the time of PSA rise after treatment with an LHRH agonist.
c.has not shown a survival advantage compared with an LHRH agonist alone.
d.significantly benefits men with minimally metastatic disease when used in combination with surgical castration.
e.using cyproterone acetate has a slightly worse outcome.
.Compared with deferred ADT, early ADT instituted before the development of objective metastatic disease:
a.provides an overall survival advantage in all clinical disease states.
b.has an equivalent quality of life.
c.does not increase overall death rates.
d.does not prevent the emergence of castration-resistant prostate cancer.
e.should be offered to men with PSA recurrence after radical prostatectomy because of the rapid disease progression in this clinical setting.
.In men with lymph-node metastatic prostate cancer discovered at the time of radical prostatectomy:
a.significant overall survival benefits of immediate ADT are limited to those with extrapelvic positive nodes.
b.a significant overall survival benefit of immediate ADT has been demonstrated in men who have also undergone subsequent radical prostatectomy.
c.a significant overall survival benefit of immediate ADT has been demonstrated in men who have not undergone subsequent radical prostatectomy.
d.b and c are correct
e.a, b, and c are correct
.From a strictly financial point of view, which of the following forms of ADT is the least expensive?
a.Scrotal orchiectomy
b.LHRH agonist
c.Diethylstilbestrol (DES)
d.Antiandrogen monotherapy
e.LHRH antagonist
.In a trial studying continuous ADT to intermittent ADT for men with rising PSA after radiation therapy: