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Prostate cancer is the most commonly diagnosed noncutaneous cancer in men in the United States. Treatment of men with prostate cancer commonly involves surgical, radiation, or hormone therapy. Most men with prostate cancer live for many years after diagnosis and may never suffer morbidity or mortality attributable to prostate cancer. The short-term and long-term adverse consequences of therapy are, therefore, of great importance. Adverse effects of radical prostatectomy include immediate postoperative complications and long-term urinary and sexual complications. External beam or interstitial radiation therapy in men with localized prostate cancer may lead to urinary, gastrointestinal, and sexual complications. Improvements in surgical and radiation techniques have reduced the incidence of many of these complications. Hormone treatment typically consists of androgen deprivation therapy, and consequences of such therapy may include vasomotor flushing, anemia, and bone density loss. Numerous clinical trials have studied the role of bone antiresorptive therapy for prevention of bone density loss and fractures. Other long-term consequences of androgen deprivation therapy may include adverse body composition changes and increased risk of insulin resistance, diabetes, and cardiovascular disease. Ongoing and planned clinical trials will continue to address strategies to prevent treatment-related side effects and improve quality of life for men with prostate cancer.
Prostate cancer is diagnosed in over 186,000 men in the United States and accounts for more than 28,000 deaths annually.1 Numerous modalities are involved in treating men with this condition, and a multidisciplinary approach to treatment is often beneficial. For localized prostate cancer, the most common treatments are radical prostatectomy (RP) or whole prostate radiation therapy. In more advanced disease, medical therapy is often used, and the mainstay of treatment is androgen deprivation therapy (ADT). The widespread use of each of these approaches has increased the relevance and importance of characterizing and treating the potential complications of treatment. This article will focus on management of complications from surgery, radiation, or medical therapy of prostate cancer.
RP is a standard definitive therapy for localized prostate cancer. Surgical techniques have continued to improve, and technology and surgical training have expanded the urologist's armamentarium in this arena. Options currently include open retropubic, laparoscopic (with or without robotic assistance), or perineal approaches. These procedures, in experienced hands, appear to yield equivalent oncologic outcomes.2–9 The ultimate decision as to which surgical approach should be used depends on several factors, including surgeon skill and comfort level with a particular approach; the patient's body habitus; comorbidities; previous surgical history; and, perhaps most importantly, the preoperative Gleason score and preoperative staging.
In the last 25 years, there have been considerable advances in operative and postoperative care, as well as significant modifications in the surgical technique itself. A better understanding of pelvic anatomy, including the vasculature and innervation surrounding the prostate, has led to a significant decrease in the mortality and relative morbidity for patients undergoing RP.10,11 Furthermore, improved surgical training and the establishment of centers specializing in minimally invasive surgery have increased the popularity of laparoscopic (or robotic-assisted laparoscopic) radical prostatectomy (LRP) for the treatment of localized prostate cancer. Minimally invasive techniques such as LRP have also led to a decreased length of stay, shorter convalescence, and improved cosmesis.
Regardless of the surgical approach used, there are complications inherent to the procedure itself. Complications inherent to LRP and laparoscopy itself are beyond the scope of this review and have been covered in detail elsewhere.12 Overall, complications can be divided into those that occur during and immediately after surgery (perioperative) and those that occur late after surgery (postoperative).
Patient positioning during RP requires meticulous attention to detail in order to prevent serious injury. Potential complications solely related to prolonged extrinsic compression on tissues are not uncommon.13 During patient positioning, care should be taken to pad all pressure points, including the sites of the ulnar and common peroneal nerves. Care should be taken not to hyperextend the shoulders or hips, as this may cause brachial plexus or lumbar plexus injuries.14,15 The eyes should also be protected by the anesthesia team since corneal abrasions and conjunctivitis from corneal irritation by saliva have been reported in some series.14
The most frequent cause of neurological injuries during RP, occurring in 0.5% to 1.4% of cases,12 is direct damage to nerves or traction injuries from inadequate patient positioning (see previous section). Injury to the obturator nerve is a known complication during pelvic lymphadenectomy in both RP and LRP and may result in failure of leg adduction. Care must be taken to identify visually the obturator nerve before ligation and cutting of the inferior aspect of the node bundle. If the nerve is ligated but not cut, removal of the clip is all that is necessary, although most of these patients will be symptomatic from the crush injury. Transection of the obturator nerve during RP can be repaired by reapproximating the nerve sheath with sutures.16
Small and large bowel injuries (excluding rectal injuries) are rare during radical retropubic prostatectomy (RRP) and radical perineal prostatectomy (RPP) since these are “extraperitoneal” procedures. Bowel injuries leading to perforation during LRP, however, are more common (0.5% to 1.5%) and can occur during trocar placement, during instrument exchange, or during tissue dissection; bowel injury can also result from thermal injury due to electrocautery devices. In LRP, the lateral large bowel (sigmoid and cecum) is vulnerable to injury during placement of the lateral ports and when instruments are being changed. Thermal tissue damage from a harmonic scalpel or electrocautery device, as well as arcing of the monopolar current to adjacent organs, is a common etiology of bowel injury and accounts for more than half of all laparoscopic bowel injuries.17 The most important aspect regarding bowel injuries is that they need to be identified intraoperatively. Failure to recognize these injuries when they occur can have significant morbidity and mortality. In fact, in a large study of laparoscopic entry access injuries, Chandler et al showed that delayed recognition and diagnosis of these injuries, along with age greater than 59 years, were significant predictors of fatal outcomes.18 They also noted that unrecognized bowel injuries were significantly more likely to cause death than injuries to major retroperitoneal vessels. If bowel injury is suspected in a postoperative patient, abdominal pelvic computed tomography (CT) with oral contrast is a reliable method for diagnosis.19 Alternatively, a diagnostic laparoscopy can be performed with high diagnostic accuracy in 92% to 97% of cases.20,21
Injury to the rectum is a specific type of bowel injury that should be considered separately. Rectal injury during RP has been reported in 0.3% to 3.8% of cases.10,22 During RRP and RPP, most rectal injuries occur while transecting the rectourethralis muscle.23,24 In a series of 1,000 LRP, Guillonneau et al reported 13 rectal injuries, 10 of which occurred during dissection of the posterior surface of the prostate at the apex.23 These types of injuries can also occur from thermal or electrical injury to the rectum at any point during an LRP. The main point, as in other bowel injuries, is that these need to be recognized at the time they occur in the operating room in order to minimize morbidity. Once these injuries are diagnosed, the edges of the defect should be clearly identified and closed in 2 layers.25,26 Although there is no clear evidence for this, a diverting colostomy should be considered in cases of gross fecal spillage, previous radiation, a urethrovesical anastomosis under tension, or in a patient who is chronically treated with steroids.27,28 The consequences of a missed rectal injury or of inappropriate repair can have significant morbidity and are covered elsewhere.25,29
Some degree of bleeding can be expected for any surgical procedure, and at which point operative bleeding becomes a “complication” is subject to debate. Obviously, an unplanned or unrecognized injury to a blood vessel or an injury that requires any additional intervention beyond that planned during a procedure constitutes a complication. During LRP, inadvertent injury to vessels usually occurs during trocar placement, during pelvic lymphadenectomy, or during instrument exchange. Although these types of injuries are rare in contemporary series, ranging from 0% to 1%,30–33 recognition of vessel injury during surgery is very important. A theoretical advantage of minimally invasive surgery is decreased bleeding. A reliable description of bleeding as a complication may be blood transfusion rates. Both estimated blood loss (EBL) and transfusion rates vary widely in reported LRP series, with EBL ranging from 150 mL to 1100 mL and transfusion rates ranging from 0% to 31%.31,34–40 Despite these differences, the average EBL and average transfusion rates for LRP seem to be less than those of RRP.41 Furthermore, the EBL seems to decrease with the surgeon's experience.31
The 2 major sites of bleeding during RP are from the dorsal venous plexus and from the prostatic pedicles. Adequate ligation of the former and meticulous hemostasis during the pedicle dissection will obviate most serious hemorrhage. Unrecognized venous bleeding during LRP may lead to pelvic hematoma formation. Larger hematomas may lead to recurrent fevers, infection, voiding symptoms, urinary retention, pelvic pain, anastomotic disruption, and bladder neck contracture.42,43 In these instances, it may be appropriate to drain these hematomas either through a percutaneous approach or through a small infraumbilical incision. Although not technically a bleeding complication, lymphocele is a recognized complication of lymphadenectomy as part of RP and has been noted to occur in 0.1% to 1% of patients.44 If these lead to infection with symptoms such as pain or fever, percutaneous drainage is also a good treatment modality.
Ureteral complications have been reported in 0% to 1% of patients undergoing LRP22,45 and are even less common during RRP and RPP. The ureter may be injured by thermal or electrical injury14 or by suture placement near or through the ureteral orifice at the time of urethrovesical anastomosis.
Ideally, ureteral injuries should be recognized at the time they occur. In these cases, the ureter can be repaired primarily over a ureteral stent, or a ureteroneocystostomy can be performed. Both of these techniques have been performed laparoscopically.46,47 Unrecognized ureteral orifice obstruction or damage will usually require anastomotic revision or temporary percutaneous nephrostomy tube placement. The clinical picture of an unrecognized ureteral injury depends on the extent of the injury and may include nonspecific signs and symptoms such as nausea, fever, or abdominal pain. If the ureter is inadvertently ligated, the corresponding kidney will be obstructed, leading to hydronephrosis, flank pain, decreased urine output, and a rise in the serum creatinine. If the ureter is divided or an injury leads to ureteral perforation, urinary ascites will ensue, resulting in abdominal pain, peritonitis, azotemia from peritoneal absorption of urine, or an increase in fluid output from the surgical drain. If a urine leak is suspected, the fluid from the drain may be analyzed for creatinine. A 2-fold or greater increase in the drain creatinine as compared with serum creatinine may indicate that a urine leak is present.
Bladder injuries are rare in RRP and RPP and occur almost exclusively in LRP during the dissection of the retrovesical space to gain access to the seminal vesicles or during dissection of the retropubic space during a transperitoneal approach. In their series of 567 patients, Guillonneau et al reported 9 bladder injuries, all of which occurred during dissection of the retropubic space.48 These were identified intraoperatively and repaired without sequelae. Bladder injury during retropubic dissection is a particular risk if the patient has undergone a previous laparoscopic prosthetic mesh inguinal herniorrhaphy.49
Deep venous thrombosis and pulmonary embolus are infrequent but serious complications of RP. Perioperative prophylaxis with low-molecular weight heparin and/or pneumatic compression stockings, as well as early postoperative ambulation, have decreased the frequency of these complications even further. Early series of RRP reported the rate of these complications to be as high as 5%.50 Current LRP series report the frequency of these complications at 0% to 1%. In cases where thromboembolic events were reported, patients were usually confined to bed for prolonged periods of time, usually because of other complications (bleeding, peritonitis, anastomotic leak).31
Mortality after RP is low and has been estimated at 0.5% in recent series.51 It seems likely that the implementation of routine prostate-specific antigen testing has led to prostate cancer diagnoses in younger and healthier men who would be less prone to having serious cardiovascular complications. Mortality rates seem to be directly correlated to patient classification by the American Society of Anesthesiologists system.52
Urine leak into the pelvis (or the peritoneum, depending on surgical approach) from the urethrovesical anastomosis can be observed as an early or late complication. Although it is seen in up to 13%12 of patients after LRP, it is less common in RRP and RPP. The best method to prevent a leak from the anastomosis is to ensure intravesical positioning of the bladder catheter and to test the anastomosis for watertightness with saline irrigation intraoperatively. If a leak is detected postoperatively, this should be managed by continuing the closed suction drain and bladder drainage until the leak closes.
Bladder neck contracture is usually a late complication of RP and has been reported in approximately 0.5% to 2% of LRP patients and 0.5% to 17.5% of RRP patients.53 Prior transurethral resection of the prostate, excessive intraoperative blood loss, and urinary extravasation at the anastomotic site seem to be risk factors for bladder neck contracture.54 Most anastomotic strictures require cold-knife incision and/or periodic dilation to maintain adequate urine flow.
Perhaps the 2 most feared complications of RP from a patient's perspective are urinary complications and impotence. One difficulty in assessing these complications is that there are no precise definitions of incontinence or impotence in the literature. Furthermore, centers have obtained their outcomes data by widely divergent methods, including questionnaires, telephone interviews, or surgeon assessment. Lastly, continence and potency rates are improved when the patient population is highly selected (younger and with fewer comorbidities).
Urinary incontinence can be a devastating complication following prostatectomy. Given the difficulty in measuring this clinical outcome, however, continence results in the literature vary widely. Most centers with a high-volume experience in this procedure report continence rates between 80% and 95% (Table 1).
Several studies have examined the factors associated with improved postoperative continence.61–63 In multivariate analyses of pre- and postoperative factors, significant factors that improved chances of postoperative continence were younger age, preservation of both neurovascular bundles, absence of an anastomotic stricture, preservation of functional urethral length, eversion of the bladder neck, and a smaller prostate volume.61,64–68 If incontinence is present, pelvic floor exercise, as well as biofeedback, may be beneficial.69 Improvement in urinary continence may occur 1 or even 2 years following surgery. Therefore, invasive treatments for incontinence should be delayed for at least 1 year after prostatectomy.70 Once incontinence is noted to persist, several modalities, including cystoscopy, uroflow, and urodynamics, can be implemented to diagnose the cause and exclude potentially treatable etiologies. Final treatment decisions can then be based on findings from these studies. Surgical and conservative options for postprostatectomy incontinence are covered elsewhere.71,72
Before the development of an anatomic approach to RP, virtually all patients developed impotence following RP. The realization that impotence arose from damage to an anatomically distinct network of autonomic nerves to the corpora cavernosa led to modifications in surgical technique, with vastly improved potency outcomes.11 In 1991, Quinlan evaluated the recovery of sexual function in 600 consecutive men.73 Of the 503 patients who were potent preoperatively and followed up for a minimum of 18 months, 68% were potent postoperatively. Three factors were identified that correlated with return of sexual function: younger age, lower clinical and pathologic stage, and surgical technique (preservation or excision of the neurovascular bundle). Of note, patients who are immediately impotent after surgery may develop erections adequate for intercourse up to 24 to 48 months after surgery.74 Furthermore, with the use of phosphodiasterase inhibitors such as sildenafil citrate, up to 80% of men who had no erections after RP will eventually recover.75 In a questionnaire study, Walsh et al found that the recovery of sexual function occurred gradually after surgery, with 38% of patients potent at 3 months, 54% at 6 months, 73% at 12 months, and 86% at 18 months.76 The recovery of sexual function also correlated with the age of the patient at the time of surgery and was 100% in men aged 30 to 39 years, 88% in men aged 40 to 49 years, 90% in men aged 50 to 59 years, and 75% in men aged 60 to 67 years. These observations, they concluded, were secondary to the fact that in this era of prostate-specific antigen screening, more men are presenting at a younger age with organ-confined tumors that are amenable to nerve-sparing surgery.
Here we present the published data for both of these parameters in contemporary series of RRP and LRP.8,55–60,76–80 Table 1 shows urinary continence rates for RRP and LRP, defined as no need for any pads or “protection.” Table 2 shows the sexual potency rates. As can be seen, the rates of potency and continence are comparable for both techniques, especially when the mean patient age is considered. Essentially, postoperative results regarding continence and sexual potency are multifactorial and depend on preoperative function, coexisting disease, and social habits (tobacco and drug use).
The fundamental principles of meticulous tissue handling and avoiding electrocautery during the neurovascular dissection hold true for both RRP and LRP and should minimize injury to these structures, hopefully resulting in optimal potency and continence rates.
Radiation administration is an effective means of prostate cancer treatment that provides cure rates comparable with those of RP. While treatment outcomes may be similar, radiation therapy possesses its own unique set of side effects. Additionally, the side-effect profiles differ depending on the method of radiation administration, namely external beam radiation therapy (EBRT) or interstitial brachytherapy (IB or radioactive seed implantation). While most published assessments of morbidity have used physician reports of significant side effects, more recent studies have focused on patient-driven indices of morbidity. Their analysis has been given greater power by the recent use of health-related quality-of-life (HRQOL) tools. No longer are these side effects viewed in abstraction, but rather they are viewed in the context of the individual whom they affect, painting a clearer picture of the nature and consequences of radiation-associated morbidity.
This section focuses on the side-effect profiles of EBRT and IB as separate entities and concludes with recent quality-of-life analyses relating to these modalities. Medical innovation continues to improve the overall quality and accuracy of radiation treatment. Mature data focuses its lens on therapies that have since been refined and improved. With this in mind, it is hoped that these advances will lessen the morbidity experienced by men treated today.
EBRT for prostate cancer consists of the administration of ionizing radiation produced by a linear accelerator. The head of the accelerator rotates around the patient, allowing the radiation beam multiple angles of entry. The resultant effect is an intersection of multiple radiation beams at a specific site within the body. Planning of therapy begins with a CT scan that allows the physician to map out the prostate, seminal vesicles, and draining lymph nodes and to construct a 3D anatomic model. This map guides the planner in the best beam arrangement to provide adequate dose to the sites of disease while attempting to minimize dose to adjacent normal structures. Men with early-stage prostate cancer are treated to the entire prostate and the caudal portion of the seminal vesicles. Men with more advanced disease often receive radiation to the draining pelvic lymph nodes, at the discretion of the treating physician. Daily prostate position is usually ascertained by transabdominal ultrasound or by plain x-rays to identify implanted, inert, fiducial markers. Accounting for daily position allows for the use of tighter radiation fields and reduced normal tissue volumes within the high-dose area.
In order to adequately treat the prostate, adjacent normal structures are, by necessity, irradiated. The bladder neck (superior), penile bulb (inferior), and the anterior rectal wall (posterior) all receive significant doses of radiation (Figure 1). In addition, the prostatic urethra and neurovascular bundles lie within the treatment field. Finally, if pelvic nodes are irradiated, the bladder, rectum, sigmoid colon, and small bowel all receive additional doses. The anatomy of the male pelvis, therefore, dictates morbidity, namely a decline of sexual function, rectal urgency and bleeding, and obstructive and irritative voiding symptoms.
The majority of the acute urinary dysfunction caused by EBRT relates to inflammation and mucosal loss at the bladder neck and within the prostate and prostatic urethra. Symptoms usually begin 2 to 3 weeks into therapy, when the mucosa first becomes denuded, and continue for several weeks until re-epithelialization is complete (Figure 2A). Both irritative and obstructive urinary symptoms may occur, with a tendency toward the latter in men with larger prostates. Pinkawa et al recently addressed acute urinary toxicity in 204 men treated to >70 Gy with external beam irradiation with special emphasis on pretreatment prostate volume.81 Side effects were measured at completion of treatment, as well as at 2 and 12 months afterward. One-third of men reported dysuria, and 37% reported obstructive symptoms at completion of treatment. By 2 months post-treatment, these symptoms had returned to baseline. Both dysuria and obstructive symptoms were more common in the large prostate group (>43 cm3). Obstructive and irritative urinary symptoms during and after radiation are often effectively managed with alpha blockers, such as tamsulosin or terazosin, or by anticholinergics.82 The latter must be used with caution in men with pre-existing benign prostatic hypertrophy because of a risk of acute urinary retention.
Months or years after external radiation, late sequelae may develop. These are the result of changes in the small vessels of the irradiated tissues that lead to chronic hypoxia, mucosal thinning, and aberrant vessel development (telangiectasia) (Figure 2B). Patients may experience painless hematuria, a common though rarely serious event, or a syndrome similar to chronic interstitial cystitis, with frequency, dysuria, and even bladder contracture.83 The reported rates of urethral stricture are below 10% but are higher in men who have had prior transurethral resection.84
Irradiation of the anterior rectal wall is the cause of gastrointestinal sequelae in men with prostate cancer. During treatment, rectal urgency and tenesmus may occur. In later years, by similar mechanisms to the previously mentioned late bladder morbidity, men may experience rectal bleeding or, rarely, ulceration. Men receiving radiation to the pelvic lymph nodes have a larger volume of bowel irradiated and, consequently, an increased rate of side effects with a different profile. Small bowel issues such as cramping, diarrhea, and late adhesions are more likely to occur. Crook et al queried 192 patients treated to the prostate (+/−) iliac nodes a mean of 33 months after treatment completion.85 Two-thirds of these patients noted either no or mild gastrointestinal changes. The remaining third with moderate or severe dysfunction reported hematochezia (9%), rectal urgency (20%), or the need for transfusion or laser surgery (4%). The majority of mild to moderate symptoms are treated effectively with simple dietary changes, especially fiber, or by the use of hydrocortisone suppositories or foam. For the rare patient with persistent bleeding despite conservative medical management, the abnormal vessels can be treated electrosurgically by argon plasma coagulation via an endoscope to prevent further episodes. Late rectal complications peak in number and severity in the first 3 years, thereafter often resolving slowly.
Radiation to both the neurovascular bundles and penile bulb lead to decreased potency in treated men compared with age-matched controls. There is thought to be a 3-fold pathogenic mechanism: penile arterial insufficiency, venous insufficiency at the level of the penile bulb with reduced blood trapping, and direct nerve damage within the neurovascular bundle. Patients who enter treatment with partial potency, diabetes, or who receive even a brief course of neoadjuvant or concomitant ADT are at markedly increased risk of treatment-induced impotence. Potosky et al followed 435 men treated with EBRT in 1994/1995. Of these men, 50.3% and 63.5% were unable to obtain erections sufficient for intercourse 2 and 5 years after treatment, respectively.86 Phosphodiesterase inhibitors have been shown to improve function in up to two-thirds of patients with erectile dysfunction after EBRT.87
A rare but serious complication of irradiating normal tissues is the induction of second cancers. Brenner et al have looked at all patients with prostate cancer in the Surveillance, Epidemiology, and End Results (SEER) database treated by radiation between 1977 and 1993 and found a 1% additional absolute risk of cancer 10 or more years later.88 These were mainly bladder and rectal cancers (Figure 2C). While the risk is almost certainly lower with contemporary techniques, it will not be reduced to zero and remains a consideration when treating younger men.
In the 1970s and 1980s, the majority of external treatments were delivered using large fields and 2D-planning techniques treating significant volumes of normal tissue. In the 1990s, CT information improved the therapeutic ratio, and more recently, intensity-modulated radiation therapy (IMRT) has added an additional degree of precision. IMRT allows the physician to control the intensity of radiation produced by each individual beam, allowing for even greater conformality of dose to tumor. Several studies have shown a decreased rectal dose with IMRT compared with the 3D conformal technique. As expected, an associated decrease in chronic gastrointestinal morbidity was also noted.89
Proton-beam therapy has recently gained popularity as an EBRT modality. Based on their physical characteristics, protons also offer the potential advantage of reducing morbidity while providing equivalent levels of cure. Both IMRT and proton-beam therapy may reduce bladder and rectal morbidity but are unlikely to reduce the rates of erectile impotence since the neurovascular bundles running so close to the prostate remain within the high-dose volume. If these techniques are used to deliver increased radiation doses, the potency rates may even decline further.
IB consists of the introduction of radioactive sources (“seeds”) into the prostate itself. These seeds emit ionizing radiation, providing high doses of radiation to the tumor and surrounding structures. Similar to EBRT, treatment of the prostate necessitates irradiation of the penile bulb, neurovascular bundles, anterior rectal wall, prostatic urethra, and bladder neck. Classically, low-dose–rate (LDR) emitters such as iodine and palladium have been used. Recently, temporary high-dose–rate (HDR) brachytherapy with iridium has seen increasing use.
Brachytherapy procedures begin with a volume study. A transrectal ultrasound probe is used to visualize and create a 3D map of the prostate. With this information, radioactive seed number, location, and activity can be calculated using a planning computer. Once a plan is in place, seeds are loaded into 18-gauge needles and inserted into the prostate using a perineal approach under general anesthesia. Transrectal ultrasound is used to visualize the prostate and determine correct needle placement during the procedure. Seeds can be placed homogenously throughout the prostate or can be concentrated in the prostate periphery. Peripheral loading prevents the extremely high central doses and damage to the prostatic urethra caused by a homogenous plan. Peripheral loading, however, increases the number of sources in close proximity to bowel and bladder, increasing radiation dose to these tissues. Due to these considerations, a modified peripheral loading technique in which peripheral dose can be decreased by placement of a limited number of centrally located sources has gained favor.
Urinary issues are the most common side effects of seed implantation. A study of 693 consecutive patients at Memorial Sloan Kettering from 1992 to 1997 reported 37% Grade 1 urinary toxicity, 41% Grade 2 toxicity, and 2.2% Grade 3 toxicity within 60 days of seed placement, by the Radiation Therapy Oncology Group toxicity scale.90 There is a biphasic pattern to these effects. The first phase occurs within 24 hours of the procedure due to the immediate trauma of needle insertion, and the second begins 2 to 3 weeks after seed introduction when a radiation-induced inflammatory prostatitis becomes evident. Irritative and obstructive symptoms, namely frequency, urgency, dysuria, incomplete emptying, and weak stream, peak about 1 month after seed implantation and generally completely resolve by 1 year.91 The vast majority of these symptoms are mild in nature and can be treated effectively with alpha blockers.92 Preprocedure gland size and American Urological Association benign prostatic hypertrophy symptom score effectively predict the men at higher risk of significant urinary side effects.93 Less common side effects include hematuria and urethral stricture.
Urinary retention requiring catheterization can occur both directly following as well as 2 to 3 weeks postprocedure. The chance of retention is directly related to prostate gland size, with glands >60 cm3 conferring a markedly increased risk.94 A postoperative course of corticosteroids decreases the rate of urinary retention.90 It is of note that men undergoing a transurethral resection of the prostate either before or following brachytherapy have a significant risk of a relatively unique complication, superficial urethral necrosis (Figure 3A). The pathogenesis of this complication is unclear and usually leads to incontinence.
While far less common than urinary sequelae, rectal irritation, urgency, bleeding, and loose stool are all possible side effects of brachytherapy. Shah and Ennis evaluated postimplant rectal toxicity in a cohort of 135 patients, with a median follow up of 41 months. Diarrhea was noted in 17.5% of patients in the 6 months after treatment, although only 0.8% met Grade 2 criteria (by National Cancer Institute Common Toxicity grading). In addition, urgency, proctitis, incontinence, and bleeding were noted in 5% to 10% of patients. Late toxicity (more than 6 months postprocedure) consists of these same symptoms, although with decreased frequency. Radiation proctitis is directly related to the amount of rectum receiving significant radiation dose. Specifically, increased late toxicity was noted when greater than 25% of the rectum received greater than 25% of the prescribed dose.95 A recent study promotes injection of hyaluronic acid as a spacer between prostate and rectal wall to reduce rectal dose and hopefully mitigate side effects.96
Diarrhea can be effectively managed with antidiarrheal agents such as loperamide (Imodium), while proctitis and urgency are often effectively treated with dietary modification and/or psyllium (Metamucil) to add increased bulk. For those patients with significant rectal irritation, cramping, and tenesmus, steroid suppositories may provide relief.
While occurring in less than 1% of patients, formation of a rectal fistula is a serious complication (Figure 3B). Men who are at higher risk for this dreaded complication include those who receive combined EBRT and IB, those with vascular disease, those with poorly controlled diabetes, and those with inflammatory bowel disease. Postimplantation biopsy also increases this risk.
Brachytherapy carries a risk of sexual dysfunction similar to EBRT. Merrick et al studied 128 potent men who received seed implants between 2001 and 2003. The actuarial rate of potency preservation was 51% at 3 years. The median time to loss of potency was 5.4 months after the procedure.97 Dose to the proximal crura and marginal potency pretreatment were statistically significant predictors of treatment-induced impotence. Potters et al noted a 5-year potency rate of 76% for those receiving seeds as monotherapy. The addition of EBRT or ADT markedly decreased potency in this study group.98 In this study, 62% of impotent patients were able to achieve erections capable of intercourse with the addition of sildenafil. Notably, this percentage was >80% when men receiving ADT were excluded.
HDR IB has increased in use over the last several years. As with standard LDR brachytherapy, HDR brachytherapy is administered by placement of radioactive sources within the prostate using a perineal approach. In contrast to LDR, HDR brachytherapy is administered in 2 or more large fractions over a period of 24 to 48 hours and requires hospitalization during administration. HDR is traditionally used in combination with EBRT for men with advanced local disease.
Limited data are available comparing HDR brachytherapy with other radiotherapy options. A single study compared standard LDR brachytherapy with HDR monotherapy in 149 men with early-stage prostate cancer.99 In this study, HDR resulted in decreased dysuria (36% versus 67%), urinary urgency (54% versus 92%), and rectal pain (6% versus 20%). There was an increased risk of urethral stricture with HDR (8% versus 3%).
Recent analysis of patient outcomes has shifted from simply a list of the prevalence and incidence of various side effects to a more “holistic” quality-of-life measurement. HRQOL measures the interplay between the sequelae of an intervention and the patient's expectations, tolerances, personal and professional relationships, satisfaction, and overall happiness.100
HRQOL is determined using standardized question sets directly administered to patients. Several validated disease-specific questionnaires have been generated for prostate cancer that address the specific influence of bowel, bladder, and sexual function on overall quality of life, including the Expanded Prostate Cancer Index Composite101 and the Functional Assessment of Cancer Therapy-Prostate instrument.99 Several recent studies have used these questionnaires to compare HRQOL following various treatment modalities.
Lee et al used the Functional Assessment of Cancer Therapy-Prostate instrument questionnaire to assess HRQOL at set intervals during the first year after radiotherapy treatment.102 A significant decrease in HRQOL was noted among IB patients at 1 and 3 months post-treatment. No significant differences compared with pretreatment were noted in either the EBRT group at any point or the IB group 1 year after therapy.
Clark et al looked at HRQOL in 130 patients who received EBRT and 16 patients who received brachytherapy 12 to 48 months after treatment completion.103 Significant urinary obstructive/irritative, bowel, and sexual dysfunction were noted compared with controls. There was not a significant increase in self-reported urinary incontinence compared with controls. These findings correlated with a statistically significant decrease in urinary control, sexual intimacy, and sexual confidence on quality-of-life analysis. Marital affection and masculine self-esteem were not lessened.
Wei et al measured HRQOL among 902 subjects treated with RP, EBRT (via a 3D conformal technique), or IB at the University of Michigan with a median follow up of 2.6 years.104 An additional 114 male volunteers served as age-matched controls. General HRQOL did not differ amongst any treatment group and age-matched controls. IB patients had worse sexual, bowel, and urinary irritative and obstructive quality of life than controls. EBRT patients had worse bowel and sexual quality of life than controls, but comparable urinary quality of life. Comparison of IB and EBRT revealed increased incontinence and slightly worse bowel quality of life in the IB cohort compared with EBRT.
Miller et al re-evaluated this patient cohort at a median of 6.2 years after treatment.105 3D conformal EBRT patients continued to have poorer bowel and sexual HRQOL than the control group. IB patients continued to have poorer bowel, urinary, and sexual HRQOL compared with controls. Notably, urinary irritative HRQOL and bowel HRQOL improved markedly in IB patients in the study interval, although both were still substantially worse than the control group.
Provocatively, urinary incontinence HRQOL, measured as frequent urinary dribbling or pad requirements, worsened in both the EBRT and IB groups during the study interval while remaining unchanged in the control population. Furthermore, there was a decreased sexual HRQOL in the EBRT group, although this was mirrored by a similar decline in the control group, suggesting an age-related rather than treatment-related phenomenon.
The number of prostate cancer survivors in the United States is estimated at 2 million, and approximately one-third of these men are currently receiving ADT. In addition to a role in the adjuvant treatment of early, localized prostate cancer, ADT represents the primary treatment for recurrent prostate cancer. Once ADT is initiated for recurrent prostate cancer, therapy typically continues until the time of death, a period that may extend over many years. A singularly effective therapy in treating prostate cancer, ADT is increasingly recognized to have undesirable physiologic effects that may result in important long-term adverse consequences. Awareness of the potential adverse effects of ADT and the overall risk/benefit ratio is important in determining the suitability of treatment in individual patients.
ADT may be accomplished by either surgical or chemical castration. GnRH (gonadotropin-releasing hormone) agonists are the most commonly used agents for this purpose and effectively result in hypogonadism with reduction in serum testosterone levels of >95% and in estrogen levels of >80%. The adverse effects of ADT are due to hypogonadism and include vasomotor flushing, loss of libido, decreased bone density, increased fat mass, and decreased muscle mass.106 Additionally, long-term ADT is associated with an increased risk of diabetes and cardiovascular disease.107
Most men treated with ADT will experience vasomotor flushing, or hot flashes, which may have substantial impact on quality of life in some men. Hot flashes are described as unpredictable episodes of intense warmth in the upper part of the body and face, accompanied at times by diaphoresis. A number of “natural remedies” have been touted to treat hot flashes, including acupuncture, black cohosh, flax seed, or soy products, but none is demonstrated to help in other than anecdotal instances.
Transdermal estrogen and megestrol acetate have been shown to reduce hot flashes, but with adverse consequences, including breast swelling and nipple tenderness with estrogens and weight gain with megestrol.108,109 Selective serotonin uptake inhibitors are effective in women with breast cancer and menopausal hot flashes; although no randomized trials have been carried out in men, venlafaxine and paroxetine appear to be occasionally effective in small studies of men with hot flashes.110,111
Androgens promote erythropoiesis by increasing erythopoietin production and by direct activation of erythrocyte progenitors.112 GnRH agonists significantly decrease hemoglobin concentrations in men with prostate cancer.113–116 The median decrease in hemoglobin concentrations is about 1 g/dL but sufficient to cause anemia in most men.115,116 Treatment-related anemia is usually mild and not associated with symptoms. It is characteristically normochromic and normocytic. Erythropoietin increases hemoglobin concentrations in men receiving GnRH agonists for prostate cancer,115 although treatment for anemia in this setting is rarely necessary.
Fatigue is a common and important adverse effect of ADT. Approximately two-thirds of men report increases in fatigue after treatment with a GnRH agonist.117 Changes in body composition, particularly decreased lean body mass, may contribute to treatment-related fatigue. Anemia may also contribute to treatment-related fatigue.
Gynecomastia is defined as benign proliferation of the glandular subareolar breast tissue. Mastodynia refers to breast/nipple tenderness. The incidence of gynecomastia and/or mastodynia varies with the type and duration of ADT. About 10% to 15% of men develop gynecomastia after bilateral orchiectomies or treatment with a GnRH agonist.118 In contrast, the majority of men receiving monotherapy with an antiandrogen develop gynecomastia.119 Prophylactic breast irradiation appears the most effective strategy to prevent or mitigate gynecomastia; treatment after development of gynecomastia may improve pain but does not improve enlargement.120,121 Tamoxifen is the most effective medical therapy for gynecomastia and/or mastodynia.122,123 Breast reduction surgery may benefit the occasional man with severe breast symptoms that are refractory to medical treatment.
Several prospective studies have demonstrated that ADT results in immediate and sustained decrease in bone mineral density (BMD) in men with prostate cancer.124–129 The decrease in BMD continues at an average rate of 2% to 3% per year during treatment, and the risk of fracture and development of osteoporosis therefore appears to increase steadily with duration of therapy.
The mechanism of BMD decline may relate to an increase in bone turnover due to ADT. Bone turnover markers measured in serum and urine demonstrate increased activity of both osteoblasts and osteoclasts and reach a plateau after 6 months of ADT.125,127 Changes in sensitivity of bone to parathyroid hormone might also contribute to increased osteoclast activation and decreased BMD.130
Osteoporosis is common in men, with an estimated prevalence of more than 2 million men in the United States.131 Hypogonadism may be the most common cause of acquired osteoporosis in men and together with alcohol abuse and chronic glucocorticoid therapy accounts for one-half of all cases of male osteoporosis.132 The decreased BMD and increased risk of osteoporosis engendered by ADT in men with prostate cancer is now firmly linked to an increased fracture risk.133–135 In one claims-based analysis, for example, men with prostate cancer who were receiving GnRH agonists were 1.4 times as likely to develop fractures as men with prostate cancer who had not received GnRH agonists.133
Daily supplementation of calcium and vitamin D is recommended by the National Institute of Health at doses of 1200 to 1500 milligrams/day and 400 IU/day, respectively. Supplementation with calcium and vitamin D modestly decreases fracture incidence in men and women over age 65 years.136 However, this is not sufficient to prevent bone loss in men treated with ADT.127
The increased risks of osteoporosis and fractures in men with prostate cancer receiving ADT have led to randomized controlled trials aimed at preventing or ameliorating these risks. Bisphosphonates, including pamidronate and zoledronic acid (ZA), are effective at preventing ADT-related BMD loss.127,129,137 In a study that treated 106 men receiving ADT for nonmetastatic prostate cancer with ZA versus placebo, ZA administered at 4 mg every 12 weeks significantly increased BMD in the hip and lumbar spine by 3.9% and 7.3%, respectively.129 In another randomized study, a single infusion of ZA resulted in significantly increased BMD in the hip and spine after 1 year.138 The differences in BMD between the men treated with ZA versus placebo were similar in the 2 studies, suggesting that annual infusion of ZA might be sufficient to prevent treatment-related loss of BMD.
Three ongoing randomized controlled trials are assessing the impact of medical therapy with denosumab, toremifene, or ZA on fracture prevention:
Currently, we recommend routine use of supplemental calcium and vitamin D in all men treated with ADT. Men undergoing long-term ADT for nonmetastatic prostate cancer should have assessment of fracture risk by history, laboratory testing, and measurement of BMD. For men at greatest fracture risk, selective use of drug therapy should be considered.
ADT is accompanied by prompt and often marked changes in body composition.
Quantitative analysis of men beginning GnRH-agonist therapy has shown an increase in fat mass of 9.4% to 11% in 1 year, with a concurrent decrease in lean body mass of 2.7% to 3.8%.116,141 The increase in fat mass is observed in subcutaneous rather than intra-abdominal fat. Two other studies in men with nonmetastatic prostate cancer found an increase in mean fat mass of 8.5% or 4.3% within 3 months of starting ADT, suggesting that this effect may be important even for men treated with short courses of ADT.142,143 Because of the association between increased weight, fat mass, and insulin resistance, further studies have assessed the relationship between ADT and insulin resistance.
Treatment-related changes in body composition are accompanied by adverse metabolic effects. GnRH agonists increase serum total cholesterol, low-density lipoprotein cholesterol, and triglycerides.116,144 In a prospective 12-month study, for example, GnRH agonists increased serum total cholesterol, low-density lipoprotein cholesterol, and triglycerides by 9.0%, 7.3%, and 26.5%, respectively.142 GnRH agonists increase fasting plasma insulin level, a surrogate for insulin resistance.142,145 In a prospective study of non-diabetic men with prostate cancer initiating GnRH-agonist therapy, fasting plasma insulin levels increased by 26%, and the whole-body insulin sensitivity index decreased by 11%.146
The term “metabolic syndrome” refers to a clustering of specific cardiovascular disease risk factors whose pathophysiology appears related to insulin resistance.147 The National Cholesterol Education Program's Adult Treatment Panel (ATP III) and World Health Organization have defined the metabolic syndrome using distinct but related criteria. A recent cross-sectional study reported a higher prevalence of the metabolic syndrome (as defined by the ATP III) in 18 men receiving a GnRH agonist than in age-matched control groups of untreated men with prostate cancer and men without prostate cancer.148 Men receiving GnRH-agonist therapy had greater prevalence of increased abdominal girth, elevated triglycerides, and elevated fasting plasma glucose—consistent with results of prospective studies of GnRH-agonist treatment. In contrast with the metabolic syndrome, however, prospective studies have shown that GnRH agonists preferentially increase subcutaneous rather than visceral abdominal fat and increase rather than decrease high-density lipoprotein cholesterol.149 In addition, GnRH agonists increase serum adiponectin levels in men with prostate cancer, whereas the metabolic syndrome is associated with low adiponectin levels. Taken together, these observations suggest that GnRH agonists cause a pattern of metabolic changes that is distinct from the classically defined metabolic syndrome.
Diabetes and cardiovascular disease are leading causes of death in men. The adverse treatment-related changes in weight, body composition, lipids, and insulin sensitivity raise the possibility that ADT may increase the risk of these medical conditions. To evaluate the relationship between ADT and risk for incident diabetes and cardiovascular disease, Keating and colleagues conducted a large population-based study using the SEER-Medicare database.107
This landmark study included 73,196 men diagnosed with local or locoregional prostate cancer between 1992 and 1999 with follow up through 2001. Of the total population, one-third of men were treated with ADT during the study period. The analysis was adjusted for both patient and tumor characteristics. After adjusting for a variety of covariates, ADT with a GnRH agonist was associated with a significantly greater risk of incident diabetes (adjusted hazard ratio 1.42, P <.001), coronary heart disease (adjusted hazard ratio 1.16, P <.001), and admission for myocardial infarction (adjusted hazard ratio 1.1142, P <.03). A subsequent study using SEER-Medicare data confirmed the link between ADT and incident cardiovascular disease.150
Death rates from prostate cancer have steadily declined in recent years due to earlier diagnosis and treatment. The 5-year relative survival from prostate cancer is 98%.1 Improvements in cancer control, however, have been accompanied by a greater burden of treatment for prostate cancer survivors. Recognition of the potential adverse effects of surgery, radiation therapy, and hormone therapy and effective strategies to reduce treatment-related morbidity are necessary to decrease both death and suffering from prostate cancer.
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Disclosures: Dr. Zeitman receives an honorarium for serving as a speaker for Ismar Healthcare. Dr. Smith serves as a consultant for Amgen, Novartis Oncology, Merck, and GTx. No other potential conflict of interest relevant to this article was reported.
M. Dror Michaelson, Assistant Professor of Medicine, Division of Hematology/Oncology, Massachusetts General Hospital, Boston, MA.
Shane E. Cotter, Resident, Harvard Radiation Oncology Program, Boston, MA.
Patricio C. Gargollo, Instructor in Surgery, Harvard Medical School, Department of Urology, Massachusetts General Hospital, Boston, MA.
Anthony L. Zietman, Professor of Radiation Oncology, Jenot and William Shipley, Harvard Medical School, Massachusetts General Hospital, Boston, MA.
Douglas M. Dahl, Associate in Urology, Massachusetts General Hospital; and Assistant Professor of Surgery (Urology), Harvard Medical School, Boston, MA.
Matthew R. Smith, Associate Professor of Medicine; and Director of Genitourinary Medical Oncology, Massachusetts General Hospital, Boston, MA.