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Benign Prostatic Hyperplasia: Current Treatment Strategies


Benign prostatic hyperplasia (BPH)-histologically defined as stromal and epithelial hyperplasia beginning in the periurethral transitional zone of the prostate-affects up to 80% of 80-year-old men.[1,2] With progressive prostatic enlargement, bladder outlet obstruction can result. Although the exact mechanism is unknown, lower urinary tract symptoms (LUTS) can signal progressive BPH.


BPH: When to Treat and How

Elevated PSA Levels Raise Questions

Benign prostatic hyperplasia (BPH)-histologically defined as stromal and epithelial hyperplasia beginning in the periurethral transitional zone of the prostate-affects up to 80% of 80-year-old men.1,2 With progressive prostatic enlargement, bladder outlet obstruction can result. Although the exact mechanism is unknown, lower urinary tract symptoms (LUTS) can signal progressive BPH.

Here we review current therapeutic options for BPH, including active surveillance; medical therapy (α-blockers, 5α-reductase inhibitors, anticholinergics, phosphodiesterase 5 [PDE-5] inhibitors, and phytotherapy); minimally invasive therapies (MITs), such as transurethral microwave therapy (TUMT) and transurethral needle ablation (TUNA); laser therapies; and botulinum toxin injection.


This approach is appropriate for patients with minimal LUTS (American Urological Association Symptom Score [AUA SS] of 7 or lower) or those with only mild to moderate symptoms (AUA SS of 8). Active surveillance is distinguished from watchful waiting in that patients are monitored annually for disease progression with a history, physical examination, AUA SS, and a bother score.2 If symptoms or bother scores worsen, or if clinical sequelae such as retention or infection develop, treatment is warranted.


Before the late 1970s, the only treatment for patients with BPH was surgical resection, such as open prostatectomy or transurethral resection of the prostate (TURP). In 1978, Caine and colleagues3 reported that phenoxybenzamine, a nonselective α-blocker, was an effective treatment for patients with BPH. This seminal observation formed the basis for substantial research, with the result that α-blockers are currently the initial treatment for most men with symptomatic BPH.

α-Blockers. α-Blockers work by antagonizing the α-adrenergic receptors on the smooth muscle in the prostate.4 The α1a is the predominant receptor in the human prostate.5

Currently available α-blockers include doxazosin, terazosin, alfuzosin, and tamsulosin. They are long acting (once-daily dosing) and α1a-selective. A meta-analysis by Djavan and Marberger6 demonstrated a comparable magnitude of improvement in both AUA SS and urinary flow. Tamsulosin and alfuzosin had adverseeffect profiles comparable to those of placebo. Patients treated with terazosin and doxazosin, however, had a 4% to 10% greater dropout rate because of adverse effects than did patients receiving placebo. The adverse effects were typically dizziness, asthenia, somnolence, and headache.7,8

Ejaculatory dysfunction occurs more frequently with tamsulosin, but the increased frequency is not large enough to be consistently detected in comparative studies.9 Both doxazosin and terazosin require dose titration when treatment is initiated because of the potential for hypotension. Tamsulosin and alfuzosin do not.

The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) randomized patients with hypertension and other cardiac risk factors to receive either doxazosin or chlorthalidone, a diuretic. The doxazosin arm was terminated early because of a statistically significant (25%) higher incidence of major cardiovascular disease events, particularly congestive heart failure.10 Based on that study, the AUA 2003 Consensus Panel recommended that α-blockade should not be used as monotherapy for patients who have both BPH and hypertension and that a second agent should be used to manage the hypertension.2

The Medical Therapy of Prostatic Symptoms (MTOPS) study and the Alfuzosin Long-Term Efficacy and Safety Study (ALTESS) showed that α-blockers improve BPH symptoms and increase time to disease progression but do not prevent overall progression (defined as acute urinary retention and the need for invasive therapy).11,12 These studies also showed that α-blockers are less effective in men with large prostates and that dropout rates are relatively high after 3 to 4 years of therapy.

5α-Reductase inhibitors. 5α- Reductase inhibitors manage BPH by decreasing prostate volume. Dihydrotestosterone (DHT) is the primary androgen involved in prostatic growth. 5α-Reductase inhibitors (finasteride and dutasteride) prevent the conversion of testosterone to DHT by competitively inhibiting the enzyme 5α-reductase. There are 2 isoforms of 5α-reductase enzyme, types 1 and 2. Finasteride is a selective inhibitor of only the type 2 enzyme, whereas dutasteride inhibits types 1 and 2.

The 4-year Proscar Long-term Efficacy and Safety Study (PLESS) showed that finasteride increased flow rate, decreased AUA SS, reduced prostate volume by 32%, lowered the risk of acute urinary retention by 57%, and reduced the need for BPH-related surgery by 55%.13 The MTOPS study demonstrated that finasteride significantly reduced the risk of clinical progression of BPH by 34% compared with placebo and reduced the risk of acute urinary retention and the need for invasive therapy.11 The latter events (acute urinary retention and the need for invasive therapy) were not reduced in men receiving doxazosin monotherapy. The Prostate Cancer Prevention Trial (PCPT) showed that after 7 years, finasteride has an added benefit of decreasing the risk of prostate cancer by 24.8%.14

Dutasteride therapy had effects similar to those of finasteride. Roehrborn15 compared dutasteride with placebo and noted a decreased risk of acute urinary retention and BPHrelated surgery, a continuing improvement in flow rate and urinary symptoms, and a reduction in prostate volume. There was also a 50% reduction in the incidence of prostate cancer.16 The ongoing Reduction by Dutasteride in Prostate Cancer Events (REDUCE) trial is studying the effects of that drug on the incidence and progression of prostate cancer.16

Finasteride and dutasteride are well tolerated. Adverse effects (occurring in fewer than 1% of patients) include impotence, decreased libido, ejaculatory disorders, and gynecomastia. In most trials, men who experience adverse effects do so during the first year, with few additional subsequent adverse effects. 5α- Reductase inhibitors tend to have a greater effect in improving total symptom severity, frequency scores, and peak flow rates on prostates of larger volume.17

Combination therapy (an α- blocker plus a 5α-reductase inhibitor). The MTOPS study showed that management with a combination of finasteride and doxazosin reduced the clinical progression of BPH by 66% compared with treatment with finasteride or doxazosin alone (34% and 39%, respectively).11 While patients in all 3 active treatment arms (finasteride alone, doxazosin alone, and combination) showed a significant improvement in symptom scores compared with placebo, the combination arm was superior.

The Combination Therapy of Dutasteride and Tamsulosin Trial (CombAT) is a 4-year, multicenter, randomized, double-blind, parallel group study comparing the benefits of tamsulosin monotherapy, dutasteride monotherapy, and combination therapy in men older than 50 with an International Prostate Symptom Score (IPSS) greater than 12 and a prostate volume greater than 30 cc.18 Preliminary 2-year data show a statistically significant reduction in IPSS with combination therapy (6.2 point decrease) versus either dutasteride or tamsulosin monotherapy (4.9 and 4.3 point decrease, respectively). A statistically significant improvement in maximum urinary flow rate (Qmax) from baseline was also noted in the combination therapy arm (2.4 mL/s) compared with the dutasteride and tamsulosin monotherapy arms (1.9 and 0.90 mL/s improvement, respectively).

The MTOPS trial suggests that α-blockers manage symptoms with a relatively rapid onset of action but do not prevent disease progression. This observation gave rise to a strategy of initially combining an α-blocker and a 5α-reductase inhibitor for a short duration (3 to 6 months) followed by withdrawal of the α-blocker and continuation of 5α-reductase inhibitor monotherapy

The Symptom Management After Reducing Therapy (SMART-1) study examined such an approach using dutasteride and tamsulosin. Men were randomized to tamsulosin and dutasteride for 24 weeks, after which 50% discontinued tamsulosin.19 Most patients (84%), with an initial IPSS of less than 20, who were switched to monotherapy had sustained improvement in BPH symptoms. Therefore, most patients with mild to moderate BPH symptoms may benefit from an initial short duration of combination therapy followed by 5α-reductase monotherapy.

Combined α-blocker therapy and anticholinergic therapy. Patients with BPH often have concomitant irritative voiding symptoms because of an overactive bladder (OAB). Kaplan and colleagues20 performed a randomized, double-blind, placebo-controlled trial comparing tolterodine extended-release (ER), tamsulosin, tolterodine ER plus tamsulosin, and placebo in patients who had mild to moderate BPH and OAB. They found a statistically significant reduction in incontinence, frequency, and nocturia in the tolterodine ER plus tamsulosin group. These patients also had a statistically significant improvement in IPSS and quality of life.

The incidence of acute urinary retention requiring catheterization was low in all arms (less than 0.5%); patients treated with tolterodine ER and those treated with tolterodine ER plus tamsulosin had only a statistically insignificant increase in postvoid residual volume (PVR) from baseline (5 to 6 mL). Blake-James and associates,21 in a meta-analysis, observed similar results. Anticholinergic use did not significantly alter flow rates, and PVR was increased by only 11.6 mL (statistically insignificant). The rate of acute urinary retention was low (0.3%) and similar in all arms. Based on these data, anticholinergics appear to be safe to use in patients with both BPH and OAB.

PDE-5 inhibitors. Recent studies have shown that PDE-5 is present in human prostate and bladder tissue. This coupled with the observation that erectile function declines in men with increasing severity of LUTS prompted an initial evaluation of PDE-5 inhibitors as a treatment for LUTS. McVary and colleagues22 showed that both the IPSS and the BPH Impact Index were improved in men receiving tadalafil. Larger trials are needed to confirm these initial observations.

Phytotherapy. In 2002, more than 2.5 million adults reported using Serenoa repens (saw palmetto).23 In 1999, an estimated $1 billion was spent on phytotherapy for BPH, and spending has probably increased since that time.24 Despite the widespread use of plant extracts, recent studies do not support their effectiveness in the management of BPH. Bent and coworkers25 conducted a randomized, controlled, double-blind trial in 225 men comparing saw palmetto with placebo. They found no difference in change in AUA SS, Qmax, prostate size, quality of life, and adverse effects between the two groups. Until more data are produced, phytotherapy use remains controversial and cannot be currently recommended as a management option for BPH.


MITs include TUNA and TUMT. They gained widespread use because of their safety profile and because they can be performed as office procedures. Although these management options were initially judged as equivalent to TURP, recent studies do not confirm their long-term effectiveness. Both therapies have significantly higher re-treatment rates compared with those of TURP.

TUNA. Bouza and associates26 performed a meta-analysis on TUNA therapy, including 35 studies (mostly comparing TUNA and TURP). TUNA improved symptom index and quality- of-life scores by 50% to 60% from baseline and provided a 30% to 35% improvement in objective parameters (PVR and Qmax). Only 20% of patients experienced sexual adverse effects. The TUNA procedure had a 19% retreatment rate.

When comparing TUNA with TURP, short-term effectiveness appeared to be equivalent; however, within 1 year, there was a statistically significant difference in favor of TURP over TUNA. The re-treatment rate of men undergoing TUNA was 7.44 times higher than the rate of those undergoing TURP. However, TUNA has a significantly lower complication rate than TURP.

TUMT. Hoffman and colleagues27 performed a meta-analysis comparing TUMT with TURP. The pooled mean urinary symptom score decreased by 65% after TUMT and by 77% after TURP. Peak flows increased 70% after TUMT and 119% after TURP. Retrograde ejaculation (57% vs 22%), transfusion rate (5.7% vs 0%), and treatment of strictures (relative hazard, 9.76) were all significantly higher with TURP. However, re-treatment was significantly more common after TUMT (relative hazard, 10).

MITs, including TUNA and TUMT, appear to be safe procedures that provide short-term symptomatic relief. They are not as effective as TURP and have a higher re-treatment rate. Although MITs are not as durable as TURP, they are viable options in patients with significant operative risk. MITs may be an alternative to medical therapy in patients with mild to moderate voiding symptoms who do not want to take a pill every day.


TURP remains the gold standard of treatment for men with BPH. Absolute indications for TURP include refractory urinary retention, persistent prostatic bleeding (after other causes of hematuria have been excluded), bladder calculi, recurrent urinary tract infections, deterioration in renal function, and failure of medical therapy.2 Newer therapies, such as photoselective laser vaporization of the prostate (PVP), Holmium laser enucleation of the prostate (HoLEP), and Holmium laser ablation of the prostate (HoLAP), are currently being used widely and may replace TURP as the new gold standards of care.

PVP. This therapy uses the 80-watt potassium-titanyl-phosphate, or “green light laser,” that emits a 532-nm wavelength selectively absorbed by hemoglobin. The wavelength penetrates 2 to 4 mm and causes photoselective vaporization of the prostatic tissue. Because of vaporization and the shallow penetration, large-volume sloughing of the prostate does not occur. The effect of PVP is immediate.

Several articles have examined the safety and effectiveness of PVP among patients with large prostates (more than 60 g, with mean volume of 100 g),28 those receiving anticoagulation medication,29 and those with significant comorbidities.30,31 PVP can be used with normal saline and is not associated with transurethral resection (TUR) syndrome development even when large prostates are resected.32

In a nonrandomized trial, Bachmann and coworkers33 compared 37 patients undergoing TURP with 64 patients undergoing PVP, with 6-month follow-up. PVP patients had a shorter catheterization time (1.8 vs 3.0 days) but had a slightly higher recatheterization rate (7.8% vs 2.7%). The investigators noted similar 6-month improvements in symptom score and flow rate in both arms of the study.

Sarica and associates34 presented the largest series (240 patients) with a 1-year follow-up. Catheterization time averaged 12 hours, and hospitalization stays were all less than 24 hours. At 1 year, mean IPSS decreased from 22.6 to 3.7 (84%), and peak flow rate increased from 7.9 ± 2.7 mL/s to 27.9 ± 10.3 mL/s. Malek and colleagues35 reported durable improvements in symptom score, quality-of-life score, peak flow rates, and PVR up to 5 years. These studies reported minimal adverse effects, the most common of which was transient dysuria that lasted up to 14 days.

One drawback of PVP is the lack of tissue specimen; however, this seems to be less of an issue in the prostate-specific antigen era. Some urologists are bothered by the special glasses required to perform PVP (everything appears orange). Despite these disadvantages, PVP appears to be a safe and efficient alternative to traditional TURP, although long-term (more than 5 years) data are not yet available.

Holmium laser (HoLEP and HoLAP). The Holmium laser has a wavelength of 2140 nm that is strongly absorbed by water. The laser only penetrates 0.4 mm, resulting in precise tissue vaporization without deep coagulation or surrounding char effect. HoLEP involves transurethrally enucleating the individual lobes of the prostate with an end-firing Holmium laser and floating the enucleated lobes into the bladder. The prostate tissue is then removed with a transurethral mechanical morcellator.

Kuntz36 reviewed the use of HoLEP in more than 5000 patients. He reported that HoLEP can be used in prostates of all sizes (even more than 300 g) and in patients receiving anticoagulation medication. Operative times were longer with HoLEP than with TURP, but intraoperative blood loss was less, hospitalization time was shorter, catheterization times were less, and TUR syndrome did not occur.

In the reviewed studies, patients who underwent HoLEP had results- urinary improvement and relief of bladder outlet obstruction based on urodynamics-that were better than or equivalent to those for TURP. Westenberg and associates37 and Kuntz and coworkers38 reported durable results with HoLEP compared with TURP with 4-year and 3-year follow-up. HoLEP provides tissue for diagnosis; the other vaporization procedures do not. Despite these advantages of HoLEP, it is not performed widely, possibly because of its steep learning curve.

HoLAP was initially described in 1994 and has recently gained widespread use with its new 100-watt laser and side-firing arm. Although no long-term data are yet available, it seems to be an attractive treatment for patients with BPH. It has a short learning curve, and it results in minimal or no hospital stay, early catheter removal, and the ability to treat patients with significant medical comorbidities and those receiving anticoagulation medication. HoLAP results in less sloughing and decreased irritative voiding compared with PVP because of its shallower depth of penetration (0.4 mm vs 2 to 4 mm).

The 100-watt Holmium laser is a versatile tool for urologists; it can be used in the management of other conditions, including stones, strictures, and tumors.


Botulinum toxin type-A (BONTA), produced by the bacterium Clostridium botulinum, has recently gained interest for the management of symptomatic BPH. Botulinum toxin is injected into the prostate either transurethrally, transrectally, or transperineally with transrectal ultrasonographic guidance. Between 100 and 200 units of BONT-A are injected into both lobes of the prostate.

Oeconomou and associates39 recently published a review of the effects of BONT-A on BPH in animal models and the results of 10 clinical trials including 294 patients. Although the mechanism of action is unknown, BONT-A seems to produce apoptosis and atrophy of prostatic tissue in animal models. BONT-A may also have an effect on the dynamic component of BPH; it is effective in patients with small prostates (less than 30 g).

Although the reported studies have small patient numbers (the largest study included 52 patients), preliminary data appear promising, with improvements in symptom score, peak flows, quality of life, and reduction in prostatic volume. Durable results as long as 19 months have been reported. Caution is advised in using BONT-A to manage BPH until the mechanism of action is further defined and large randomized clinical trials are performed to further validate the safety and effectiveness of this treatment. This use of botulinum toxin in this setting is not FDA-approved.



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2. AUA Practice Guidelines Committee. AUA guideline on management of benign prostatic hyperplasia (2003). Chapter 1: diagnosis and treatment recommendations. J Urol. 2003;170(2, pt 1):530-547.
3. Caine M, Perlberg S, Meretyk S. A placebo-controlled double-blind study of the effect of phenoxybenzamine in benign prostatic obstruction. Br J Urol. 1978;50:551-554.
4. Caine M. The present role of alpha-adrenergic blockers in the treatment of benign prostatic hypertrophy. J Urol. 1986;136:1-4.
5. Lepor H, Lowe FC. Evaluation and nonsurgical management of benign prostatic hyperplasia. In: Walsh PC, Retik AB, Vaughan ED, et al, eds. Campbell’s Urology. 8th ed. Philadelphia: WB Saunders; 2002:1337-1378.
6. Djavan B, Marberger M. A meta-analysis on the efficacy and tolerability of alpha1-adrenoceptor antagonists in patients with lower urinary tract symptoms suggestive of benign prostatic obstruction. Eur Urol. 1999;36:1-13.
7. Lepor H. Long-term efficacy and safety of terazosin in patients with benign prostatic hyperplasia. Terazosin Research Group. Urology. 1995;45:406-413.
8. Lepor H, Kaplan SA, Klimberg I, et al. Doxazosin for benign prostatic hyperplasia: long-term efficacy and safety in hypertensive and normotensive patients. The Multicenter Study Group. J Urol. 1997;157:525-530.
9. van Dijk MM, de la Rosette JJ, Michel MC. Effects of alpha(1)-adrenoceptor antagonists on male sexual function. Drugs. 2006;66:287-301.
10. Major cardiovascular events in hypertensive patients randomized to doxazosin vs chlorthalidone: the antihypertensive and lipid-lowering treatment to prevent heart attack trial (ALLHAT). ALLHAT Collaborative Research Group [published correction appears in JAMA. 2002;288:2976]. JAMA. 2000;283:1967-1975.
11. McConnell JD, Roehrborn CG, Bautista OM, et al. The long-term effect of doxazosin, finasteride, and combination therapy on the clinical progression of benign prostatic hyperplasia. N Engl J Med. 2003;349:2387-2398.
12. Roehrborn CG. Alfuzosin 10 mg once daily prevents overall clinical progression of benign prostatic hyperplasia but not acute urinary retention: results of a 2-year placebo-controlled study. BJU Int. 2006;97:734-741.
13. McConnell JD, Bruskewitz R, Walsh P, et al. The effect of finasteride on the risk of acute urinary retention and the need for surgical treatment among men with benign prostatic hyperplasia. Finasteride Long-Term Efficacy and Safety Study Group. N Engl J Med. 1998;338:557-563.
14. Thompson IM, Goodman PJ, Tangen CM, et al. The influence of finasteride on the development of prostate cancer. N Engl J Med. 2003;349:215-224.
15. Roehrborn CG. The clinical benefits of dutasteride treatment for LUTS and BPH. Rev Urol. 2004;6(suppl 9):S22-S30.
16. Andriole GL, Roehrborn C, Schulman C, et al. Effect of dutasteride on the detection of prostate cancer in men with benign prostatic hyperplasia. Urology. 2004;64:537-541.
17. Boyle P, Gould AL, Roehrborn CG. Prostate volume predicts outcome of treatment of benign prostatic hyperplasia with finasteride: meta-analysis of randomized clinical trials. Urology. 1996;48:398-405.
18. Roehrborn CG, Siami P, Barkin J, et al. The effects of dutasteride, tamsulosin, and combination therapy in men with benign prostatic hyperplasia and prostatic enlargement: 2-year results from the CombAT study. J Urol. 2008;179:616-621.
19. Barkin J, Guimar˜aes M, Jacobi G, et al. Alphablocker therapy can be withdrawn in the majority of men following initial combination therapy with the dual 5alpha-reductase inhibitor dutasteride. Eur Urol. 2003;44:461-466.
20. Kaplan SA, Roehrborn CG, Rovner ES, et al. Tolterodine and tamsulosin for treatment of men with lower urinary tract symptoms and overactive bladder: a randomized controlled trial [published corrections appear in JAMA. 2007;297:1195; JAMA. 2007;298:1864]. JAMA. 2006;296:2319-2328.
21. Blake-James BT, Rashidian A, Ikeda Y, Emberton M. The role of anticholinergics in men with lower urinary tract symptoms suggestive of benign prostatic hyperplasia: a systematic review and meta-analysis. BJU Int. 2007;99:85-96.
22. McVary KT, Roehrborn CG, Kaminetsky JC, et al. Tadalafil relieves lower urinary tract symptoms secondary to benign prostatic hyperplasia. J Urol. 2007;177:1401-1407.
23. Barnes PM, Powell-Griner E, McFann K, Nahin RL. Complementary and alternative medicine use among adults: United States, 2002. Adv Data. 2004;343:1-19.
24. Lowe FC, Fagelman E. Phytotherapy in the treatment of benign prostatic hyperplasia: an update. Urology. 1999;53:671-678.
25. Bent S, Kane C, Shinohara K, et al. Saw palmetto for benign prostatic hyperplasia. N Engl J Med. 2006;354:557-566.
26. Bouza C, López T, Magro A, et al. Systematic review and meta-analysis of Transurethral Needle Ablation in symptomatic Benign Prostatic Hyperplasia. BMC Urol. 2006;6:14.
27. Hoffman RM, MacDonald R, Monga M, Wilt TJ. Transurethral microwave thermotherapy vs transurethral resection for treating benign prostatic hyperplasia: a systematic review. BJU Int. 2004;94:1031-1036.
28. Sandhu JS, Ng C, Vanderbrink BA, et al. Highpower potassium-titanyl-phosphate photoselective laser vaporization of prostate for treatment of benign prostatic hyperplasia in men with large prostates. Urology. 2004;64:1155-1159.
29. Sandhu JS, Ng CK, Gonzalez RR, et al. Photoselective laser vaporization prostatectomy in men receiving anticoagulants. J Endourol. 2005;19:1196-1198.
30. Reich O, Bachmann A, Siebels M, et al. High power (80 W) potassium-titanyl-phosphate laser vaporization of the prostate in 66 high risk patients. J Urol. 2005;173:158-160.
31. Fu WJ, Hong BF, Wang XX, et al. Evaluation of greenlight photoselective vaporization of the prostate for the treatment of high-risk patients with benign prostatic hyperplasia. Asian J Androl. 2006;8:367-371.
32. Barber NJ, Zhu G, Donohue JF, et al. Use of expired breath ethanol measurements in evaluation of irrigant absorption during high-power potassium titanyl phosphate laser vaporization of prostate. Urology. 2006;67:80-83.
33. Bachmann A, Schürch L, Ruszat R, et al. Photoselective vaporization (PVP) versus transurethral resection of the prostate (TURP): a prospective bicentre study of perioperative morbidity and early functional outcome. Eur Urol. 2005;48:965-972.
34. Sarica K, Alkan E, Lüleci H, Tasci AI. Photoselective vaporization of the enlarged prostate with KTP laser: long-term results in 240 patients. J Endourol. 2005;19:1199-1202.
35. Malek RS, Kuntzman RS, Barrett DM. Photoselective potassium-titanyl-phosphate laser vaporization of the benign obstructive prostate: observations on long-term outcomes. J Urol. 2005;174(4, pt 1):1344-1348.
36. Kuntz RM. Current role of lasers in the treatment of benign prostatic hyperplasia (BPH). Eur Urol. 2006;49:961-969.
37. Westenberg A, Gilling P, Kennett K, et al. Holmium laser resection of the prostate versus transurethral resection of the prostate: results of a randomized trial with 4-year minimum long-term followup. J Urol. 2004;172:616-619.
38. Kuntz RM, Ahyai S, Lehrich K. Transurethral holmium laser enucleation of the prostate (HoLEP) compared with TURP: 3 years follow-up results of a randomized clinical trial on 200 patients. Proc SPIE. 2006;6078:10.
39. Oeconomou A, Madersbacher H, Kiss G, et al. Is botulinum neurotoxin type A (BoNT-A) a novel therapy for lower urinary tract symptoms due to benign prostatic enlargement? A review of the literature. Eur Urol. 2008;54:765-775.

Therapeutic Agents in This Article
Alfuzosin (Uroxatral)
Botulinum toxin (Botox)
Chlorthalidone (Clorpres, Thalitone)
Doxazosin (Cardura)
Dutasteride (Avodart)
Finasteride (Proscar)
Phenoxybenzamine (Dibenzyline)
Saw palmetto
Tadalafil (Cialis)
Tamsulosin (Flomax)
Terazosin (Hytrin)
Tolterodine extended-release (Detrol LA)

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