Medications for Benign Prostatic Hyperplasia
For a typical older male with BPH, start with an alpha-blocker (terazosin, doxazosin, or tamsulosin) for rapid symptom relief, and add a 5-alpha reductase inhibitor (finasteride 5 mg or dutasteride 0.5 mg daily) if the prostate is enlarged (>30-40 mL) to prevent disease progression and reduce long-term risks of acute urinary retention and surgery. 1, 2
Initial Treatment Selection
Alpha-Blockers as First-Line Therapy
- Alpha-blockers provide rapid symptom relief within days to weeks and are the initial therapy of choice for most patients with moderate to severe lower urinary tract symptoms (LUTS). 1, 3
- Effective options include terazosin (1-20 mg daily), doxazosin (1-16 mg daily), or tamsulosin (0.4 mg daily). 1
- Alpha-blockers work by relaxing smooth muscle in the bladder neck, prostatic adenoma, and prostatic capsule, decreasing resistance to urine flow. 4
- Compared to placebo, alpha-blockers produce 15-20% improvements in maximum urinary flow rate and symptom score reductions. 5
Important caveat: Tamsulosin requires no dose titration and lacks significant blood pressure effects, making it preferable in normotensive patients, while terazosin and doxazosin are better choices for hypertensive patients with BPH since they provide dual benefit. 5, 1
When to Add 5-Alpha Reductase Inhibitors
- Add a 5-ARI (finasteride 5 mg daily or dutasteride 0.5 mg daily) if the prostate volume is >30-40 mL, as these medications are ineffective in men without prostatic enlargement. 1, 3
- 5-ARIs block conversion of testosterone to dihydrotestosterone (DHT), reducing prostate volume by approximately 18-25% over 6-12 months. 6, 7
- Finasteride reduces the risk of acute urinary retention and need for BPH-related surgery, with absolute benefit increasing with higher prostate volume or serum PSA. 1
- Dutasteride achieves greater reductions in prostate volume (-26.3% vs -18.1%) and PSA levels (-43.7% vs -32.5%) compared to finasteride. 8
Critical timing consideration: Patients must wait 3-6 months to see full effects of 5-ARIs due to their slower onset of action, unlike the rapid relief from alpha-blockers. 3, 5
Combination Therapy
- Combination therapy with an alpha-blocker plus a 5-ARI is indicated for patients with enlarged prostates (>30 mL) who need both rapid symptom relief and long-term disease modification. 2, 3
- The combination addresses both the dynamic component (smooth muscle tone via alpha-blocker) and static component (prostate size via 5-ARI) of bladder outlet obstruction. 3, 6
- Finasteride combined with doxazosin reduces the risk of symptomatic BPH progression (confirmed ≥4 point increase in AUA symptom score). 2
- In the MTOPS trial, combination therapy showed superior outcomes compared to monotherapy, particularly in patients with larger prostates. 1, 2
Common pitfall: Combination therapy increases the incidence of certain adverse effects—asthenia, postural hypotension, peripheral edema, dizziness, decreased libido, and abnormal ejaculation occur more frequently than with either drug alone. 2
Monitoring and Follow-Up
- Evaluate patients 4-12 weeks after initiating alpha-blocker therapy to assess response and side effects. 3
- For 5-ARIs, wait 3-6 months before assessing efficacy, as maximum prostate shrinkage requires at least 12 months. 3, 5
- Follow-up should include International Prostate Symptom Score (IPSS), quality of life assessment, evaluation of medication side effects, and when available, uroflowmetry and post-void residual measurement. 3
- 5-ARIs reduce PSA by approximately 50%, which must be considered when monitoring for prostate cancer—multiply PSA values by 2 in patients on 5-ARIs. 3, 7
Side Effect Profile
Alpha-Blocker Side Effects
- Orthostatic hypotension and dizziness are common, especially in older adults. 1
- Tamsulosin has lower rates of cardiovascular side effects but higher probability of ejaculatory dysfunction compared to other alpha-blockers. 1
5-ARI Side Effects
- Sexual side effects are the most common adverse events: decreased libido (6.4% vs 3.4% placebo), erectile dysfunction (8.1% vs 3.7% placebo), and ejaculatory dysfunction (3.7% vs 0.8% placebo) in the first year. 2
- These side effects are typically reversible and decrease after the first year of therapy. 1, 3
- Sexual dysfunction may persist beyond drug discontinuation in some patients. 2
- Breast tenderness (0.4%) and breast enlargement (0.5%) can occur. 2
Critical safety concern: The PCPT trial showed higher incidence of Gleason score 8-10 prostate cancer in men treated with finasteride (1.8%) versus placebo (1.1%), though finasteride is not approved for prostate cancer prevention. 2
When Medical Therapy Fails
- Refer for surgical intervention (TURP or alternative minimally invasive procedures) if symptoms continue to worsen or fail to improve after 6 months of combination therapy. 6
- Absolute indications for surgery include renal insufficiency secondary to BPH, refractory urinary retention, recurrent urinary tract infections, or recurrent bladder stones. 6