Best Medications for Benign Prostatic Hyperplasia
For men with moderate-to-severe BPH symptoms and an enlarged prostate (>30cc), combination therapy with tamsulosin 0.4 mg and a 5-alpha-reductase inhibitor (dutasteride or finasteride) is the most effective treatment to improve symptoms and prevent disease progression. 1, 2
Treatment Selection Algorithm
Step 1: Assess Prostate Size and Symptom Severity
- Confirm prostatic enlargement using one of the following criteria: 2
- Prostate volume >30cc on imaging, OR
- PSA >1.5 ng/mL, OR
- Palpable prostate enlargement on digital rectal examination
- Assess symptom severity using validated tools (AUA Symptom Score >8 indicates moderate-to-severe symptoms) 3
Step 2: Choose Therapy Based on Prostate Size
For enlarged prostates (>30cc) with moderate-to-severe symptoms:
- Initiate combination therapy with tamsulosin 0.4 mg daily plus either dutasteride 0.5 mg or finasteride 5 mg daily 1, 2
- Combination therapy reduces overall BPH clinical progression by 67% compared to 39% for alpha-blockers alone and 34% for 5-alpha-reductase inhibitors alone 1
- The best-tested combination is doxazosin and finasteride, though the combination of any effective alpha-blocker and 5-alpha-reductase inhibitor likely produces comparable benefit 3
For smaller prostates (<30cc) with moderate-to-severe symptoms:
- Use tamsulosin monotherapy 0.4 mg once daily 4, 5
- Alpha-blockers do not reduce prostate size and should not be used for this purpose 4
- 5-alpha-reductase inhibitors are ineffective in patients without prostatic enlargement 1
Medication-Specific Considerations
Tamsulosin (Alpha-Blocker)
- Standard dose: 0.4 mg once daily, no titration required 4
- Onset of action: Rapid symptom relief (within days to weeks) 2
- Efficacy: Improves symptoms by 12% and increases peak urine flow by 1.1 mL/sec compared to placebo 6
- Does not reduce prostate size 4
Finasteride (5-Alpha-Reductase Inhibitor)
- FDA-approved indications: 7
- Monotherapy for symptomatic BPH to improve symptoms, reduce acute urinary retention risk, and reduce need for surgery
- Combination with alpha-blocker (specifically doxazosin) to reduce symptomatic progression
- Onset of action: Slower (3-6 months for noticeable improvement) 1
- Reduces prostate volume and PSA levels by approximately 50% after 1 year 1, 2
Dutasteride (Dual 5-Alpha-Reductase Inhibitor)
- More potent than finasteride: Reduces serum DHT by ~95% vs ~70% with finasteride 1
- Reduces prostate volume by 15-25% after 6 months 1
- Reduces clinical progression: 21% vs 36% with placebo (includes AUR, UTI, or need for surgery) 1
- Sustained long-term benefit maintained for 6-10 years 1
Critical Timing Considerations
Combination therapy provides additive benefits with different time courses: 2
- Tamsulosin provides relatively rapid symptom relief (weeks)
- 5-alpha-reductase inhibitors provide slower onset but long-term benefits in reducing prostate size and preventing progression (months)
This dual mechanism explains why combination therapy is superior to either monotherapy alone in men with enlarged prostates 8, 9
Important Safety Warnings and Pitfalls
Before Starting Tamsulosin:
- Inform ophthalmologists if patient is planning cataract or glaucoma surgery due to risk of intraoperative floppy iris syndrome 1, 4, 5
- Higher risk of ejaculatory dysfunction compared to other alpha-blockers 4
- Risk of orthostatic hypotension, especially after first dose 5
Before Starting 5-Alpha-Reductase Inhibitors:
- Counsel patients that PSA levels will decrease by ~50% after 1 year of therapy 1, 2
- Double the measured PSA value after 1 year of therapy when screening for prostate cancer 1, 2
- Sexual side effects including decreased libido, erectile dysfunction, and ejaculatory disorders occur more frequently than with placebo 7
- Not approved for prostate cancer prevention 7
Common Pitfall to Avoid:
Do not use combination therapy in patients without prostatic enlargement - this exposes patients to unnecessary side effects without benefit, as 5-alpha-reductase inhibitors are ineffective in smaller prostates 1
Adverse Effects Profile
Combination Therapy (from MTOPS trial):
The most common adverse effects with combination therapy include: 7
- Abnormal ejaculation: 14.1% (vs 2.3% placebo)
- Impotence: 22.6% (vs 12.2% placebo)
- Decreased libido: 11.6% (vs 5.7% placebo)
- Dizziness: 23.2% (vs 8.1% placebo)
- Postural hypotension: 17.8% (vs 8.0% placebo)
The incidence of abnormal ejaculation with combination therapy was comparable to the sum of incidences from both monotherapies 7