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Randomized Controlled Trial
. 2012:2012:463574.
doi: 10.1100/2012/463574. Epub 2012 Sep 10.

Botulinum neurotoxin type A for the treatment of benign prostatic hyperplasia: randomized study comparing two doses

Affiliations
Randomized Controlled Trial

Botulinum neurotoxin type A for the treatment of benign prostatic hyperplasia: randomized study comparing two doses

René Arnouk et al. ScientificWorldJournal. 2012.

Abstract

Purpose: To assess the efficacy and safety of intraprostatic injection of two botulinum neurotoxin type A (BoNT-A) doses for the treatment of benign prostatic hyperplasia (BPH).

Materials and methods: Men with symptomatic BPH who failed medical treatment were randomized to receive 100 U or 200 U of BoNT-A into the prostate. The International Prostatic Symptom Score (IPSS), maximum flow rate (Q(max)), post-void residual volume (PVR), PSA levels and prostate volume before injection and after 3 and 6 months were evaluated. Adverse events were compared between the groups.

Results: Thirty four patients were evaluated, including 17 in the BoNT-A 100 U group and 17 in the BoNT-A 200 U group. Baseline characteristics were similar in both groups. Both doses produced significant improvements in IPSS, Q(max) and PVR after 3 and 6 months and both doses promoted comparable effects. Prostate volume was affected by 200 U BoNT-A injection only after 6 months of treatment. PSA levels were significantly affected in the 100 U group only after 6 months of treatment. In the 200 U group, PSA levels were significantly decreased after 3 and 6 months. The complication rate was similar in both groups.

Conclusions: Efficacy and safety of both BoNT-A doses are similar for BPH treatment in the short term followup.

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Figures

Figure 1
Figure 1
Mean IPSS of 34 patients treated with 100 and 200 U of intraprostatic BoNT-A.
Figure 2
Figure 2
Mean Qmax⁡ of 34 patients treated with 100 and 200 U of intraprostatic BoNT-A.
Figure 3
Figure 3
Mean PVR of 34 patients treated with 100 and 200 U of intraprostatic BoNT-A.

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