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Can we use baseline characteristics to assess which men with moderately symptomatic benign prostatic hyperplasia at risk of progression will benefit from treatment? A post hoc analysis of data from the 2-year CONDUCT study. | LitMetric

AI Article Synopsis

  • The study aimed to explore how lifestyle changes can help men with moderate benign prostatic hyperplasia (BPH) who are at risk of worsening symptoms.
  • Patients were divided into two groups: one received a combination medication (dutasteride and tamsulosin) while the other was monitored without immediate treatment, following their symptoms over 24 months.
  • Findings suggested that lifestyle advice and no treatment showed similar symptom improvements, indicating that baseline quality of life measures (BPH Impact Index) could be more important than just symptom severity when considering medical treatment options.

Article Abstract

Purpose: To investigate (in a post hoc analysis of the 2-year CONDUCT study) the characteristics and clinical outcomes of men with moderately symptomatic benign prostatic hyperplasia (BPH) at risk of progression who benefitted from lifestyle changes alone.

Methods: Patients were given lifestyle advice and randomized to a fixed-dose combination (FDC) of dutasteride and tamsulosin or watchful waiting (WW) and followed for 24 months. Patients in the WW group were escalated to tamsulosin if any follow-up International Prostate Symptom Score (IPSS) was equal or greater than the baseline value. Improvements in symptoms (change in IPSS) and quality of life [measured by BPH Impact Index (BII) and question 8 of the IPSS (IPSS-Q8)] were analysed in the FDC group, men who initiated tamsulosin (WW-TAM) and men who received no medical intervention (WW-no treatment) and the impact of baseline variables on IPSS determined.

Results: The adjusted mean decrease in IPSS, BII and IPSS-Q8 at each post-baseline visit over 24 months appeared greater in the FDC (n = 369) and WW-no treatment groups (n = 144) than in the WW-TAM group (n = 229). IPSS improvements appeared similar in the FDC group and WW-no treatment subgroup, except in patients with the greatest degree of bother at baseline (BII 7-13).

Conclusion: BII at baseline may be a more relevant indicator than symptom severity as to whether a patient with moderate symptoms should receive medical therapy or not.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332489PMC
http://dx.doi.org/10.1007/s00345-016-1884-5DOI Listing

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