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We appreciate the commentary by Manfredi et al. on our study investigating the impact of phosphodiesterase type 5 inhibitors (PDE5is) on Peyronie’s disease (PD) in the active phase [1]. The
attention devoted to non-surgical interventions in PD in recent years highlights a growing recognition of the need for effective non-invasive treatments for this condition. This increased
focus may reflect a broader shift in medical practice towards holistic patient care, emphasizing options beyond surgical intervention. Despite the paucity of clinical studies, PDE5is hold
promise as a viable, safe, and practical approach to managing the condition, potentially offering relief and influencing its progression [2, 3]. With their generally well-tolerated nature
and favorable safety profile [4], PDE5is emerge as an appealing choice for PD management.
In our retrospective cohort study, 133 patients with PD in the active phase were included. Group 1 (n = 101) received continuous treatment with PDE5is, while Group 2 (n = 32) received no
treatment. The curvature progression was recorded over a mean follow-up of approximately one year. Between the first and last observations, Group 1 exhibited a mean penile curvature change
of + 0.87° (95% CI: −1.8, 3.5), whereas Group 2 experienced a larger increase of + 5.72° (95% CI: 1.4, 10). Although there was a numerical difference in curvature progression, it did not
reach statistical significance (p = 0.07), and the variance was small compared to what would be considered clinically meaningful [5]. Meanwhile, Group 1 exhibited a shorter mean duration of
pain of 9.1 months (SD 4.7), compared to Group 2 reporting a mean pain duration of 12.2 months (SD 6.5) (p = 0.04).
ED: Manuscript writing and editing, CFSJ: Manuscript reviewing and editing, MF: Manuscript reviewing, editing and supervision.
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