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1.
World J Urol ; 42(1): 113, 2024 Mar 02.
Article in English | MEDLINE | ID: mdl-38431689

ABSTRACT

PURPOSE: To compare the efficacy and safety of mirabegron and vibegron in female OAB patients. METHODS: We conducted a multicenter, prospective, randomized crossover study of female patients with OAB. The patients were assigned to Group MV (mirabegron for 8 weeks, followed by vibegron for 8 weeks) or group VM (vibegron for 8 weeks, followed by mirabegron for 8 weeks). The primary endpoint was the change in OABSS from baseline, and the secondary endpoint was the change in FVC parameters. After completion of the study, each patient was asked which drug was preferable. RESULTS: A total of 83 patients were enrolled (40 and 43 in groups MV and VM, respectively). At 8th and 16th week, 33 and 29 in Group MV and 34 and 27 in Group VM continued to receive the treatment. The change in PVR was not significantly different between treatment with mirabegron and vibegron. The changes in OABSS, nighttime frequency, mean, and maximum voided volume were similar between mirabegron and vibegron. The mean change in the daytime frequency was greater in the vibegron than in the mirabegron. Of the 56 patients, 15 (27%) and 30 (53%) preferred mirabegron and vibegron, respectively. The remaining 11 patients (20%) showed no preference. The change in the urgency incontinence score during vibegron was better in patients who preferred vibegron to mirabegron. CONCLUSION: The efficacies of mirabegron and vibegron in female patients was similar. The patients' preference for vibegron could depend on the efficacy of vibegron for urgency incontinence.


Subject(s)
Pyrimidinones , Pyrrolidines , Thiazoles , Urinary Bladder, Overactive , Urinary Incontinence , Urological Agents , Humans , Female , Urinary Bladder, Overactive/drug therapy , Urinary Bladder, Overactive/complications , Cross-Over Studies , Prospective Studies , Acetanilides/therapeutic use , Treatment Outcome , Double-Blind Method , Urological Agents/therapeutic use , Adrenergic beta-3 Receptor Agonists/therapeutic use
2.
Diagn Pathol ; 7: 173, 2012 Dec 07.
Article in English | MEDLINE | ID: mdl-23217062

ABSTRACT

Prostatic stromal sarcoma is a fairly rare tumor that constitutes approximately 0.1-0.2% of all prostatic cancers. Detailed characteristics of the tumor are still unclear due to its rarity.We describe a case of prostatic stromal sarcoma in a 63 year-old man who suffered from urinary obstructive symptoms. Palliative transuterine resection was performed and the preliminary histopathological diagnosis was neuroendocrine carcinoma. After chemotherapy, total pelvic exenteration was performed. Histopathologically, the tumor was composed of monotonously proliferating small to medium-sized round cells, which existed in compact islands with loose or dense fibrovascular networks. Immunohistochemically, the tumor cells were widely positive for vimentin, CD56, CD99 and focally positive for synaptophysin, CD10, progesterone receptor, desmin and CD34, but negative for EMA, cytokeratin, estrogen receptor, S-100 and myoglobin. Most of the previously reported tumors exhibited positive stainability for CD10 and progesterone receptor. In addition to these markers, expressions of CD56, CD99 and synaptophysin were characteristically detected in our case. To the best of our knowledge, we present the first case of prostatic stromal sarcoma with characteristic immunohistochemical staining properties. Although the biological characteristics of this rare tumor have not yet been elucidated, these findings suggest prostatic stromal sarcoma can potentially show neuroectodermal differentiation. VIRTUAL SLIDE: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/7291874028051262.


Subject(s)
Cell Differentiation , Neoplasms, Complex and Mixed/pathology , Neuroectodermal Tumors/pathology , Prostatic Neoplasms/pathology , Sarcoma/pathology , Stromal Cells/pathology , Biomarkers, Tumor/analysis , Cell Proliferation , Humans , Immunohistochemistry , Magnetic Resonance Imaging , Male , Middle Aged , Neoplasms, Complex and Mixed/chemistry , Neoplasms, Complex and Mixed/therapy , Neuroectodermal Tumors/chemistry , Neuroectodermal Tumors/therapy , Prostatic Neoplasms/chemistry , Prostatic Neoplasms/therapy , Sarcoma/chemistry , Sarcoma/surgery , Stromal Cells/chemistry , Tomography, X-Ray Computed , Treatment Outcome
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