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1.
J Endourol ; 38(5): 521-528, 2024 May.
Article in English | MEDLINE | ID: mdl-38299559

ABSTRACT

Introduction: The most recent American Urological Association (AUA) Guidelines advocated laser enucleation of the prostate (LEP) as a size-independent surgical option for benign prostatic hyperplasia (BPH). Despite its endorsement by AUA and the growing body of evidence supporting its safety and efficacy, the utilization of LEP remains limited in the United States. This study aimed to evaluate the utilization trends and perioperative outcomes of LEP compared with other surgical procedures used for BPH management. Methods: A retrospective cohort analysis was performed using American College of Surgeons National Surgical Quality Improvement Program data from 2011 to 2020. Patients undergoing prostatectomy for BPH were identified using specific current procedural terminology (CPT) codes. Baseline demographic data, preoperative risk factors, and postoperative outcomes were collected. Multivariable logistic regression was employed to assess predictors of holmium laser enucleation of the prostate (HoLEP) utilization and postoperative complications. Results: Out of 8,415,549 patients, 95,144 underwent prostatectomy for BPH. Procedures included HoLEP 5305 cases, transurethral resection of the prostate (TURP) 57,803 cases, repeated TURP (re-TURP) 5549 cases, photoselective vaporization of the prostate (PVP) 23,739 cases, and simple prostatectomy 2748 cases. HoLEP utilization showed a gradual increase, from 4.8% in 2015 to 7.6% in 2020. Multivariable regression revealed that HoLEP selection significantly increased from 2016 to 2020 (odds ratio [OR]: 1.251, p < 0.001), and there was less likelihood of HoLEP selection for African American patients (OR: 0.752, p < 0.001). HoLEP had significantly lower complication rates, including urinary tract infections, blood transfusions, 30-day readmission, and reoperation. Conclusion: Despite underutilization, the adoption of HoLEP has slightly increased since 2015, rising from 4.8% in 2015 to 7.6% in 2020. The underutilization could be attributed to a lack of availability and the steep learning curve.


Subject(s)
Lasers, Solid-State , Prostatectomy , Prostatic Hyperplasia , Quality Improvement , Humans , Male , Lasers, Solid-State/therapeutic use , Aged , United States , Retrospective Studies , Prostatic Hyperplasia/surgery , Middle Aged , Prostatectomy/methods , Databases, Factual , Postoperative Complications/epidemiology , Prostate/surgery , Prostate/pathology , Laser Therapy/methods
2.
Article in English | MEDLINE | ID: mdl-36641534

ABSTRACT

BACKGROUND: High-risk prostate cancer includes heterogenous populations with variable outcomes. This study aimed to compare the prognostic ability of individual high-risk factors, as defined by National Comprehensive Cancer Network (NCCN) risk stratification, in prostate cancer patients undergoing radical prostatectomy. METHODS: We queried the National Cancer Database from 2004 to 2018 for patients with non-metastatic high-risk prostate cancer who underwent radical prostatectomy and stratified them as Group H1: Prostate specific antigen (PSA) > 20 ng/ml alone, Group H2: cT3a stage alone and Group H3: Gleason Grade (GG) group 4/5 as per NCCN guidelines. The histopathological characteristics and rate of adjuvant therapy were compared between different groups. Inverse probability weighting (IPW)-adjusted Kaplan-Meier curves were utilized to compare overall survival (OS) in group H1 and H2 with H3. RESULTS: Overall, 61,491 high-risk prostate cancer patients were identified, and they were classified into Group H1 (n = 14,139), Group H2 (n = 2855) and Group H3 (n = 44,497). Compared to group H1 or H2, pathological GG group > 3 (p < 0.001), pathological stage pT3b or higher (p < 0.001), lymph nodal positive disease (pN1) (p < 0.001) and rate of adjuvant therapy (p < 0.001) were significantly in Group H3. IPW-adjusted Kaplan-Meier curves showed significantly better 5-year OS in group H1 compared to group H3 [95.1% vs 93.3%, p < 0.001] and group H2 compared to group H3 [94.4% vs 92.9%, p < 0.001]. CONCLUSION: PSA > 20 ng/ml or cT3a stage in isolation have better oncologic and survival outcomes compared to GG > 3 disease and sub-stratification of 'High-risk' category might lead to better patient prognostication.

3.
Mol Med Rep ; 20(3): 2667-2674, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31524262

ABSTRACT

The newly identified Src homology and collagen (Shc) family member ShcD was observed to be upregulated in 50% of vertical growth phase and metastatic melanomas. The aim of the present study was to investigate the mechanism by which ShcD mediates cell motility. 293 cell lines were altered to stably express GFP (GF) or GFP­ShcD (G5). Treatment of the cells with transforming growth factor (TGF)ß2 promoted extracellular signal­regulated kinase (ERK) phosphorylation and, to a lesser extent, Smad2 phosphorylation in GFP­ShcD­expressing cells but not in GFP­overexpressing cells. GFP­ShcD­expressing cells exhibited upregulated expression of certain epithelial­mesenchymal transition­related genes, such as snail family transcriptional repressor 1 and SLUG, than GFP­expressing cells. Higher levels of ERK were found in the nuclear fraction of GFP­ShcD­expressing cells than that of GFP­expressing cells. Overall, GFP­ShcD­expressing cells demonstrated enhanced migration compared with GFP­expressing cells. A slight increase in cell migration was observed in both cell lines (GF and G5) when the cells were allowed to migrate towards conditioned medium derived from TGFß2­treated GFP­ShcD expressing cells. Collectively, ShcD upregulation was proposed to induce cell migration by affecting the expression of certain epithelial­mesenchymal transition­related genes. Thus, our findings may improve understanding of the role of ShcD in cell migration.


Subject(s)
Gene Expression , Shc Signaling Adaptor Proteins/genetics , Transforming Growth Factor beta/metabolism , Cell Line , Cell Movement/genetics , Extracellular Signal-Regulated MAP Kinases/metabolism , Genes, Reporter , HEK293 Cells , Humans , Phosphorylation , Receptor, Transforming Growth Factor-beta Type I/genetics , Receptor, Transforming Growth Factor-beta Type I/metabolism , Shc Signaling Adaptor Proteins/metabolism
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