Las biopsias de próstata dirigidas ¿están listas para reemplazar las biopsias de próstata sistemáticas? / Are targeted prostate biopsies ready to replace systematic prostate biopsies?

Objetivos: Evaluar la eficacia y la eficiencia de la biopsia prostática sistemática (BPS) y la biopsia de próstata por fusión cognitiva (BPFC) para diagnosticar el cáncer de próstata (CaP) y el CaP significativo (CaPs) y analizar si la BPFC podría reemplazar con seguridad a la BPS. Material y métodos: Una cohorte de 314 hombres consecutivos que tenían PI-RADS ≥2 en una biopsia previa 3T resonancia magnética multiparamétrica se sometieron prospectivamente a BPFC ecográfica transrectal (dos núcleos por área sospechosa hasta un máximo de tres áreas) y una BPS de 12 núcleos periféricos. Se consideró CaPs cuando el grado de la OMS fue superior a 2 (Gleason 4 + 3 o superior). Resultados: Se diagnosticó CaP en 133 pacientes (42,4%), de los que 83 (62,4%) fueron CaPs. La BPS detectó CaP en 114 hombres (85,7%) y BPFC en 103 (77,4%), p < 0,001. La BPS detectó CaPs en 64 hombres (77,1%) y BPFC en 71 (85,5%), p < 0,001. En 52 de los 81 hombres (64,2%) se detectó CaPs en BPS y BPFC. En 19 hombres solo se detectó CaPs en BPFC (23,5%), mientras que en 10 solo se detectó en BPS (12,3%). Se necesitaron 33,1 núcleos para diagnosticar un CaP en BPS y 8,5 en BPFC, p < 0,001. 58,9 núcleos fueron necesarios para diagnosticar un CaPs en BPS y 12,4 en BPFC, p < 0,001. Conclusiones: Las BPFC son más efectivas y también más eficientes que las BPS para detectar CaPs. Sin embargo, las BPFC aún no pueden reemplazar las BPS de manera segura porque no pueden detectar hasta el 15% de los CaPs

Objectives: To evaluate the efficacy and efficiency of systematic prostatic biopsy (SPB) and cognitive fusion PB (CFPB) to diagnose prostate cancer (PCa) and significant PCa (SPCa), and to analyse if CFPB could safely replace SPB. Material and methods: A cohort of 314 consecutive men having PI-RADS ≥ 2 in a pre-biopsy 3T mp-MRI were prospectively subjected to trans-rectal ultrasound CFPB (two cores per suspicious area until a maximum of three areas) and a 12 peripheral core SPB. SPCa was considered when the WHO grade was higher than 2 (Gleason 4+3 or higher). Results: PCa was diagnosed in 133 patients (42.4%), being 83 (62.4%) SPCa. SPB detected PCa in 114 men (85.7%) while CFPB in 103 (77.4%), P < .001. SPB detected SPCa in 64 men (77.1%) while CFPB in 71 (85.5%), P < .001. In 52 of the 81 men (64.2%) SPCa was detected in SPB and CFPB. In 19 men SPCa was only detected in CFPB (23.5%) while in 10, it was only detected in SPB (12.3%). 33.1 cores were needed to diagnose one PCa in SPB while 8.5 in CFPB, P < .001. 58.9 cores were needed to diagnose one SPCa in SPB, while 12.4 in CFPB, P < .001. Conclusions: CFPB are more effective and also more efficient than SPBs in detecting SPCa. However, CFPBs still can’t safely replace SPBs because they are not able to detect up to 15% of SPCa

Are targeted prostate biopsies ready to replace systematic prostate biopsies? / Las biopsias de próstata dirigidas ¿están listas para reemplazar las biopsias de próstata sistemáticas?

OBJECTIVES: To evaluate the efficacy and efficiency of systematic prostatic biopsy (SPB) and cognitive fusion PB (CFPB) to diagnose prostate cancer (PCa) and significant PCa (SPCa), and to analyse if CFPB could safely replace SPB. MATERIAL AND METHODS: A cohort of 314 consecutive men having PI-RADS ≥2 in a pre-biopsy 3T mp-MRI were prospectively subjected to trans-rectal ultrasound CFPB (two cores per suspicious area until a maximum of three areas) and a 12 peripheral core SPB. SPCa was considered when the WHO grade was higher than 2 (Gleason 4+3 or higher). RESULTS: PCa was diagnosed in 133 patients (42.4%), being 83 (62.4%) SPCa. SPB detected PCa in 114 men (85.7%) while CFPB in 103 (77.4%), P<.001. SPB detected SPCa in 64 men (77.1%) while CFPB in 71 (85.5%), P<.001. In 52 of the 81 men (64.2%) SPCa was detected in SPB and CFPB. In 19 men SPCa was only detected in CFPB (23.5%) while in 10, it was only detected in SPB (12.3%). 33.1 cores were needed to diagnose one PCa in SPB while 8.5 in CFPB, P<.001. 58.9 cores were needed to diagnose one SPCa in SPB, while 12.4 in CFPB, P<.001. CONCLUSIONS: CFPB are more effective and also more efficient than SPBs in detecting SPCa. However, CFPBs still can't safely replace SPBs because they are not able to detect up to 15% of SPCa.

Análisis del escenario microscópico de una biopsia prostática negativa como predictor del riesgo de cáncer de próstata. Una revisión sistemática / In Search for risk predictors at the microscopic scenario of a negative biopsy. A systematic review

Introducción: Las biopsias prostáticas (BP) de repetición, ante la persistencia de la sospecha de cáncer de próstata (CP), son frecuentes y su rendimiento bajo. En el contexto de una BP negativa existe un escenario microscópico (EM), que definimos como el conjunto de lesiones no neoplásicas identificable. La existencia de algunas de estas lesiones incrementa el riesgo de detección de CP en BP sucesivas, mientras que otras parecen tener un efecto protector. El objetivo de esta revisión sistemática es identificar el conjunto de lesiones que puede formar parte del EM de una BP negativa y analizar la evidencia actual de su asociación con el riesgo de detección de CP en BP sucesivas. Adquisición de la evidencia: Dos revisores independientes realizaron una búsqueda bibliográfica en Medline, Embase y Central Cochrane, con los términos de búsqueda: small acinar proliferation or ASAP or prostatic intraepithelial neoplasia or HGPIN or adjacent small atypical glands or pinatyp or atrophy or proliferative inflammatory atrophy or pia or prostatic inflammation or prostatitis and prostate cancer. Se identificaron 1.015 referencias y siguiendo los principios de la declaración PRISMA y de selección PICO, se identificaron 57 artículos originales válidos para esta revisión. Síntesis de la evidencia: La proliferación acinar atípica de célula pequeña se asocia a una tasa de detección de CP en BP sucesivas que oscila entre el 32 y 48%. La neoplasia intraepitelial prostática de alto grado (HGPIN) se asocia a CP entre el 13 y 42%, siendo su multifocalidad la que define el incremento en el riesgo de detección. La atrofia prostática, la atrofia proliferativa inflamatoria y la infamación prostática parecen tener un efecto protector sobre la detección de CP en BP sucesivas. Por otra parte, el riesgo de detección de CP en varones con HGPIN multifocal se reduce significativamente si coexiste atrofia proliferativa inflamatoria. Conclusiones: El EM de una BP negativa puede estar compuesto por las lesiones de proliferación acinar atípica de célula pequeña, HGPIN, atrofia prostática, atrofia proliferativa inflamatoria e infamación prostática ya que todas parecen estar asociadas al riesgo de detección de CP en BP sucesivas. Esta revisión nos permite generar la hipótesis de que el EM de una BP negativa puede ser de utilidad en la decisión indicar BP de repetición

Introduction: In cases of persistent suspicion of prostate cancer (PC), repeat prostate biopsies (PB) are frequently performed in spite of their low yield. In the context of a negative PB, there is a microscopic scenario (MS), which we define as the group of recognizable non-neoplastic lesions. While some of these lesions seem to have a protective effect, the existence of others increases the risk of PC detection in posterior PB. The objective of this systematic review is to identify the lesions that may belong to the MS of a negative PB and analyse the current evidence of their association with the risk of detecting PC in subsequent PBs. Evidence acquisition: Two independent reviewers conducted a literature search on Medline, Embase and Central Cochrane with the following search terms: small acinar proliferation, ASAP, prostatic intraepithelial neoplasia, HGPIN, adjacent small atypical glands, pinatyp, atrophy, proliferative inflammatory atrophy, pia, prostatic inflammation, prostatitis and prostate cancer. 1,015 references were first identified, and 57 original articles were included in the study, following the PRISMA declaration and the PICO selection principles. Evidence synthesis: Atypical small acinar proliferation is associated with PC detection in repeat PB with rates ranging between 32 and 48%. High-grade prostatic intraepithelial neoplasia (HGPIN) is related to PC in 13 to 42% of cases. Studies show that HGPIN, when multifocal, is a significant independent risk factor for PC. Prostatic atrophy, inflammatory proliferative atrophy and prostatic inflammation seem to act as protective factors on the detection of PC in repeat PB. On the other hand, the risk of PC detection reduces significantly in male patients with multifocal HGPIN and coexistent PIA. Conclusions: The MS of a negative PB may include atypical small acinar proliferation, HGPIN, prostatic atrophy, inflammatory proliferative atrophy and prostatic inflammation lesions, since they all seem to be associated with the risk of PC detection in repeat PB. This review has led us to create the hypothesis that the MS of a negative PB might be a valuable and useful tool when considering repeat PB

In Search for risk predictors at the microscopic scenario of a negative biopsy. A systematic review. / Análisis del escenario microscópico de una biopsia prostática negativa como predictor del riesgo de cáncer de próstata. Una revisión sistemática.

INTRODUCTION: In cases of persistent suspicion of prostate cancer (PC), repeat prostate biopsies (PB) are frequently performed in spite of their low yield. In the context of a negative PB, there is a microscopic scenario (MS), which we define as the group of recognizable non-neoplastic lesions. While some of these lesions seem to have a protective effect, the existence of others increases the risk of PC detection in posterior PB. The objective of this systematic review is to identify the lesions that may belong to the MS of a negative PB and analyse the current evidence of their association with the risk of detecting PC in subsequent PBs. EVIDENCE ACQUISITION: Two independent reviewers conducted a literature search on Medline, Embase and Central Cochrane with the following search terms: small acinar proliferation, ASAP, prostatic intraepithelial neoplasia, HGPIN, adjacent small atypical glands, pinatyp, atrophy, proliferative inflammatory atrophy, pia, prostatic inflammation, prostatitis and prostate cancer. 1,015 references were first identified, and 57 original articles were included in the study, following the PRISMA declaration and the PICO selection principles. EVIDENCE SYNTHESIS: Atypical small acinar proliferation is associated with PC detection in repeat PB with rates ranging between 32 and 48%. High-grade prostatic intraepithelial neoplasia (HGPIN) is related to PC in 13 to 42% of cases. Studies show that HGPIN, when multifocal, is a significant independent risk factor for PC. Prostatic atrophy, inflammatory proliferative atrophy and prostatic inflammation seem to act as protective factors on the detection of PC in repeat PB. On the other hand, the risk of PC detection reduces significantly in male patients with multifocal HGPIN and coexistent PIA. CONCLUSIONS: The MS of a negative PB may include atypical small acinar proliferation, HGPIN, prostatic atrophy, inflammatory proliferative atrophy and prostatic inflammation lesions, since they all seem to be associated with the risk of PC detection in repeat PB. This review has led us to create the hypothesis that the MS of a negative PB might be a valuable and useful tool when considering repeat PB.

Valor de la proteína STAT3 como factor pronóstico en el carcinoma renal de célula clara. Revisión sistemática / The role of STAT3 protein as a prognostic factor in the clear cell renal carcinoma. Systematic review

Contexto y objetivo: En los últimos años se han producido avances significativos en el conocimiento de la carcinogénesis renal. Hoy en día los tumores renales se clasifican en función de su perfil genético, y además se han desarrollado tratamientos específicos basados en la identificación de dianas terapéuticas. Sin embargo, todavía no se han identificado marcadores pronósticos. El objetivo de esta revisión es analizar la literatura que ha evaluado la expresión de la proteína STAT3 como marcador molecular en el carcinoma renal de célula clara (ccRCC). Adquisición de evidencia: En enero de 2018 se realizó una búsqueda sistemática de la literatura en Pubmed, Cochrane Library y Sciencedirect de las publicaciones realizadas desde 1990. Los términos de búsqueda fueron renal cell carcinoma and STAT3 or STAT-3 and prognostic factor. Se siguieron los principios de la declaración PRISMA y la estrategia de selección PICO, seleccionándose los artículos originales con series de pacientes diagnosticados de ccRCC localizado o metastásico, donde se analiza la actividad de STAT3 como marcador pronóstico. Se identificaron 132 publicaciones de las que finalmente se han revisado 10 por cumplir los criterios de inclusión. Síntesis de evidencia: La activación (fosforilación) de STAT3 (pSTAT3) en el residuo Ser727 es importante en el desarrollo y progresión de ccRCC. La expresión de pSTAT3 parece ser un marcador pronóstico y predictor de resistencia a algunos tratamientos en pacientes con enfermedad diseminada. Existe poca evidencia de su utilidad como un marcador pronóstico en pacientes con enfermedad localizada. Conclusiones: La expresión de pSTAT3(Ser727) en el núcleo de las células del ccRCC puede ser un marcador pronóstico y de respuesta al tratamiento en pacientes con ccRCC. La evidencia científica actual es limitada y son necesarios más estudios que demuestren su utilidad

Context and objective: There have been significant advances in the knowledge of renal carcinogenesis in the last years. Nowadays, renal tumours are classified according to their genetic profile and specific treatments based on the identification of therapeutic targets have also been developed. However, no prognostic markers have yet been identified. The aim of this review is to analyze literature that has evaluated the expression of the STAT3 protein as a molecular marker in clear cell renal carcinoma (ccRCC). Evidence acquisition: In January 2018 a systematic review was conducted in Pubmed, Cochrane library and Sciencedirect databases, from papers published from 1990. Search terms were "renal cell carcinoma" and "STAT3" or "STAT-3" and prognostic factor. Following the principles of the PRISMA declaration and the PICO selection strategy, original articles with series of patients diagnosed with localized or metastatic ccRCC, and where the activity of STAT3 is analyzed as a prognostic marker, were selected. A total of 132 publications were identified, of which 10 were finally revised, for they met the inclusion criteria. Evidence synthesis: STAT3 activation (phosphorylation) through Ser727 is important during ccRCC development and progression. PSTAT3 expression seems to be a prognostic marker and an antiangiogenic-resistance marker in metastatic patients. There is little evidence as prognostic marker in patients with localized disease. Conclusions: STAT3 (Ser 727) expression in the nucleus of the ccRCC cells can be a prognostic marker and an antiangiogenic-resistance marker. Current scientific evidence is limited and more studies are needed to demonstrate its usefulness

La resonancia magnética preoperatoria predice la recuperación temprana de la continencia urinaria tras la prostatectomía radical robótica / Preoperative magnetic resonance imaging in predicting early continence recovery after robotic radical prostatectomy

Introducción y objetivos: La incontinencia urinaria es una de las principales complicaciones tras la prostatectomía radical. El objetivo del estudio fue describir las características anatómicas, evaluadas preoperatoriamente mediante resonancia magnética, que permitan predecir la recuperación precoz de la continencia urinaria tras la prostatectomía radical asistida por robot. Material y métodos: Se analizó prospectivamente a 72 pacientes tratados mediante prostatectomía radical asistida por robot. Los resultados funcionales se evaluaron mediante los cuestionarios EPIC (1, 6 y 12 meses) y la fecha de primera continencia autoinformada. La longitud de la uretra membranosa (LUM) y el ángulo entre la LUM y el eje prostático (aLUMP) fueron evaluados preoperatoriamente en imágenes sagitales ponderadas en T2. Resultados: La tasa de continencia fue del 67,2, el 92,6 y el 95,2% a 1, 6 y 12 meses, respectivamente. Los pacientes con valores de aLUMP inferiores alcanzaron continencia urinaria temprana: al mes, los continentes habían tenido una aLUMP media de 107,21° (IC del 95% 90,3-124,6), mientras que entre los que presentaban incontinencia era de 118,5° (IC del 95% 117,7-134); p = 0,014. Hemos encontrado diferencias en el aLUMP entre los grupos según la continencia a los 6 meses: ángulo en continentes de 114,24° (IC del 95% 104,6-123,9), mientras que en los incontinentes había sido 142° (IC del 95% 126,5-157,6), p = 0,015. A los 12 meses, los continentes tenían una LUM preoperatoria significativamente superior a los incontinentes. En el análisis multivariante solamente el aLUMP fue un predictor independiente de continencia urinaria a los 6 meses OR 0,007 (IC del 95% 0,002-0,012), p = 0,012. Conclusiones: La evaluación de parámetros anatómicos preoperatorios previos a la cirugía puede ayudar a definir qué pacientes recuperarán la continencia urinaria precozmente, auxiliando a la toma de decisiones terapéuticas

Introduction and aims: Urinary incontinence is a common complication after radical prostatectomy. The aim of our study was to describe the preoperative anatomical features using magnetic resonance imaging in order to predict early continence recovery after robotic radical prostatectomy. Material and methods: 72 patients who underwent robotic radical prostatectomy were prospectively analysed. EPIC questionnaire (1, 6 and 12 mo) and first self-reported continence were used to assess functional outcomes. Membranous urethral length (MUL) and MUL-prostate axis angle (aMULP) were assessed preoperatively on T2 weighted sagittal images. Results: Continence rate was 67.2%, 92.6% and 95.2% at 1, 6 and 12 months, respectively. Early continence was achieved in patients with the lower aMULP. At 1 month, average aMULP in continent patients was 107.21° (CI 95% 90.3-124.6) vs. 118.5° (CI 95% 117.7-134) in incontinent ones (p = 0.014). At 6 month differences in aMULP among groups were found: 114.24° (CI 95% 104.6-123.9) in continents vs. 142° (CI 95% 126.5-157.6) in incontinents (p = 0.015). At 12 month, continent group showed a significantly higher preoperative aMULP. aMULP was revealed as the only independent predictor of urinary continence at 6 mo in multivariate analysis, OR 0.007 (CI 95% 0.002-0.012), p = 0.012. Conclusions: Preoperative anatomical parameters assessment prior surgery can help to identified those patients will achieve early continence recovery and it supports therapeutic decisions making

Preoperative magnetic resonance imaging in predicting early continence recovery after robotic radical prostatectomy. / La resonancia magnética preoperatoria predice la recuperación temprana de la continencia urinaria tras la prostatectomía radical robótica.

INTRODUCTION AND AIMS: Urinary incontinence is a common complication after radical prostatectomy. The aim of our study was to describe the preoperative anatomical features using magnetic resonance imaging in order to predict early continence recovery after robotic radical prostatectomy. MATERIAL AND METHODS: 72 patients who underwent robotic radical prostatectomy were prospectively analysed. EPIC questionnaire (1, 6 and 12 mo) and first self-reported continence were used to assess functional outcomes. Membranous urethral length (MUL) and MUL-prostate axis angle (aMULP) were assessed preoperatively on T2 weighted sagittal images. RESULTS: Continence rate was 67.2%, 92.6% and 95.2% at 1, 6 and 12 months, respectively. Early continence was achieved in patients with the lower aMULP. At 1 month, average aMULP in continent patients was 107.21° (IC 95% 90.3-124.6) vs. 118.5° (IC 95% 117.7-134) in incontinent ones (P=.014). At 6 month differences in aMULP among groups were found: 114.24° (IC 95% 104.6-123.9) in continents vs. 142° (IC 95% 126.5-157.6) in incontinents (P=0.015). At 12 month, continent group showed a significantly higher preoperative aMULP. aMULP was revealed as the only independent predictor of urinary continence at 6 mo in multivariate analysis, OR 0.007 (IC 95% 0.002-0.012), P=0.012. CONCLUSIONS: Preoperative anatomical parameters assessment prior surgery can help to identified those patients will achieve early continence recovery and it supports therapeutic decisions making.

The role of STAT3 protein as a prognostic factor in the clear cell renal carcinoma. Systematic review. / Valor de la proteína STAT3 como factor pronóstico en el carcinoma renal de célula clara. Revisión sistemática.

CONTEXT AND OBJECTIVE: There have been significant advances in the knowledge of renal carcinogenesis n the last years. Nowadays, renal tumors are classified according to their genetic profile and specific treatments based on the identification of therapeutic targets have also been developed. However, no prognostic markers have yet been identified. The aim of this review is to analyse literature that has evaluated the expression of the STAT3 protein as a molecular marker in clear cell renal carcinoma (ccRCC). EVIDENCE ACQUISITION: In January 2018 a systematic review was conducted in Pubmed, Cochrane library and Sciencedirect databases, from papers published from 1990. Search terms were"renal cell carcinoma"and"STAT3"or"STAT-3"and"prognostic factor. Following the principles of the PRISMA declaration and the PICO selection strategy, original articles with series of patients diagnosed with localized or metastatic ccRCC, and where the activity of STAT3 is analysed as a prognostic marker, were selected. A total of 132 publications were identified, of which 10 were finally revised, for they met the inclusion criteria. EVIDENCE SYNTHESIS: STAT3 activation (phosphorylation) through Ser727 is important during ccRCC development and progression. PSTAT3 expression seems to be a prognostic marker and an antiangiogenic-resistance marker in metastatic patients. There is little evidence as prognostic marker in patients with localized disease. CONCLUSIONS: STAT3 (Ser 727) expression in the nucleus of the ccRCC cells can be a prognostic marker and an antiangiogenic-resistance marker. Current scientific evidence is limited and more studies are needed to demonstrate its usefulness.

Radiofrecuencia percutánea guiada por ecografía en el tratamiento de masas renales pequeñas / Ultrasound-guided percutaneous radiofrequency ablation for treating small renal masses

Introducción: El objetivo del presente estudio ha sido analizar y evaluar la experiencia en ablación por radiofrecuencia de masas renales pequeñas mediante abordaje percutáneo guiado por ecografía con contraste en pacientes no aptos para la resección quirúrgica, y/o que no aceptaron vigilancia u observación. Material y método: Desde enero de 2007 hasta agosto de 2015 se han realizado 164 tratamientos en un total de 148 pacientes. Se presentan las características clínico-radiológicas de los pacientes, los resultados oncológicos y funcionales a corto y medio plazo. Resultados: La tasa de éxito técnico global fue del 97,5%, con éxito final en una sesión en el 100% de lesiones ≤ 3 cm y el 92% en lesiones entre 3-5 cm. El diámetro medio de los tumores en los que el tratamiento fue finalmente exitoso fue de 2,7 cm, mientras que el diámetro medio de estos fallos fue de 3,9 cm (p < 0,05). No se observaron diferencias estadísticamente significativas en la creatinina sérica y en el filtrado glomerular estimado. Conclusiones: A pesar de la baja tasa de biopsia renal positiva en la serie, la aplicación de radiofrecuencia percutánea ecoguiada en el tratamiento de lesiones renales pequeñas parece un procedimiento eficaz y seguro, con un mínimo impacto sobre la función renal, un aceptable control oncológico a corto y medio plazo, con una baja tasa de complicaciones

Introduction: The objective of this study was to analyse and assess the experience with radiofrequency ablation of small renal masses using a contrast-enhanced, ultrasound-guided percutaneous approach for patients who are not suitable for surgical resection and/or who refused surveillance or observation. Material and method: From January 2007 to August 2015, 164 treatments were performed on a total of 148 patients. We present the patients’ clinical-radiological characteristics, oncological and functional results in the short and medium term. Results: The overall technical success rate was 97.5%, with a successful outcome in 1 session in 100% of the lesions ≤ 3cm and 92% in lesions measuring 3-5cm. The mean tumour diameter in the patients for whom the treatment was ultimately successful was 2.7 cm, while the mean diameter of these in the unsuccessful operations was 3.9 cm (P < .05). There were no statistically significant differences in the serum creatinine levels and estimated glomerular filtration rates. Conclusions: Despite the low rate of positive renal biopsies in the series, ultrasound-guided percutaneous radiofrequency ablation for treating small renal lesions appears to be an effective and safe procedure with a minimum impact on renal function, an acceptable oncologic control in the short and medium term and a low rate of complications

Ultrasound-guided percutaneous radiofrequency ablation for treating small renal masses. / Radiofrecuencia percutánea guiada por ecografía en el tratamiento de masas renales pequeñas.

INTRODUCTION: The objective of this study was to analyse and assess the experience with radiofrequency ablation of small renal masses using a contrast-enhanced, ultrasound-guided percutaneous approach for patients who are not suitable for surgical resection and/or who refused surveillance or observation. MATERIAL AND METHOD: From January 2007 to August 2015, 164 treatments were performed on a total of 148 patients. We present the patients' clinical-radiological characteristics, oncological and functional results in the short and medium term. RESULTS: The overall technical success rate was 97.5%, with a successful outcome in 1 session in 100% of the lesions≤3cm and 92% in lesions measuring 3-5cm. The mean tumour diameter in the patients for whom the treatment was ultimately successful was 2.7cm, while the mean diameter of these in the unsuccessful operations was 3.9cm (P<.05). There were no statistically significant differences in the serum creatinine levels and estimated glomerular filtration rates. CONCLUSIONS: Despite the low rate of positive renal biopsies in the series, ultrasound-guided percutaneous radiofrequency ablation for treating small renal lesions appears to be an effective and safe procedure with a minimum impact on renal function, an acceptable oncologic control in the short and medium term and a low rate of complications.

Revisión sistemática de los factores pronósticos del carcinoma renal / Systematic review of renal carcinoma prognostic factors

Contexto y objetivo: La evolución natural del carcinoma renal es heterogénea, encontrando diversos escenarios en cuanto a la presentación clínica, evolución y tipo de recidiva (local/metastásica). El objetivo de esta publicación es revisar la literatura existente con relación a los principales factores pronósticos del carcinoma renal. Adquisición de evidencia Se realiza una revisión sistemática mediante Pubmed de los artículos publicados, de acuerdo con los principios de la declaración PRISMA, desde 1999 (primera publicación de la clasificación de Motzer) hasta 2015. Los términos utilizados en la búsqueda han sido «kidney neoplasms», «kidney cancer», «renal cell carcinoma», «prognostic factors», «mortality», «survival» y «disease progression». Síntesis de evidencia: El mejor conocimiento de las vías moleculares implicadas en la oncogénesis renal junto con la aparición de tratamientos dirigidos con nuevas moléculas están provocando que los antiguos modelos pronósticos queden obsoletos, requiriendo de una revisión continua para la actualización de los nomogramas disponibles adaptados a los nuevos escenarios. Conclusiones: Es importante una correcta validación externa de los factores pronósticos existentes mediante estudios prospectivos y multicéntricos, para poder así incorporarlos a la práctica clínica habitual del urólogo

Context and objectives: The natural history of renal cell carcinoma is heterogeneous. Some scenarios can be found in terms of clinical presentation, clinical evolution or type of recurrence (local/metastatic). The aim of this publication is to analyze the most important prognostic factors published in the literature. Evidence acquisition: A literature review ob published papers was performed using the Pubmed, from first Motzer's classification published in 1999 to 2015, according to PRISMA declaration. Search was done using the following keywords: kidney neoplasm, kidney cancer, renal cell carcinoma, prognostic factors, mortality, survival and disease progression. Papers were classified according to level of evidence, the number of patients included and the type of study performed. Evidence synthesis: The evolution in the knowledge of molecular pathways related to renal oncogenesis and the new targeted therapies has left to remain obsolete the old prognostic models. It's necessary to perform a continuous review to actualize nomograms and to adapt them to the new scenarios. Conclusions: Is necessary to perform a proper external validation of existing prognostic factors using prospective and multicentric studies to add them into the daily urologist clinical practice

Systematic review of renal carcinoma prognostic factors. / Revisión sistemática de los factores pronósticos del carcinoma renal.

CONTEXT AND OBJECTIVES: The natural history of renal cell carcinoma is heterogeneous. Some scenarios can be found in terms of clinical presentation, clinical evolution or type of recurrence (local/metastatic). The aim of this publication is to analyze the most important prognostic factors published in the literature. EVIDENCE ACQUISITION: A literature review ob published papers was performed using the Pubmed, from first Motzer's classification published in 1999 to 2015, according to PRISMA declaration. Search was done using the following keywords: kidney neoplasm, kidney cancer, renal cell carcinoma, prognostic factors, mortality, survival and disease progression. Papers were classified according to level of evidence, the number of patients included and the type of study performed. EVIDENCE SYNTHESIS: The evolution in the knowledge of molecular pathways related to renal oncogenesis and the new targeted therapies has left to remain obsolete the old prognostic models. It's necessary to perform a continuous review to actualize nomograms and to adapt them to the new scenarios. CONCLUSIONS: Is necessary to perform a proper external validation of existing prognostic factors using prospective and multicentric studies to add them into the daily urologist clinical practice.

Cambios hormonales después del tratamiento de cáncer de próstata localizado. Comparación entre radioterapia de haz externo y prostatectomía radical / Hormonal changes after localized prostate cancer treatment. Comparison between external beam radiation therapy and radical prostatectomy

Objetivos: Determinar la influencia de la prostatectomía radical (PR) y de la radioterapia externa (RT) sobre el eje hipotálamo-hipofisario de 120 pacientes con cáncer de próstata clínicamente localizado tratados con PR o RT exclusiva. Material y métodos: Estudiamos 120 pacientes con cáncer de próstata localizado. Noventa y dos pacientes recibieron PR y 28 RT exclusiva. Medimos los niveles séricos de hormona luteinizante, hormona folículo estimulante (FSH), testosterona total (T), testosterona libre y estradiol basalmente y a los 3 y 12 meses tras completar el tratamiento. Resultados: Los pacientes sometidos a PR eran más jóvenes y presentaban mayor volumen prostático (64,3 vs. 71,1 años, p < 0,0001 y 55,1 vs. 36,5 g, p < 0,0001; respectivamente). No encontramos diferencias en los niveles hormonales basales. Los niveles de hormona luteinizante y FSH eran significativamente superiores en los pacientes tratados con RT a los 3 meses (hormona luteinizante 8,54 vs. 4,76 U/l, FSH 22,96 vs. 8,18 U/l, p < 0,0001) y los niveles de T y testosterona libre significativamente inferiores (T 360,3 vs. 414,83 ng/dl, p 0,039; FT 5,94 vs. 7,5 pg/ml, p 0,018). A los 12 meses los niveles de FSH permanecían significativamente superiores en los pacientes tratados con RT comparado con pacientes tratados con PR (21,01 vs. 8,51 U/l, p < 0,001) y los niveles de T permanecían significativamente inferiores (339,89 vs. 402,39 ng/dl, p 0,03). Conclusiones: El tratamiento del cáncer de próstata influye en el eje hipotálamo-hipofisario. La influencia parece más importante en los pacientes tratados con RT. Necesitamos más estudios que eluciden el papel que la próstata puede jugar como órgano endocrino

Objective: To determine the influence of radical prostatectomy (RP) and external beam radiation therapy (EBRT) on the hypothalamic pituitary axis of 120 men with clinically localized prostate cancer treated with RP or EBRT exclusively. Materials and methods: 120 patients with localized prostate cancer were enrolled. Ninety two patients underwent RP and 28 patients EBRT exclusively. We measured serum levels of luteinizing hormone, follicle stimulating hormone (FSH), total testosterone (T), free testosterone, and estradiol at baseline and at 3 and 12 months after treatment completion. Results: Patients undergoing RP were younger and presented a higher prostate volume (64.3 vs. 71.1 years, p < 0.0001 and 55.1 vs. 36.5 g, p < 0.0001; respectively). No differences regarding serum hormonal levels were found at baseline. Luteinizing hormone and FSH levels were significantly higher in those patients treated with EBRT at three months (luteinizing hormone 8,54 vs. 4,76 U/l, FSH 22,96 vs. 8,18 U/l, p < 0,0001) while T and free testosterone levels were significantly lower (T 360,3 vs. 414,83 ng/dl, p 0,039; free testosterone 5,94 vs. 7,5 pg/ml, p 0,018). At 12 months FSH levels remained significantly higher in patients treated with EBRT compared to patients treated with RP (21,01 vs. 8,51 U/l, p < 0,001) while T levels remained significantly lower (339,89 vs. 402,39 ng/dl, p 0,03). Conclusions: Prostate cancer treatment influences the hypothalamic pituitary axis. This influence seems to be more important when patients with prostate cancer are treated with EBRT rather than RP. More studies are needed to elucidate the role that prostate may play as an endocrine organ

Eficacia del índice de salud prostática para identificar cánceres de próstata agresivos. Una validación institucional / Diagnostic accuracy of prostate health index to identify aggressive prostate cancer. An Institutional validation study

Introducción: Las nuevas generaciones de marcadores tumorales para diagnosticar precozmente el cáncer de próstata (CaP) deberían ser capaces de discriminar entre pacientes portadores de tumores agresivos y aquellos sin cáncer, o con tumores de baja agresividad. El objetivo de este estudio ha sido validar en una institución académica el índice de salud prostática (PHI) como marcador de tumores agresivos de próstata. Métodos: Se determinó PHI en 357 varones sometidos a biopsia prostática entre junio de 2013 y julio de 2014. Posteriormente, un subgrupo de 183 hombres menores de 75 años, con PSA entre 3,0 y 10,0 ng/ml y programados para su primera biopsia fue seleccionado para este estudio. En todos ellos se llevó a cabo una biopsia prostática transrectal, guiada por ultrasonidos y bajo anestesia local, que obtuvo 12 cilindros de la zona periférica. En todos los casos se determinó antes del procedimiento: PSA total (tPSA), PSA libre (fPSA), [-2] proPSA (p2PSA) y volumen prostático. Se calculó el porcentaje de fPSA (%fPSA), densidad de PSA (PSAd) y PHI. Se consideraron tumores agresivos aquellos que tuvieron algún patrón 4 en la biopsia. Se comparó PHI con %fPSA y PSAd a través del análisis de curvas ROC. Se establecieron dinteles para detectar el 90% y el 95% de todos los tumores y el 95% y el 100% de los tumores agresivos, y se calcularon las tasas de biopsias evitadas con cada uno de ellos. Resultados: La tasa global de detección de CaP fue del 37,2% y la de tumores agresivos del 24,6%. El área bajo la curva (AUC) de PHI para detectar cualquier tipo de tumor fue superior a la de %fPSA y PSAd (0,749 vs 0,606 y 0,668 respectivamente). De forma similar, cuando se consideraron solo los tumores agresivos las AUC fueron respectivamente 0,786 vs 0,677 y 0,708. La tasa de biopsias evitadas para detectar el 95% de los tumores agresivos fue del 20,2% para PHI, 14,8% para %fPSA y 23,5% para PSAd. Para detectar el 100% de tumores agresivos la tasa de biopsias evitadas cayó al 5,9% para PHI, 9,3% para %fPSA y 7,9% para PSAd. Conclusiones: PHI parece un buen marcador para diagnosticar el CaP. Sin embargo, cuando el objetivo es detectar al menos el 95% de los tumores agresivos no parece ser más eficaz que el %fPSA y la PSAd

Introduction: New generations of tumor markers used to detect prostate cancer (PCa) should be able to discriminate men with aggressive PCa of those without PCa or nonaggressive tumors. The objective of this study has been to validate Prostate Health Index (PHI) as a marker of aggressive PCa in one academic institution. Methods: PHI was assessed in 357 men scheduled to prostatic biopsy between June of 2013 and July 2014 in one academic institution. Thereafter a subset of 183 men younger than 75 years and total PSA (tPSA) between 3.0 and 10.0 ng/mL, scheduled to it first prostatic biopsy, was retrospectively selected for this study. Twelve cores TRUS guided biopsy, under local anaesthesia, was performed in all cases. Total PSA, free PSA (fPSA), and [-2] proPSA (p2PSA) and prostate volume were determined before the procedure and %fPSA, PSA density (PSAd) and PHI were calculated. Aggressive tumors were considered if any Gleason 4 pattern was found. PHI was compared to %fPSA and PSAd through their ROC curves. Thresholds to detect 90%, 95% of all tumors and 95% and 100% of aggressive tumors were estimated and rates of unnecessary avoided biopsies were calculated and compared. Results: The rate of PCa detection was 37.2% (68) and the rate of aggressive tumors was 24.6% (45). The PHI area under the curve was higher than those of %fPSA and PSAd to detect any PCa (0.749 vs 0.606 and 0.668 respectively) or to detect only aggressive tumors (0.786 vs 0.677 and 0.708 respectively), however, significant differences were not found. The avoided biopsy rates to detect 95% of aggressive tumors were 20.2% for PHI, 14.8% for %fPSA, and 23.5% for PSAd. Even more, to detect all aggressive tumors these rates dropped to 4.9% for PHI, 9.3% for %fPSA, and 7.9% for PSAd. Conclusions: PHI seems a good marker to PCa diagnosis. However, PHI was not superior to %fPSA and PSAd to identify at least 95% of aggressive tumors

Hormonal changes after localized prostate cancer treatment. Comparison between external beam radiation therapy and radical prostatectomy. / Cambios hormonales después del tratamiento de cáncer de próstata localizado. Comparación entre radioterapia de haz externo y prostatectomía radical.

OBJECTIVE: To determine the influence of radical prostatectomy (RP) and external beam radiation therapy (EBRT) on the hypothalamic pituitary axis of 120 men with clinically localized prostate cancer treated with RP or EBRT exclusively. MATERIALS AND METHODS: 120 patients with localized prostate cancer were enrolled. Ninety two patients underwent RP and 28 patients EBRT exclusively. We measured serum levels of luteinizing hormone, follicle stimulating hormone (FSH), total testosterone (T), free testosterone, and estradiol at baseline and at 3 and 12 months after treatment completion. RESULTS: Patients undergoing RP were younger and presented a higher prostate volume (64.3 vs. 71.1 years, p<0.0001 and 55.1 vs. 36.5 g, p<0.0001; respectively). No differences regarding serum hormonal levels were found at baseline. Luteinizing hormone and FSH levels were significantly higher in those patients treated with EBRT at three months (luteinizing hormone 8,54 vs. 4,76 U/l, FSH 22,96 vs. 8,18 U/l, p<0,0001) while T and free testosterone levels were significantly lower (T 360,3 vs. 414,83ng/dl, p 0,039; free testosterone 5,94 vs. 7,5pg/ml, p 0,018). At 12 months FSH levels remained significantly higher in patients treated with EBRT compared to patients treated with RP (21,01 vs. 8,51 U/l, p<0,001) while T levels remained significantly lower (339,89 vs. 402,39ng/dl, p 0,03). CONCLUSIONS: Prostate cancer treatment influences the hypothalamic pituitary axis. This influence seems to be more important when patients with prostate cancer are treated with EBRT rather than RP. More studies are needed to elucidate the role that prostate may play as an endocrine organ.

Diagnostic accuracy of prostate health index to identify aggressive prostate cancer. An Institutional validation study. / Eficacia del índice de salud prostática para identificar cánceres de próstata agresivos. Una validación institucional.

INTRODUCTION: New generations of tumor markers used to detect prostate cancer (PCa) should be able to discriminate men with aggressive PCa of those without PCa or nonaggressive tumors. The objective of this study has been to validate Prostate Health Index (PHI) as a marker of aggressive PCa in one academic institution. METHODS: PHI was assessed in 357 men scheduled to prostatic biopsy between June of 2013 and July 2014 in one academic institution. Thereafter a subset of 183 men younger than 75 years and total PSA (tPSA) between 3.0 and 10.0 ng/mL, scheduled to it first prostatic biopsy, was retrospectively selected for this study. Twelve cores TRUS guided biopsy, under local anaesthesia, was performed in all cases. Total PSA, free PSA (fPSA), and [-2] proPSA (p2PSA) and prostate volume were determined before the procedure and %fPSA, PSA density (PSAd) and PHI were calculated. Aggressive tumors were considered if any Gleason 4 pattern was found. PHI was compared to %fPSA and PSAd through their ROC curves. Thresholds to detect 90%, 95% of all tumors and 95% and 100% of aggressive tumors were estimated and rates of unnecessary avoided biopsies were calculated and compared. RESULTS: The rate of PCa detection was 37.2% (68) and the rate of aggressive tumors was 24.6% (45). The PHI area under the curve was higher than those of %fPSA and PSAd to detect any PCa (0.749 vs 0.606 and 0.668 respectively) or to detect only aggressive tumors (0.786 vs 0.677 and 0.708 respectively), however, significant differences were not found. The avoided biopsy rates to detect 95% of aggressive tumors were 20.2% for PHI, 14.8% for %fPSA, and 23.5% for PSAd. Even more, to detect all aggressive tumors these rates dropped to 4.9% for PHI, 9.3% for %fPSA, and 7.9% for PSAd. CONCLUSIONS: PHI seems a good marker to PCa diagnosis. However, PHI was not superior to %fPSA and PSAd to identify at least 95% of aggressive tumors.

Simultaneous treatment with statins and aspirin reduces the risk of prostate cancer detection and tumorigenic properties in prostate cancer cell lines.

Nowadays prostate cancer is the most common solid tumor in men from industrialized countries and the second leading cause of death. At the ages when PCa is usually diagnosed, mortality related to cardiovascular morbidity is high; therefore, men at risk for PCa frequently receive chronic lipid-lowering and antiplatelet treatment. The aim of this study was to analyze how chronic treatment with statins, aspirin, and their combination influenced the risk of PCa detection. The tumorigenic properties of these treatments were evaluated by proliferation, colony formation, invasion, and migration assays using different PCa cell lines, in order to assess how these treatments act at molecular level. The results showed that a combination of statins and aspirin enhances the effect of individual treatments and seems to reduce the risk of PCa detection (OR: 0.616 (95% CI: 0.467-0.812), P<0.001). However, if treatments are maintained, aspirin (OR: 1.835 (95% CI: 1.068-3.155), P=0.028) or the combination of both drugs (OR: 3.059 (95% CI: 1.894-4.939), P<0.001) represents an increased risk of HGPCa. As observed at clinical level, these beneficial effects in vitro are enhanced when both treatments are administered simultaneously, suggesting that chronic, concomitant treatment with statins and aspirin has a protective effect on PCa incidence.

Ureteropielostomía con vía nativa en el tratamiento de la uropatía obstructiva en el trasplante renal adulto. Experiencia y posibilidades técnicas / Native ureteropyelostomy in the treatment of obstructive uropathy in adult renal transplant. Experience and technical alternatives

Objetivo: Analizar y evaluar nuestra experiencia en el tratamiento quirúrgico mediante abordaje abierto de las estenosis ureterales complejas postrasplante renal de adulto en un centro de tercer nivel en los últimos 7 años. Se revisan las diferentes alternativas quirúrgicas utilizadas. Pacientes y métodos: Desde enero de 2005 hasta diciembre de 2012 se han realizado un total de 589 trasplantes renales de adulto consecutivos. Un 1,1% del total presentaron algún grado de uropatía obstructiva sintomática que, tras derivación urinaria inicial, requirieron de abordaje quirúrgico abierto utilizando la vía urinaria nativa ipsilateral o contralateral. Se presentan las características de los pacientes, clínica, exploraciones realizadas así como técnica quirúrgica llevada a cabo y sus resultados. Resultados: Durante el periodo evaluado se llevaron a cabo un total de 7 cirugías reparativas en 5 varones y 2 mujeres que presentaban estenosis ureterales postrasplante renal mediante ureteropielostomía abierta utilizando uréter nativo ipsilateral en 6 casos y contralateral en el restante. En un caso de realizó anastomosis ureterocalicilar por retracción piélica extrema. No ha habido complicaciones relevantes ni se ha requerido de nefrectomía de riñón nativo por complicación posterior. La totalidad de los pacientes intervenidos presentaron cifras de creatinina plasmática óptimas con resolución de la dilatación previa. Conclusiones: La nefrostomía percutánea inicial seguida de la corrección quirúrgica abierta mediante la utilización de uréter nativo representa una alternativa definitiva, válida y óptima en términos de seguridad y preservación de la función renal

Objective: To analyze and evaluate our experience in surgical treatment with the open approach of the complex ureteral stenosis after adult kidney transplantation in a tertiary level hospital in the last seven years. We have reviewed the different surgical options used. Patients and methods: A total of 589 consecutive adult renal transplants were performed from January 2005 to December 2012. Of these, 1.1% showed some degree of symptomatic obstructive uropathy which after initial urinary diversion required open surgical approach using the ipsilateral or contralateral native urinary tract. Characteristics of the patient, clinical examinations performed and surgical technique performed as well as their results are presented. Results: During the period under review, in 5 men and 2 women who had ureteral stenoses after renal transplant, 7 reparative surgeries were performed by open ureteropyelostomy, using ipsilateral native ureter in 6 cases and contralateral ureter in the remaining case. In one case, uretero-calicial anastomosis was performed due to severe pyelic shrinkage. There were no significant complications. Native kidney nephrectomy was not required for further complications. All the patients operated on had optimum plasma creatinine levels with resolution of previous dilatation. Conclusions: The initial percutaneous nephrostomy followed by open surgical repair using native ureter represents a definitive, valid and optimal alternative in terms of safety and preservation of renal function

Síndrome metabólico en pacientes con cáncer de próstata sometidos a supresión androgénica / Metabolic syndrome in patients with prostate cancer undergoing androgen suppression

Objetivos: La mortalidad cardiovascular es la primera causa de muerte en pacientes con cáncer de próstata (CP) y el síndrome metabólico (SM) está relacionado con ella. El objetivo principal de este estudio fue conocer la prevalencia del SM en pacientes con CP sometidos a supresión androgénica (SA). Material y métodos: Se realizó un estudio retrospectivo de casos y controles que incluyó 159 pacientes. Cincuenta y tres pacientes con CP sometidos a SA durante un periodo superior a 12 meses formaron el grupo de casos; 53 pacientes con CP en el momento de su diagnóstico y 53 pacientes con biopsia prostática negativa formaron el grupo control. En todos los pacientes se evaluó la existencia de SM según los criterios del NCEP-ATPIII. Resultados: La prevalencia de SM en pacientes sin CP fue del 32,1% y en pacientes con CP no tratados fue del 35,8%; p = 0,324. En pacientes con CP sometidos a SA la prevalencia de SM fue del 50,9%; p < 0,001. Cuando la SA fue inferior a 36 meses se observó una prevalencia del 44,0% y cuando fue superior o igual a 36 meses del 57,1%; p < 0,001. El perímetro abdominal (> 102 cm) y la hiperglucemia (> 110 mg/dl) fueron los 2 componentes del SM que se incrementaron significativamente. La SA y su duración fueron factores predictores independientes del desarrollo de SM. Conclusiones: La SA continuada incrementa la prevalencia de SM y especialmente el perímetro abdominal y la hiperglucemia. Su desarrollo aumenta con la duración de la SA

Objectives: Cardiovascular mortality is the leading cause of death in patients with prostate cancer (PC), metabolic syndrome (MS) being related to it. The main objective of this study was to determine the prevalence of MS in patients with CP undergoing androgen suppression (AS). Materials and methods: We performed a retrospective study of cases and controls that included 159 patients. The study group was made up of 53 patients with PC undergoing SA for a period exceeding 12 months. The control group had 53 patients with PC at the time of diagnosis and 53 patients with negative prostate biopsy. All the patients were evaluated for presence of MS according to NCEP-ATPIII criteria. Results: Prevalence of MS in patients without PC was 32.1% and in those with non-treated PC 35.8%, P = 0.324. In patients with PC undergoing AS, prevalence of MS was 50.9%, P < 0.001. When AS duration was less than 36 months, prevalence of MS was 44.0% and when greater than 36 months 57.1%, P < 0.001. Waist circumference and hyperglycemia were the two MS components that significantly increased. AS and its duration were independent predictors factors for the development of MS. Conclusions: Continuous AS therapy increases the prevalence of MS and especially waist circumference and hyperglycemia. Development of MS increases according to AS duration

Sedentarismo y sobrepeso como factores de riesgo en la detección del cáncer de próstata y su agresividad / Sedentarism and overweight as risk factors for the detection of prostate cancer and its aggressivenes

Objetivo: Analizar la influencia del sedentarismo (SE) y sobrepeso (SP) en el riesgo de detección de cáncer de próstata (CP) y su agresividad. Material y método: Se realizó biopsia prostática (BP) a 2.408 varones consecutivos, no tratados con 5 ARI, a causa de elevación sérica del PSA por encima de 4,0 ng/ml (91%) o tacto rectal sospechoso (9%). En la BP, transrectal y ecodirigida, se obtuvieron 10 cilindros, y entre 2 y 8 adicionales en función de la edad y del volumen prostático. La actividad física se evaluó mediante una encuesta (SE vs no SE) y se calculó el índice de masa corporal (normal vs SP: > 25 kg/cm2). La agresividad tumoral se evaluó según la suma de Gleason (alto grado [AG]: Gleason > 7) y el riesgo de D'Amico (alto riesgo [AR]: T > 3a o PSA > 20 o suma de Gleason > 7). Resultados: Se halló una asociación significativa entre SE (52,5%) y SP (72,9%), p > 0,001. La tasa global de detección de CP fue 35,2%. En varones con SE fue 36,7% y en no SE 33,6%, p = 0,048. La tasa global de tumores de AG fue 28,3%, 29,2% en varones con SE y 27,1% en no SE, p = 0,261. La tasa global de tumores de AR fue 35%, 39,7% en varones con SE y 29,4% en no SE, p < 0,001. Se detectó CP en un 38,1% de hombres con IMC normal y 34,3% en hombres con SP, p = 0,065. La tasa de tumores de AG fue 18,1 y 31,4% respectivamente, p < 0,001, y la tasa de tumores de AR fue 22,6 y 39,2% respectivamente, p < 0,001. La regresión logística binaria mostró que el SE fue un predictor independiente de CP, RR 0,791 (95% IC: 0,625-0,989), p = 0,030. SE y SP fueron predictores independientes de AG: RR 0,517 (95% IC: 0,356-0,752), p = 0,001, y RR 1,635 (95% IC 1,070-2,497), p = 0,023. SE y SP también fueron predictores independientes de AR: RR 0,519 (95% IC: 0,349-0,771), p = 0,001, y RR 1,998 (95% IC: 1,281-3,115), p = 0,002. Conclusiones: En varones que cumplen criterios de biopsia prostática se encontró una asociación entre sedentarismo y sobrepeso. El sedentarismo se asoció a mayor riesgo de detección de CP, mientras sedentarismo y sobrepeso incrementaron el riesgo de detección de tumores más agresivos

Objective: To analyze the influence of sedentary (SE) and overweight (OW) in the risk of prostate cancer detection (CP) and aggressiveness. Material and method: We performed prostate biopsy (PB) to 2,408 consecutive male, 5 ARIs untreated, because of elevated serum PSA above 4.0 ng/mL (91%) or suspicious digital rectal examination (9%). In all ultrasound guided PB, 10 cores were obtained plus 2 to 8 additionals, according to age and prostate volume. Physical activity was assessed using a survey (SE vs non-SE) and calculated body mass index (normal vs OW > 25 kg/cm2). The tumor aggressiveness was evaluated according to the Gleason score (high grade «HG»: Gleason> 7) and D’Amico risk (high risk «HR»: T > 3a or PSA > 20 or Gleason score > 7). Results: We found a significant association between SE (52.5%) and OW (72.9%), P < 0.001. The overall PC detection rate was 35.2%. In men with SE it was 36.7% and non-SE 33.6%, P = 0.048. The overall rate of AG tumors was 28.3%, 29.2% in men with SE and 27.1 in non-SE, P = 0.261. The overall rate of AR tumors was 35%, 39.7% in men with SE and 29.4% non-SE, P < 0.001. CP was detected in 38.1% of men with normal BMI and 34.3% in men with OW, P = 0.065. HG tumor rates were 18.1% and 31.4% respectively, P < 0.001 and AR tumor rates were 22.6% and 39.2% respectively, P < 0.001. Binary logistic regression showed that SE was an independent predictor of CP, OR .791 (95% CI: .625-0.989), P = 0.030. SE and OW were independent predictors of HG: OR .517 (95% CI: .356-0.752), P = 0.001, and OR 1.635 (95% CI: 1070-2497), p = 0.023. SE and OW were also independent predictors of HR: OR 0.519 (95% CI 0.349-.771), P = 0.001, and OR 1.998 (95% CI 1.281-3.115), P = 0.002. Conclusions: In men who met criteria for prostate biopsy an association between sedentary and overweight exist. A sedentary lifestyle is associated with increased risk of PC detection while sedentary and overweight were associated with more aggressive tumors