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1.
Article in English, Spanish | MEDLINE | ID: mdl-38734069

ABSTRACT

INTRODUCTION: The prevalence of endometriosis is estimated to be about 10% among women of reproductive age. In about 5-10% of these patients, involvement of urological structures will be developed due to deep endometriosis. Urologists should be familiar with the management of these patients, who will require multidisciplinary care with medical and surgical treatment. MATERIAL AND METHODS: Retrospective study of patients diagnosed with deep endometriosis involving urological structures who underwent surgery performed jointly with gynecology and colorectal surgery departments from June 2012 until June 2021 (60 cases). Urologic symptoms were grouped into 3 groupers for subsequent analysis (storage symptoms, voiding symptoms, and low back pain). RESULTS: Storage symptoms (frequency and urgency) are the most frequent urologic symptoms. Patients with storage symptoms and low back pain showed improvement after surgery. In contrast, patients with voiding symptoms did not improve with surgical treatment. CONCLUSIONS: The prevalence of endometriosis and the likelihood of involving urologic structures require the urologic community to be aware of the pathology. Patients with storage symptoms will improve following excision of the endometriotic nodules. The need for Partial cystectomies with ureteral reimplantation can be safely performed by laparoscopic or robotic approach, even in previously operated patients, without compromising long-term function.

2.
Article in English, Spanish | MEDLINE | ID: mdl-38740264

ABSTRACT

INTRODUCTION AND OBJECTIVE: Robotic-assisted laparoscopic prostatectomy (PLAR) seems to improve functional outcomes, however there is not a consensus of a standard procedure. The aim of this study was to identify the PLAR "state of art" in Catalonia, Spain. MATERIAL AND METHODS: This was a cross-sectional survey-based study conducted among urologists across Catalonia, Spain. The survey was distributed through online platforms and the professional urology society. All statistical analyses were performed using Stata software, v20. RESULTS: 59 urologists completed the survey, revealing PLAR as the most commonly used technique (79.7%). Most urologist (70%) create the pneumoperitoneum using a controlled incision with direct access and 78.3% use the Airseal technology. The intraperitoneal approach is performed in >90% of cases. Endopelvic fascia preservation is not routinely performed. 34.5% of the survey not perform the dorsal vein complex suture. All preserves the bladder neck when oncologically safe. Nerve-vascular bundles bleeding control is performed using standard coagulation or suturing. 34% performed posterior reconstruction. Only use hemostatic devices when evident bleeding and 70% does not routinely left a drainage. Multivariable analysis showed that center volume had a significant independent association with dorsal venous complex suturing (OR 0.073, 95%CI 0.07-0.826), nerve-vascular bundles suturing hemostasis (OR 11.67, 95%CI 1.07-127.60) and endopelvic fascia preservation (OR 13.64, 95%CI 1.087-201.27), but there was no correlation with time the bladder catheter or days hospitalized. CONCLUSIONS: The study provides an overview of the state of PLAR in Catalonia, Spain, showing significant variability and reflecting a commitment to advancing surgical technology and patient care.

3.
Ann Oncol ; 35(5): 458-472, 2024 May.
Article in English | MEDLINE | ID: mdl-38417742

ABSTRACT

BACKGROUND: Although germline BRCA mutations have been associated with adverse outcomes in prostate cancer (PC), understanding of the association between somatic/germline alterations in homologous recombination repair (HRR) genes and treatment outcomes in metastatic castration-resistant PC (mCRPC) is limited. The aim of this study was to investigate the prevalence and outcomes associated with somatic/germline HRR alterations, particularly BRCA1/2, in patients initiating first-line (1L) mCRPC treatment with androgen receptor signalling inhibitors (ARSi) or taxanes. PATIENTS AND METHODS: Data from 729 mCRPC patients were pooled for CAPTURE from four multicentre observational studies. Eligibility required 1L treatment with ARSi or taxanes, adequate tumour samples and biomarker panel results. Patients underwent paired normal and tumour DNA analyses by next-generation sequencing using a custom gene panel including ATM, BRCA1, BRCA2, BRIP1, CDK12, CHEK2, FANCA, HDAC2, PALB2, RAD51B and RAD54L. Patients were divided into subgroups based on somatic/germline alteration(s): with BRCA1/2 mutations (BRCA); with HRR mutations except BRCA1/2 (HRR non-BRCA); and without HRR alterations (non-HRR). Patients without BRCA1/2 mutations were classified as non-BRCA. Radiographic progression-free survival (rPFS), progression-free survival 2 (PFS2) and overall survival (OS) were assessed. RESULTS: Of 729 patients, 96 (13.2%), 127 (17.4%) and 506 (69.4%) were in the BRCA, HRR non-BRCA and non-HRR subgroups, respectively. BRCA patients performed significantly worse for all outcomes than non-HRR or non-BRCA patients (P < 0.05), while PFS2 and OS were significantly shorter for BRCA than HRR non-BRCA patients (P < 0.05). HRR non-BRCA patients also had significantly worse rPFS, PFS2 and OS than non-HRR patients. Exploratory analyses suggested that for BRCA patients, there were no significant differences in outcomes associated with 1L treatment choice (ARSi or taxanes) or with the somatic/germline origin of the alterations. CONCLUSIONS: Worse outcomes were observed for mCRPC patients in the BRCA subgroup compared with non-BRCA subgroups, either HRR non-BRCA or non-HRR. Despite its heterogeneity, the HRR non-BRCA subgroup presented worse outcomes than the non-HRR subgroup. Screening early for HRR mutations, especially BRCA1/2, is crucial in improving mCRPC patient prognosis.


Subject(s)
Germ-Line Mutation , Prostatic Neoplasms, Castration-Resistant , Recombinational DNA Repair , Humans , Male , Prostatic Neoplasms, Castration-Resistant/genetics , Prostatic Neoplasms, Castration-Resistant/drug therapy , Prostatic Neoplasms, Castration-Resistant/pathology , Prostatic Neoplasms, Castration-Resistant/mortality , Aged , Recombinational DNA Repair/genetics , Middle Aged , BRCA2 Protein/genetics , Aged, 80 and over , Taxoids/therapeutic use , BRCA1 Protein/genetics , Androgen Receptor Antagonists/therapeutic use , Biomarkers, Tumor/genetics , Progression-Free Survival , Mutation
7.
Clin. transl. oncol. (Print) ; 23(5): 969-979, mayo 2021. tab
Article in English | IBECS | ID: ibc-221237

ABSTRACT

The treatment of advanced prostate cancer has evolved due to recent advances in molecular research and new drug development. Dynamic aberrations in the androgen receptor, DNA repair genes, PTEN-PI3K, and other pathways drive the behavior of advanced prostate cancer allowing a better selection of therapies in each patient. Tumor testing for BRCA1 and BRCA2 is recommended for patients with metastatic prostate cancer, also considering a broad panel to guide decisions and genetic counseling. In symptomatic metastatic patients, castration should be stared to palliate symptoms and prolong survival. In high-risk or high-volume metastatic hormone-naïve patients, castration should be combined with docetaxel, abiraterone, enzalutamide or apalutamide. Radiotherapy to the primary tumor combined with systemic therapy is recommended in low-volume mHNPC patients. In patients with non-metastatic castration-resistant tumors, risk stratification can define the frequency of imaging. Adding enzalutamide, darolutamide or apalutamide to these patients prolongs metastasis-free and overall survival, but potential adverse events need to be taken into consideration. The choice of docetaxel, abiraterone or enzalutamide for treating metastatic castration-resistant patients depends on previous therapies, with cabazitaxel being also recommended after docetaxel. Olaparib is recommended in BRCA1/BRCA2 mutated castration-resistant patients after progression on at least one new hormonal therapy. Aggressive variants of prostate cancer respond to platinum-based chemotherapy. To optimize treatment efficiency, oncologists should incorporate all of these advances into an overall therapeutic strategy (AU)


Subject(s)
Humans , Male , Prostatic Neoplasms/diagnosis , Prostatic Neoplasms/therapy , Neoplasm Staging , Biomarkers, Tumor , Genetic Markers , Societies, Medical , Spain
8.
Clin Transl Oncol ; 23(5): 969-979, 2021 May.
Article in English | MEDLINE | ID: mdl-33625671

ABSTRACT

The treatment of advanced prostate cancer has evolved due to recent advances in molecular research and new drug development. Dynamic aberrations in the androgen receptor, DNA repair genes, PTEN-PI3K, and other pathways drive the behavior of advanced prostate cancer allowing a better selection of therapies in each patient. Tumor testing for BRCA1 and BRCA2 is recommended for patients with metastatic prostate cancer, also considering a broad panel to guide decisions and genetic counseling. In symptomatic metastatic patients, castration should be stared to palliate symptoms and prolong survival. In high-risk or high-volume metastatic hormone-naïve patients, castration should be combined with docetaxel, abiraterone, enzalutamide or apalutamide. Radiotherapy to the primary tumor combined with systemic therapy is recommended in low-volume mHNPC patients. In patients with non-metastatic castration-resistant tumors, risk stratification can define the frequency of imaging. Adding enzalutamide, darolutamide or apalutamide to these patients prolongs metastasis-free and overall survival, but potential adverse events need to be taken into consideration. The choice of docetaxel, abiraterone or enzalutamide for treating metastatic castration-resistant patients depends on previous therapies, with cabazitaxel being also recommended after docetaxel. Olaparib is recommended in BRCA1/BRCA2 mutated castration-resistant patients after progression on at least one new hormonal therapy. Aggressive variants of prostate cancer respond to platinum-based chemotherapy. To optimize treatment efficiency, oncologists should incorporate all of these advances into an overall therapeutic strategy.


Subject(s)
Androgen Antagonists/therapeutic use , Antineoplastic Agents/therapeutic use , Prostatic Neoplasms/therapy , Androstenes/therapeutic use , Benzamides/therapeutic use , Combined Modality Therapy/methods , Docetaxel/therapeutic use , Genes, BRCA1 , Genes, BRCA2 , Genetic Testing/methods , Humans , Male , Medical Oncology , Nitriles/therapeutic use , Orchiectomy , Phenylthiohydantoin/therapeutic use , Phthalazines/therapeutic use , Piperazines/therapeutic use , Prostatic Neoplasms/genetics , Prostatic Neoplasms/pathology , Prostatic Neoplasms, Castration-Resistant/diagnosis , Prostatic Neoplasms, Castration-Resistant/therapy , Radiotherapy/methods , Randomized Controlled Trials as Topic , Societies, Medical , Spain , Thiohydantoins/therapeutic use
9.
Rev. esp. med. nucl. imagen mol. (Ed. impr.) ; 39(5): 327-336, sept.-oct. 2020. ilus, tab, graf
Article in Spanish | IBECS | ID: ibc-198297

ABSTRACT

La detección de nódulos pulmonares se ha incrementado en las últimas décadas debido a la introducción de los programas de cribado del cáncer de pulmón y al aumento de las exploraciones rutinarias de tomografía computarizada en los pacientes con neoplasias. La biopsia percutánea de estos nódulos no siempre permite caracterizarlos, por lo que en ocasiones es necesaria la biopsia quirúrgica, que a menudo requiere de localización prequirúrgica. La resección radioguiada de lesiones ocultas (ROLL) descrita para las lesiones mamarias se aplicó por primera vez en la resección de nódulos pulmonares en el año 2000, siendo en la actualidad una alternativa a otras técnicas de localización prequirúrgica como la resección guiada por arpón. La técnica aporta elevada tasa de detección con mínima morbimortalidad, potenciando el trabajo multidisciplinar entre los especialistas en Medicina Nuclear y los especialistas de radiodiagnóstico y cirugía torácica. En este trabajo, se describen las diferentes técnicas de localización prequirúrgica disponibles, los procesos metodológicos de la técnica ROLL y los resultados acumulados en 20 años de experiencia


The detection of pulmonary nodules has increased in recent decades due to the introduction of lung cancer screening programs and the massively use of routine chest computed tomography in patients with malignant neoplasms. Percutaneous biopsy of these nodules does not always characterize them, so sometimes a surgical biopsy is necessary, which often requires a presurgical localization. The radioguided occult lesion localization (ROLL) described for breast lesions was first applied in the resection of pulmonary nodules in 2000, becoming an alternative to other presurgical localization techniques such as hook-wire. The technique provides high detection rate with minimal morbidity, enhancing multidisciplinary work with specialists in Radiology and Chest Surgery. The present paper describes the different pre-surgical localization techniques currently available, the methodological procedure of the ROLL technique and the collected results in 20 years of experience


Subject(s)
Humans , Multiple Pulmonary Nodules/diagnostic imaging , Radiosurgery/methods , Solitary Pulmonary Nodule/diagnostic imaging , Lung Neoplasms/diagnostic imaging , Multiple Pulmonary Nodules/surgery , Radiotherapy, Image-Guided/methods , Solitary Pulmonary Nodule/surgery , Neoplasms, Unknown Primary/diagnostic imaging , Lung Neoplasms/surgery , Positron Emission Tomography Computed Tomography/methods
10.
Article in English, Spanish | MEDLINE | ID: mdl-32773359

ABSTRACT

The detection of pulmonary nodules has increased in recent decades due to the introduction of lung cancer screening programs and the massively use of routine chest computed tomography in patients with malignant neoplasms. Percutaneous biopsy of these nodules does not always characterize them, so sometimes a surgical biopsy is necessary, which often requires a presurgical localization. The radioguided occult lesion localization (ROLL) described for breast lesions was first applied in the resection of pulmonary nodules in 2000, becoming an alternative to other presurgical localization techniques such as hook-wire. The technique provides high detection rate with minimal morbidity, enhancing multidisciplinary work with specialists in Radiology and Chest Surgery. The present paper describes the different pre-surgical localization techniques currently available, the methodological procedure of the ROLL technique and the collected results in 20 years of experience.


Subject(s)
Multiple Pulmonary Nodules/diagnostic imaging , Positron Emission Tomography Computed Tomography/methods , Solitary Pulmonary Nodule/diagnostic imaging , Surgery, Computer-Assisted/methods , Early Detection of Cancer , Evidence-Based Medicine , Fiducial Markers , Humans , Intraoperative Period , Lung Neoplasms/diagnostic imaging , Lung Neoplasms/surgery , Multiple Pulmonary Nodules/surgery , Pneumonectomy , Positron-Emission Tomography , Punctures , Radionuclide Imaging , Radiopharmaceuticals , Solitary Pulmonary Nodule/surgery , Staining and Labeling/methods , Thoracic Surgery, Video-Assisted , Tomography, X-Ray Computed , Ultrasonography
11.
Ann Oncol ; 31(9): 1186-1197, 2020 09.
Article in English | MEDLINE | ID: mdl-32574722

ABSTRACT

BACKGROUND: A common polymorphism (1245A>C) in the HSD3B1 gene is associated with increased de novo synthesis of androgens and worse outcomes in men treated with androgen-deprivation therapy for metastatic castration-sensitive prostate cancer. The objective of the study was to determine whether this polymorphism is associated with outcomes for metastatic castration-resistant prostate cancer (mCRPC) treated with abiraterone or enzalutamide. PATIENTS AND METHODS: A total of 547 patients treated with abiraterone or enzalutamide from two prospective cohorts were evaluated. The HSD3B1 genotype was determined by targeted sequencing and/or TaqMan single-nucleotide polymorphism genotyping. In cohort 1, patients were randomized to receive abiraterone + prednisone or enzalutamide. In cohort 2, patients received either agent according to investigator's choice. Prostate-specific antigen (PSA) response rate, time to PSA progression (TTPP), time to progression (TTP) and overall survival were determined. Associations between HSD3B1 genotypes and outcomes were evaluated via univariate Cox regression. Multivariable Cox model was used to determine the independent association of each covariate. RESULTS: The HSD3B1 variant genotype (CC) was present in 15% of patients and was associated with worse TTP [hazard ratio (HR) 1.31, 95% confidence interval (CI) 1.02-1.67, P = 0.032] and PSA response rates (48% for CC versus 62% and 65% for AA and AC, respectively [P = 0.019]), with no significant difference in TTPP (HR 1.28, 95% CI 0.99-1.66, P = 0.064). The effect of genotype was similar for treatment with abiraterone or enzalutamide with a negative test for interaction for TTPP (P = 0.997) and TTP (P = 0.749). Multivariable analysis did not show a significant association between genotype and TTP or TTPP. CONCLUSIONS: The HSD3B1 (CC) genotype was associated with shorter TTP and lower PSA response rate in patients with mCRPC treated with abiraterone or enzalutamide. However, the CC genotype did not provide prognostic information beyond that conferred by standard clinical variables, suggesting that it may not be a suitable stand-alone biomarker in mCRPC.


Subject(s)
Androgen Antagonists , Phenylthiohydantoin , Prostatic Neoplasms, Castration-Resistant , Abiraterone Acetate , Androstenes , Benzamides , Germ Cells , Humans , Male , Multienzyme Complexes , Nitriles , Phenylthiohydantoin/analogs & derivatives , Prospective Studies , Prostate-Specific Antigen , Prostatic Neoplasms, Castration-Resistant/drug therapy , Prostatic Neoplasms, Castration-Resistant/genetics , Treatment Outcome
12.
Actas urol. esp ; 44(4): 245-250, mayo 2020. tab, graf
Article in Spanish | IBECS | ID: ibc-199008

ABSTRACT

INTRODUCCIÓN: Actualmente no existe ningún marcador pronóstico para el carcinoma renal de células claras (CRCC). La proteína STAT3 (Signal Transducer and Activator of Transcription 3) está implicada en la carcinogénesis del CRCC. Su activación se produce mediante fosforilación del residuo serina 727, translocándose al núcleo donde participa en la carcinogénesis y progresión tumoral. El objetivo primario del estudio fue evaluar la supervivencia cáncer-específica en una serie de 166 pacientes afectos de CRCC, y su posterior correlación con la expresión de pSer727-STAT3 como marcador pronóstico de CRCC. MATERIAL Y MÉTODOS: Realizamos un estudio retrospectivo en 166 pacientes con CRCC intervenidos mediante nefrectomía parcial o radical entre 2000 y 2010. Se construyó un microarray de tejido tumoral y se analizó la expresión inmunohistoquímica de pSer727-STAT3. La variable principal del estudio fue la supervivencia cáncer-específica. RESULTADOS: El grupo de riesgo según la UICC fue en 78 pacientes (47%) bajo, en 52 (31,3%) intermedio y en 36 (21,7%) alto; 11 pacientes (6,7%) debutaron con enfermedad metastásica. Durante un seguimiento medio de 97,2 meses (1-208), 37 pacientes (22,3%) desarrollaron recurrencia local y/o a distancia. La mortalidad cáncer-específica fue del 28,3% y la mortalidad global del 67,5%. La expresión media de pSer727-STAT3 fue de 92,9 (IC 95%:84,6-101,1) sin observarse relación con grupos de riesgo u otros factores pronósticos. En un análisis de regresión logística de Cox, pSer727-STAT3 no se comportó como un predictor independiente de mortalidad cáncer-específica. Sin embargo, en pacientes de alto riesgo y metastásicos, la supervivencia cáncer-específica fue significativamente mayor cuando la expresión de pSer727-STAT3 fue inferior a 110, HR: 5,4 (IC 96%:1,8-16,4) y HR: 2,3 (IC 95%: 1,1-4,6) respectivamente, p > 0,001. CONCLUSIONES: pSer727-STAT3 no es un marcador de supervivencia en los pacientes con CRCC. Sin embargo, en pacientes de alto riesgo, es un marcador de supervivencia cáncer-específica, incluso en pacientes metastásicos que reciben tratamiento con antiangiogénicos


INTRODUCTION: Currently, clear cell renal carcinoma (CCRCC) has no prognostic markers. STAT3 protein (Signal Transducer and Activator of Transcription 3) is involved in the carcinogenesis of CCRCC. Its activation is produced by phosphorylation of the serine 727 residue, translocating to the nucleus where it is involved in carcinogenesis and tumor progression. The primary objective of the study was to evaluate cancer-specific survival rates in a series of 166 patients with CCRCC, and its subsequent correlation with the expression of pSer727-STAT3 as a prognostic marker of CCRCC. MATERIAL AND METHODS: We conducted a retrospective study on 166 patients with CCRCC undergoing partial or radical nephrectomy between 2000 and 2010. A tumor tissue microarray was constructed for immunohistochemical analysis of pSer727-STAT3 expression. The main variable of the study was cancer-specific survival. RESULTS: Patients were classified according to the UICC risk groups as follows: low in 78 patients (47%), intermediate in 52 (31.3%) and high 36 (21.7%); 11 patients (6.7%) were diagnosed with metastatic disease. During a mean follow-up of 97.2 months (1-208), 37 patients (22.3%) developed local and/or distant recurrence. Cancer-specific and overall mortality rates were 28.3% and 67.5%, respectively. The mean expression of pSer727-STAT3 was 92.9 (95% CI: 84.6-101.1) without showing any relationship with risk groups or other prognostic factors. In a Cox logistic regression analysis, pSer727-STAT3 did not behave as an independent predictor of cancer-specific mortality. However, in high-risk and metastatic patients, cancer-specific survival was significantly higher when the expression of pSer727-STAT3 was lower than 110, HR: 5.4 (96% CI: 1.8-16.4) and HR: 2.3 (95% CI: 1.1-4.6) respectively, P<.001. CONCLUSIONS: pSer727-STAT3 is not a survival marker in patients with CCRCC. However, it is a cancer-specific survival marker in high-risk patients, even in metastatic patients undergoing treatment with antiangiogenic agents


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Aged , Aged, 80 and over , Biomarkers, Tumor/physiology , Carcinoma, Renal Cell/diagnosis , Kidney Neoplasms/diagnosis , STAT3 Transcription Factor/physiology , Prognosis , Retrospective Studies , Survival Analysis , Neoplasm Metastasis , Carcinoma, Renal Cell/mortality , Kidney Neoplasms/mortality
13.
Actas Urol Esp (Engl Ed) ; 44(4): 245-250, 2020 May.
Article in English, Spanish | MEDLINE | ID: mdl-32247519

ABSTRACT

INTRODUCTION: Currently, clear cell renal carcinoma (CCRCC) has no prognostic markers. STAT3 protein (Signal Transducer and Activator of Transcription 3) is involved in the carcinogenesis of CCRCC. Its activation is produced by phosphorylation of the serine 727 residue, translocating to the nucleus where it is involved in carcinogenesis and tumor progression. The primary objective of the study was to evaluate cancer-specific survival rates in a series of 166 patients with CCRCC, and its subsequent correlation with the expression of pSer727-STAT3 as a prognostic marker of CCRCC. MATERIAL AND METHODS: We conducted a retrospective study on 166 patients with CCRCC undergoing partial or radical nephrectomy between 2000 and 2010. A tumor tissue microarray was constructed for immunohistochemical analysis of pSer727-STAT3 expression. The main variable of the study was cancer-specific survival. RESULTS: Patients were classified according to the UICC risk groups as follows: low in 78 patients (47%), intermediate in 52 (31.3%) and high 36 (21.7%); 11 patients (6.7%) were diagnosed with metastatic disease. During a mean follow-up of 97.2 months (1-208), 37 patients (22.3%) developed local and/or distant recurrence. Cancer-specific and overall mortality rates were 28.3% and 67.5%, respectively. The mean expression of pSer727-STAT3 was 92.9 (95% CI: 84.6-101.1) without showing any relationship with risk groups or other prognostic factors. In a Cox logistic regression analysis, pSer727-STAT3 did not behave as an independent predictor of cancer-specific mortality. However, in high-risk and metastatic patients, cancer-specific survival was significantly higher when the expression of pSer727-STAT3 was lower than 110, HR: 5.4 (96% CI: 1.8-16.4) and HR: 2.3 (95% CI: 1.1-4.6) respectively, P<.001. CONCLUSIONS: pSer727-STAT3 is not a survival marker in patients with CCRCC. However, it is a cancer-specific survival marker in high-risk patients, even in metastatic patients undergoing treatment with antiangiogenic agents.


Subject(s)
Carcinoma, Renal Cell/metabolism , Carcinoma, Renal Cell/mortality , Carcinoma, Renal Cell/surgery , Kidney Neoplasms/metabolism , Kidney Neoplasms/mortality , STAT3 Transcription Factor/biosynthesis , Aged , Female , Humans , Kidney Neoplasms/surgery , Male , Middle Aged , Nephrectomy/methods , Prognosis , Retrospective Studies , Survival Rate
14.
Clin Transl Oncol ; 22(11): 2126-2129, 2020 Nov.
Article in English | MEDLINE | ID: mdl-32198642

ABSTRACT

In castration-resistant prostate cancer (CRPC) patients, observational studies have reported that statins may boost the antitumor activity of abiraterone (AA) and data suggest an improvement in efficacy; conclusions with vitamin D are less clear but an eventual benefit has been pointed. We conducted a post hoc analysis of individual patient data of CRPC patients treated with prednisone and/or AA with or without statins/vitamin D on randomized clinical trials. In the COU-AA-301 trial, use of AA with statin and vitamin D reduced the risk of death by 38% (p = 0.0007) while AA alone was associated with a decrease of 10% (p = 0.025), compared to prednisone alone. Meanwhile, in the COU-AA-302 trial, use of AA plus statin plus vitamin D was associated with a reduced risk of death of 26% (p = 0.0054). In this data analysis from two prospective randomized clinical trials, statin and vitamin D use was associated with superior overall survival in metastatic CRPC patients treated with AA and prednisone. To our knowledge, this is the first report suggesting the impact of statin plus vitamin D in this population. New strategies using big data may help to clarify these questions easily and in a most cost-effective approach.


Subject(s)
Hydroxymethylglutaryl-CoA Reductase Inhibitors/administration & dosage , Prostatic Neoplasms, Castration-Resistant/drug therapy , Vitamin D/administration & dosage , Androstenes/therapeutic use , Drug Therapy, Combination , Humans , Male , Neoplasm Metastasis , Prednisone/therapeutic use , Prospective Studies , Prostatic Neoplasms, Castration-Resistant/mortality , Prostatic Neoplasms, Castration-Resistant/pathology , Randomized Controlled Trials as Topic
17.
Phys Rev Lett ; 122(16): 165701, 2019 Apr 26.
Article in English | MEDLINE | ID: mdl-31075017

ABSTRACT

Positron annihilation lifetime spectroscopy is used to experimentally demonstrate the direct relationship between vacancies and the shift of the martensitic transformation temperature in a Ni_{55}Fe_{17}Ga_{28} alloy. The evolution of vacancies assisting the ordering enables shifts of the martensitic transformation up to 50 K. Our results confirm the role that both vacancy concentration and different vacancy dynamics play in samples quenched from the L2_{1} and B2 phases, which dictate the martensitic transformation temperature and its subsequent evolution. Finally, by electron-positron density functional calculations V_{Ni} is identified as the most probable vacancy present in Ni_{55}Fe_{17}Ga_{28}. This work evidences the capability of vacancies for the fine-tuning of the martensitic transformation temperature, paving the way for defect engineering of multifunctional properties.

18.
Actas urol. esp ; 43(3): 118-123, abr. 2019. graf
Article in Spanish | IBECS | ID: ibc-181169

ABSTRACT

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


Subject(s)
Kidney Neoplasms/etiology , Carcinoma, Renal Cell/diagnosis , STAT3 Transcription Factor/metabolism , Biomarkers, Tumor , Carcinoma, Renal Cell/physiopathology , Prognosis , Carcinoma, Renal Cell/etiology , STAT3 Transcription Factor/therapeutic use
19.
Actas urol. esp ; 43(3): 137-142, abr. 2019. ilus, graf, tab
Article in Spanish | IBECS | ID: ibc-181172

ABSTRACT

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


Subject(s)
Humans , Male , Aged , Middle Aged , Prostatectomy/methods , Robotic Surgical Procedures/methods , Urinary Incontinence/diagnosis , Magnetic Resonance Spectroscopy/instrumentation , Prognosis , Preoperative Period , Recovery of Function/physiology , Prospective Studies , Prostate/pathology , Prostatic Neoplasms
20.
Actas Urol Esp (Engl Ed) ; 43(3): 137-142, 2019 Apr.
Article in English, Spanish | MEDLINE | ID: mdl-30420112

ABSTRACT

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.


Subject(s)
Magnetic Resonance Imaging , Prostatectomy/methods , Robotic Surgical Procedures , Urethra/diagnostic imaging , Urinary Incontinence/epidemiology , Aged , Humans , Male , Middle Aged , Predictive Value of Tests , Preoperative Period , Prospective Studies , Recovery of Function , Urethra/anatomy & histology , Urination
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