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2.
J Gastrointest Surg ; 22(6): 1007-1015, 2018 06.
Artículo en Inglés | MEDLINE | ID: mdl-29435899

RESUMEN

INTRODUCTION: Conflicting evidence exists from randomized controlled trials supporting both increased complications/fistulae and improved outcomes with drain placement after pancreatectomy. The objective was to determine drain practice patterns in the USA, and to identify if drain placement was associated with fistula formation. METHODS: Demographic, perioperative, and patient outcome data were captured from the most recent annual NSQIP pancreatic demonstration project database, including components of the fistula risk score. Significant variables in univariate analysis were entered into adjusted logistic regression models. RESULTS: Of 5013 pancreatectomy patients, 4343 (87%) underwent drain placement and 18% of patients experienced a pancreatic fistula. When controlled for other factors, drain placement was associated with ducts < 3 mm, soft glands, and blood transfusion within 72 h of surgery. Age, obesity, neoadjuvant radiation, preoperative INR level, and malignant histology lost significance in the adjusted model. Drained patients experienced higher readmission rates (17 vs. 14%; p < 0.05) and increased (20 vs. 8%; p < 0.01) pancreatic fistulae. Fistula was associated with obesity, no neoadjuvant chemotherapy, drain placement, < 3 mm duct diameter, soft gland, and longer operative times. Drain placement remained independently associated with fistula after both distal pancreatectomy (OR = 2.84 (1.70, 4.75); p < 0.01) and pancreatoduodenectomy (OR = 2.29 (1.28, 4.11); p < 0.01). CONCLUSIONS: Despite randomized controlled clinical trial data supporting no drain placement, drains are currently placed in the vast majority (87%) of pancreatectomy patients from > 100 institutions in the USA, particularly those with soft glands, small ducts, and perioperative blood transfusions. When these factors are controlled for, drain placement remains independently associated with fistulae after both distal and proximal pancreatectomy.


Asunto(s)
Drenaje/estadística & datos numéricos , Pancreatectomía/efectos adversos , Conductos Pancreáticos/patología , Fístula Pancreática/epidemiología , Pancreaticoduodenectomía/efectos adversos , Anciano , Drenaje/efectos adversos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Obesidad/epidemiología , Tempo Operativo , Tamaño de los Órganos , Fístula Pancreática/etiología , Readmisión del Paciente/estadística & datos numéricos , Factores de Riesgo
4.
Cancer Gene Ther ; 24(3): 134-140, 2017 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-27834354

RESUMEN

Recent clinical successes with immunotherapy have resulted in expanding indications for cancer therapy. To enhance antitumor immune responses, and to better choose specific strategies matched to patient and tumor characteristics, genomic-driven precision immunotherapy will be necessary. Herein, we explore the role that tumor gene-expression profiling (GEP) may have in the prediction of an immunotherapeutic response. Genetic markers associated with response to immunotherapy are addressed as they pertain to the tumor genomic landscape, the extent of DNA damage, tumor mutational load and tumor-specific neoantigens. Furthermore, genetic markers associated with resistance to checkpoint blockade and relapse are reviewed. Finally, the utility of GEP to identify new tumor types for immunotherapy and implications for combinatorial strategies are summarized.


Asunto(s)
Biomarcadores de Tumor , Perfilación de la Expresión Génica , Regulación Neoplásica de la Expresión Génica , Inmunoterapia , Neoplasias/genética , Neoplasias/terapia , Animales , Antígenos de Neoplasias/inmunología , Terapia Combinada , Daño del ADN , Resistencia a Antineoplásicos/genética , Marcadores Genéticos , Genómica/métodos , Humanos , Inmunoterapia/métodos , Terapia Molecular Dirigida , Mutación , Neoplasias/inmunología , Neoplasias/patología , Pronóstico , Recurrencia , Transcriptoma , Resultado del Tratamiento
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