| Literature DB >> 28095147 |
Antonio Finelli1, Nofisat Ismaila1, Bill Bro1, Jeremy Durack1, Scott Eggener1, Andrew Evans1, Inderbir Gill1, David Graham1, William Huang1, Michael A S Jewett1, Sheron Latcha1, William Lowrance1, Mitchell Rosner1, Bobby Shayegan1, R Houston Thompson1, Robert Uzzo1, Paul Russo1.
Abstract
Purpose To provide recommendations for the management options for patients with small renal masses (SRMs). Methods By using a literature search and prospectively defined study selection, we sought systematic reviews, meta-analyses, randomized clinical trials, prospective comparative observational studies, and retrospective studies published from 2000 through 2015. Outcomes included recurrence-free survival, disease-specific survival, and overall survival. Results Eighty-three studies, including 20 systematic reviews and 63 primary studies, met the eligibility criteria and form the evidentiary basis for the guideline recommendations. Recommendations On the basis of tumor-specific findings and competing risks of mortality, all patients with an SRM should be considered for a biopsy when the results may alter management. Active surveillance should be an initial management option for patients who have significant comorbidities and limited life expectancy. Partial nephrectomy (PN) for SRMs is the standard treatment that should be offered to all patients for whom an intervention is indicated and who possess a tumor that is amenable to this approach. Percutaneous thermal ablation should be considered an option if complete ablation can reliably be achieved. Radical nephrectomy for SRMs should only be reserved for patients who possess a tumor of significant complexity that is not amenable to PN or for whom PN may result in unacceptable morbidity even when performed at centers with expertise. Referral to a nephrologist should be considered if chronic kidney disease (estimated glomerular filtration rate < 45 mL/min/1.73 m2) or progressive chronic kidney disease occurs after treatment, especially if associated with proteinuria.Entities:
Mesh:
Year: 2017 PMID: 28095147 DOI: 10.1200/JCO.2016.69.9645
Source DB: PubMed Journal: J Clin Oncol ISSN: 0732-183X Impact factor: 44.544