Cazzaniga Walter, Ventimiglia Eugenio, Alfano Massimo, Robinson David, Lissbrant Ingela Franck, Carlsson Stefan, Styrke Johan, Montorsi Francesco, Salonia Andrea, Stattin Pär
Division of Experimental Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.
University Vita-Salute San Raffaele, Milan, Italy.
Front Med (Lausanne). 2019 Mar 22;6:51. doi: 10.3389/fmed.2019.00051. eCollection 2019.
Given the increasing prevalence of cancer, it is vital to systematically collect data in order to monitor disease trends and quality of cancer care. For this purpose, clinical cancer registries have been developed in some countries. These registers are intended to be used as a basis for quality assurance and quality improvement, but they also constitute a rich resource of real world data for research. The aim of this mini-review was to describe the structure and the organization of the National Prostate Cancer Register (NPCR) with some examples on how data in NPCR have affected prostate cancer care in Sweden.
鉴于癌症的患病率不断上升,系统地收集数据以监测疾病趋势和癌症护理质量至关重要。为此,一些国家已建立了临床癌症登记处。这些登记处旨在用作质量保证和质量改进的基础,但它们也构成了用于研究的丰富的真实世界数据资源。本小型综述的目的是描述国家前列腺癌登记处(NPCR)的结构和组织,并举例说明NPCR中的数据如何影响瑞典的前列腺癌护理。