2010
DOI: 10.1111/j.1464-410x.2009.08834.x
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Initial management of prostate cancer: first year experience with the Norwegian National Prostate Cancer Registry

Abstract: Study Type – Therapy (individual cohort)
 Level of Evidence 2b OBJECTIVE Improving a country’s management of cancer patients requires continuous evaluation, and requires the availability of population‐based prognostic and therapeutic variables. We aimed to document the national diagnostic and therapeutic tasks in Norwegian patients with prostate cancer diagnosed in 2004, with the 2003 European Association of Urology (EAU) guidelines representing the background. PATIENTS AND METHODS The Norwegian Prostate Cance… Show more

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Cited by 39 publications
(39 citation statements)
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“…National diagnostic and therapeutic interventions available to Norwegian patients with PCa in the context of EAU guidelines [127] Treatment and 5-yr survival in patients with nonmetastatic PCa [128] J-CaP: Japanese Study Group of Prostate Cancer…”
Section: Caesar: Comparative Effectivenessmentioning
confidence: 99%
“…National diagnostic and therapeutic interventions available to Norwegian patients with PCa in the context of EAU guidelines [127] Treatment and 5-yr survival in patients with nonmetastatic PCa [128] J-CaP: Japanese Study Group of Prostate Cancer…”
Section: Caesar: Comparative Effectivenessmentioning
confidence: 99%
“…PCa-related variables and operative modality were retrieved from the medical records and the National Prostate Cancer Registry [ 6 ] . Risk groups were defi ned according to D ' Amico et al .…”
Section: Cancer-and Treatment-related Variablesmentioning
confidence: 99%
“…15 In October 2006, patients still alive (n ¼ 2998) were invited to participate in a cross-sectional postal survey with 2194 respondents (compliance rate 73%). For the present study, a subgroup was selected (n ¼ 531) containing survivors for whom X12 months had elapsed since the start of curative treatment and who never had undergone orchiectomy or ADT prior to the survey, according to patients' selfreport and data from NorPD.…”
Section: Study Populationmentioning
confidence: 99%
“…CF was defined as a sum score of X4 after dichotomization of the Fatigue Questionnaire symptom scores and duration for X6 months. 17 Table 1 summarizes other variables of interest for our analyses and their definition: age at diagnosis, observation time (months from treatment start to survey and divided in three subintervals comprising comparable numbers of patients), D'Amico risk group 15,18 based on T-category, Gleason score and PSA, Eastern Cooperative Oncology Group-status 19 and medication for chronic diseases reflecting pretreatment co-morbidity (0, no medication for chronic disease; 1, medication for one chronic disease; 2, medication for two or more chronic diseases).…”
Section: Cf and Variables In Studymentioning
confidence: 99%