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2015
DOI: 10.1111/codi.13060
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Time trends, improvements and national auditing of rectal cancer management over an 18‐year period

Abstract: There have been substantial changes over time in the management of patients with rectal cancer, reflected in improved outcome. Much indirect evidence indicates that auditing matters, but without a control group it is not possible to draw firm conclusions regarding the possible impact of a quality control registry on faster shifts in time trends, decreased variability and improvements. Registry data were made available for reference.

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Cited by 85 publications
(69 citation statements)
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References 36 publications
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“…These changes include centralized and improved surgery, multidisciplinary teams [3][4][5], preoperative radiotherapy in rectal cancer [9,10] and more precise adjuvant treatments [6][7][8]. However, also the regional healthcare systems have changed accordingly, and based on a single clinical trial or study registry, it is challenging to analyze the impact of different changes in the treatment results of CRC.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…These changes include centralized and improved surgery, multidisciplinary teams [3][4][5], preoperative radiotherapy in rectal cancer [9,10] and more precise adjuvant treatments [6][7][8]. However, also the regional healthcare systems have changed accordingly, and based on a single clinical trial or study registry, it is challenging to analyze the impact of different changes in the treatment results of CRC.…”
Section: Discussionmentioning
confidence: 99%
“…Controlled quality and centralization of surgery, both in rectal [3,4] and colon cancer [5] and the use of adjuvant chemotherapy [6][7][8] have improved the survival of patients with CRC. Additionally, in rectal cancer, preoperative radiotherapy or chemoradiotherapy have significantly improved survival [9,10].…”
Section: Introductionmentioning
confidence: 99%
“…The SCRCR is a national population-based registry that prospectively collects data for all patients with colorectal cancer. This registry has previously been described in detail [16, 20, 22]. Primary data—information about patients (age and gender), tumours (TNM stage), preoperative assessment, neoadjuvant treatment, surgical treatment, residual tumour status, and early complications—are reported 30 days after surgery or at diagnosis for patients not treated with surgery.…”
Section: Methodsmentioning
confidence: 99%
“…During the early years, most patients received 25 Gy/5d and immediate surgery, and only a few patients with locally advanced tumours received 50 Gy/25d, often combined with chemotherapy and delayed surgery. In 2013, approximately 80% of the patients who received neoadjuvant therapy had a short-course RT and the remaining had chemoradiotherapy [19, 22]. There were no standardised national follow-up guidelines during the period studied, but the patients were followed according to each hospital’s protocols.…”
Section: Methodsmentioning
confidence: 99%
“…Patients diagnosed with rectal cancer in stage I-III 18-61 years of age 1996-2009, and treated curatively (n ¼ 3438) were identified in the Swedish Colorectal Cancer Register. The register contains comprehensive clinical information and covers >98% of all national invasive rectal adenocarcinomas (20,21).…”
Section: Study Populationmentioning
confidence: 99%