2019
DOI: 10.1093/ije/dyz076
|View full text |Cite
|
Sign up to set email alerts
|

Data Resource Profile: National Cancer Registration Dataset in England

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
164
0

Year Published

2019
2019
2023
2023

Publication Types

Select...
9

Relationship

2
7

Authors

Journals

citations
Cited by 174 publications
(165 citation statements)
references
References 18 publications
1
164
0
Order By: Relevance
“…The NCDA represents a unique combination of information provided by GPs and other health-care professionals based on clinical insight and judgment, with high-quality information about patient and tumour characteristics from the national cancer registry in England. 17,25 Presenting symptoms of patients with cancer In addition to adjusting our findings by sociodemographic factors, we adjusted our results by cancer site. Although this adjustment did not appear to substantially alter the observed patterns of variation, the associations between symptoms and stage at diagnosis might differ in a population-based incident cohort with a different distribution of cancer sites.…”
Section: Discussionmentioning
confidence: 99%
“…The NCDA represents a unique combination of information provided by GPs and other health-care professionals based on clinical insight and judgment, with high-quality information about patient and tumour characteristics from the national cancer registry in England. 17,25 Presenting symptoms of patients with cancer In addition to adjusting our findings by sociodemographic factors, we adjusted our results by cancer site. Although this adjustment did not appear to substantially alter the observed patterns of variation, the associations between symptoms and stage at diagnosis might differ in a population-based incident cohort with a different distribution of cancer sites.…”
Section: Discussionmentioning
confidence: 99%
“…NCRAS collects data on all cancers diagnosed in England. This includes demographic information, date of diagnosis, treatment and vital status through the Office for National Statistics 22. The survey, however, includes only patients discharged in a recent 3-month period from hospital, regardless of their date of diagnosis.…”
Section: Methodsmentioning
confidence: 99%
“…The National Cancer Registration and Analysis Service (NCRAS) collects data on all incident cancer diagnoses in England 22. Focusing on the four most common cancers in England (colorectal, lung, breast and prostate), we aimed to compare the survey responders’ demographic and tumour stage at diagnosis and their median survival time to determine the extent to which they represent the cancer registry population and to inform future surveys.…”
Section: Introductionmentioning
confidence: 99%
“…A cohort of 27 719 primary diagnoses of endometrial cancer (identified using International Classification of Diseases 10th revision codes as C54, including carcinoma, adenocarcinoma, adenosquamous, serous, clear cell histological types only [see Supplementary material, Table S1]) in England between 2013 and 2016 was obtained from Public Health England's national cancer registry data . This was linked to SACT (Systemic Anti‐Cancer Therapy), RTDS (Radiotherapy DataSet) and inpatient HES (Hospital Episode Statistics) data sets to obtain additional chemotherapy, radiotherapy and surgery data, respectively.…”
Section: Methodsmentioning
confidence: 99%