TY - JOUR
T1 - Use of radiotherapy in patients with oesophageal, stomach, colon, rectal, liver, pancreatic, lung, and ovarian cancer: an International Cancer Benchmarking Partnership (ICBP) population-based study
AU - McPhail, Sean
AU - Barclay, Matthew E.
AU - Swann, Ruth
AU - Johnson, Shane A.
AU - Alvi, Riaz
AU - Barisic, Andriana
AU - Bucher, Oliver
AU - Creighton, Nicola
AU - Denny, C.A.
AU - Dewar, R.A.
AU - Donnelly, D.W.
AU - Dowden, Jeff J.
AU - Downie, Laura
AU - Finn, Nora
AU - Gavin, Anna T.
AU - Habbous, Steven
AU - Huws, Dyfed W.
AU - Kumar, S. Eshwar
AU - May, Leon
AU - McClure, Carol A.
AU - Morrison, David S.
AU - Møller, Bjorn
AU - Musto, Grace
AU - Nilssen, Yngvar
AU - Saint-Jacques, Nathalie
AU - Sarker, Sabuj
AU - Shack, Lorraine
AU - Tian, Xiaoyi
AU - Thomas, Robert J. S.
AU - Wang, Haiyan
AU - Woods, Ryan R.
AU - You, Hui
AU - Zhang, Bin
AU - Lyratzopoulos, Georgios
AU - Bennett, D.
AU - Butler, J.
AU - Cameron, D.A.
AU - Chew, C.
AU - Crosby, T.
AU - Filsinger, B.
AU - Finley, C.J.
AU - Forster, K.
AU - Fung, S.
AU - Green, B.
AU - Gomez-Navas, E.
AU - Gutierrez, E.
AU - Han, J.
AU - Harrison, S.
AU - Lawler, M.
AU - Little, A.L.
AU - Pantarotto, J.R.
AU - Peacock, S.J.
AU - Ray-Coquard, I.
AU - Thomson, C.S.
AU - Warlow, J.L.
AU - Whitfield, E.
PY - 2024/3/1
Y1 - 2024/3/1
N2 - Background There is little evidence on variation in radiotherapy use in different countries, although it is a keytreatment modality for some patients with cancer. Here we aimed to examine such variation.Methods This population-based study used data from Norway, the four UK nations (England, Northern Ireland,Scotland, and Wales), nine Canadian provinces (Alberta, British Columbia, Manitoba, New Brunswick, Newfoundlandand Labrador, Nova Scotia, Ontario, Prince Edward Island, and Saskatchewan), and two Australian states(New South Wales and Victoria). Patients aged 15–99 years diagnosed with cancer in eight different sites (oesophageal,stomach, colon, rectal, liver, pancreatic, lung, or ovarian cancer), with no other primary cancer diagnosis occurringwithin the 5 years before to 1 year after the index cancer diagnosis or during the study period were included in thestudy. We examined variation in radiotherapy use from 31 days before to 365 days after diagnosis and time to itsinitiation, alongside related variation in patient group differences. Information was obtained from cancer registryrecords linked to clinical or patient management system data, or hospital administration data. Random-effects metaanalyses quantified interjurisdictional variation using 95% prediction intervals (95% PIs).Findings Between Jan 1, 2012, and Dec 31, 2017, of 902 312 patients with a new diagnosis of one of the studiedcancers, 115 357 (12·8%) did not meet inclusion criteria, and 786,955 were included in the analysis. There was largeinterjurisdictional variation in radiotherapy use, with wide 95% PIs: 17·8 to 82·4 (pooled estimate 50·2%) foroesophageal cancer, 35·5 to 55·2 (45·2%) for rectal cancer, 28·6 to 54·0 (40·6%) for lung cancer, and4·6 to 53·6 (19·0%) for stomach cancer. For patients with stage 2–3 rectal cancer, interjurisdictional variation wasgreater than that for all patients with rectal cancer (95% PI 37·0 to 84·6; pooled estimate 64·2%). Radiotherapy usewas infrequent but variable in patients with pancreatic (95% PI 1·7 to 16·5%), liver (1·8 to 11·2%), colon (1·6 to 5·0%),and ovarian (0·8 to 7·6%) cancer. Patients aged 85–99 years had three-times lower odds of radiotherapy use thanthose aged 65–74 years, with substantial interjurisdictional variation in this age difference (odds ratio [OR] 0·38;95% PI 0·20–0·73). Women had slightly lower odds of radiotherapy use than men (OR 0·88, 95% PI 0·77–1·01).There was large variation in median time to first radiotherapy (from diagnosis date) by cancer site, with substantialinterjurisdictional variation (eg, oesophageal 95% PI 11·3 days to 112·8 days; pooled estimate 62·0 days; rectal95% PI 34·7 days to 77·3 days; pooled estimate 56·0 days). Older patients had shorter median time to radiotherapywith appreciable interjurisdictional variation (−9·5 days in patients aged 85–99 years vs 65–74 years, 95% PI−26·4 to 7·4).Interpretation Large interjurisdictional variation in both use and time to radiotherapy initiation were observed,alongside large and variable age differences. To guide efforts to improve patient outcomes, underlying reasons forthese differences need to be established.
AB - Background There is little evidence on variation in radiotherapy use in different countries, although it is a keytreatment modality for some patients with cancer. Here we aimed to examine such variation.Methods This population-based study used data from Norway, the four UK nations (England, Northern Ireland,Scotland, and Wales), nine Canadian provinces (Alberta, British Columbia, Manitoba, New Brunswick, Newfoundlandand Labrador, Nova Scotia, Ontario, Prince Edward Island, and Saskatchewan), and two Australian states(New South Wales and Victoria). Patients aged 15–99 years diagnosed with cancer in eight different sites (oesophageal,stomach, colon, rectal, liver, pancreatic, lung, or ovarian cancer), with no other primary cancer diagnosis occurringwithin the 5 years before to 1 year after the index cancer diagnosis or during the study period were included in thestudy. We examined variation in radiotherapy use from 31 days before to 365 days after diagnosis and time to itsinitiation, alongside related variation in patient group differences. Information was obtained from cancer registryrecords linked to clinical or patient management system data, or hospital administration data. Random-effects metaanalyses quantified interjurisdictional variation using 95% prediction intervals (95% PIs).Findings Between Jan 1, 2012, and Dec 31, 2017, of 902 312 patients with a new diagnosis of one of the studiedcancers, 115 357 (12·8%) did not meet inclusion criteria, and 786,955 were included in the analysis. There was largeinterjurisdictional variation in radiotherapy use, with wide 95% PIs: 17·8 to 82·4 (pooled estimate 50·2%) foroesophageal cancer, 35·5 to 55·2 (45·2%) for rectal cancer, 28·6 to 54·0 (40·6%) for lung cancer, and4·6 to 53·6 (19·0%) for stomach cancer. For patients with stage 2–3 rectal cancer, interjurisdictional variation wasgreater than that for all patients with rectal cancer (95% PI 37·0 to 84·6; pooled estimate 64·2%). Radiotherapy usewas infrequent but variable in patients with pancreatic (95% PI 1·7 to 16·5%), liver (1·8 to 11·2%), colon (1·6 to 5·0%),and ovarian (0·8 to 7·6%) cancer. Patients aged 85–99 years had three-times lower odds of radiotherapy use thanthose aged 65–74 years, with substantial interjurisdictional variation in this age difference (odds ratio [OR] 0·38;95% PI 0·20–0·73). Women had slightly lower odds of radiotherapy use than men (OR 0·88, 95% PI 0·77–1·01).There was large variation in median time to first radiotherapy (from diagnosis date) by cancer site, with substantialinterjurisdictional variation (eg, oesophageal 95% PI 11·3 days to 112·8 days; pooled estimate 62·0 days; rectal95% PI 34·7 days to 77·3 days; pooled estimate 56·0 days). Older patients had shorter median time to radiotherapywith appreciable interjurisdictional variation (−9·5 days in patients aged 85–99 years vs 65–74 years, 95% PI−26·4 to 7·4).Interpretation Large interjurisdictional variation in both use and time to radiotherapy initiation were observed,alongside large and variable age differences. To guide efforts to improve patient outcomes, underlying reasons forthese differences need to be established.
U2 - 10.1016/S1470-2045(24)00032-9
DO - 10.1016/S1470-2045(24)00032-9
M3 - Article
SN - 1470-2045
VL - 25
SP - 352
EP - 365
JO - The Lancet Oncology
JF - The Lancet Oncology
ER -