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Mortality due to cancer treatment delay: systematic review and meta-analysis

OBJECTIVE: To quantify the association of cancer treatment delay and mortality for each four week increase in delay to inform cancer treatment pathways. DESIGN: Systematic review and meta-analysis. DATA SOURCES: Published studies in Medline from 1 January 2000 to 10 April 2020. ELIGIBILITY CRITERIA...

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Autores principales: Hanna, Timothy P, King, Will D, Thibodeau, Stephane, Jalink, Matthew, Paulin, Gregory A, Harvey-Jones, Elizabeth, O’Sullivan, Dylan E, Booth, Christopher M, Sullivan, Richard, Aggarwal, Ajay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7610021/
https://www.ncbi.nlm.nih.gov/pubmed/33148535
http://dx.doi.org/10.1136/bmj.m4087
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author Hanna, Timothy P
King, Will D
Thibodeau, Stephane
Jalink, Matthew
Paulin, Gregory A
Harvey-Jones, Elizabeth
O’Sullivan, Dylan E
Booth, Christopher M
Sullivan, Richard
Aggarwal, Ajay
author_facet Hanna, Timothy P
King, Will D
Thibodeau, Stephane
Jalink, Matthew
Paulin, Gregory A
Harvey-Jones, Elizabeth
O’Sullivan, Dylan E
Booth, Christopher M
Sullivan, Richard
Aggarwal, Ajay
author_sort Hanna, Timothy P
collection PubMed
description OBJECTIVE: To quantify the association of cancer treatment delay and mortality for each four week increase in delay to inform cancer treatment pathways. DESIGN: Systematic review and meta-analysis. DATA SOURCES: Published studies in Medline from 1 January 2000 to 10 April 2020. ELIGIBILITY CRITERIA FOR SELECTING STUDIES: Curative, neoadjuvant, and adjuvant indications for surgery, systemic treatment, or radiotherapy for cancers of the bladder, breast, colon, rectum, lung, cervix, and head and neck were included. The main outcome measure was the hazard ratio for overall survival for each four week delay for each indication. Delay was measured from diagnosis to first treatment, or from the completion of one treatment to the start of the next. The primary analysis only included high validity studies controlling for major prognostic factors. Hazard ratios were assumed to be log linear in relation to overall survival and were converted to an effect for each four week delay. Pooled effects were estimated using DerSimonian and Laird random effect models. RESULTS: The review included 34 studies for 17 indications (n=1 272 681 patients). No high validity data were found for five of the radiotherapy indications or for cervical cancer surgery. The association between delay and increased mortality was significant (P<0.05) for 13 of 17 indications. Surgery findings were consistent, with a mortality risk for each four week delay of 1.06-1.08 (eg, colectomy 1.06, 95% confidence interval 1.01 to 1.12; breast surgery 1.08, 1.03 to 1.13). Estimates for systemic treatment varied (hazard ratio range 1.01-1.28). Radiotherapy estimates were for radical radiotherapy for head and neck cancer (hazard ratio 1.09, 95% confidence interval 1.05 to 1.14), adjuvant radiotherapy after breast conserving surgery (0.98, 0.88 to 1.09), and cervix cancer adjuvant radiotherapy (1.23, 1.00 to 1.50). A sensitivity analysis of studies that had been excluded because of lack of information on comorbidities or functional status did not change the findings. CONCLUSIONS: Cancer treatment delay is a problem in health systems worldwide. The impact of delay on mortality can now be quantified for prioritisation and modelling. Even a four week delay of cancer treatment is associated with increased mortality across surgical, systemic treatment, and radiotherapy indications for seven cancers. Policies focused on minimising system level delays to cancer treatment initiation could improve population level survival outcomes.
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spelling pubmed-76100212020-11-05 Mortality due to cancer treatment delay: systematic review and meta-analysis Hanna, Timothy P King, Will D Thibodeau, Stephane Jalink, Matthew Paulin, Gregory A Harvey-Jones, Elizabeth O’Sullivan, Dylan E Booth, Christopher M Sullivan, Richard Aggarwal, Ajay BMJ Research OBJECTIVE: To quantify the association of cancer treatment delay and mortality for each four week increase in delay to inform cancer treatment pathways. DESIGN: Systematic review and meta-analysis. DATA SOURCES: Published studies in Medline from 1 January 2000 to 10 April 2020. ELIGIBILITY CRITERIA FOR SELECTING STUDIES: Curative, neoadjuvant, and adjuvant indications for surgery, systemic treatment, or radiotherapy for cancers of the bladder, breast, colon, rectum, lung, cervix, and head and neck were included. The main outcome measure was the hazard ratio for overall survival for each four week delay for each indication. Delay was measured from diagnosis to first treatment, or from the completion of one treatment to the start of the next. The primary analysis only included high validity studies controlling for major prognostic factors. Hazard ratios were assumed to be log linear in relation to overall survival and were converted to an effect for each four week delay. Pooled effects were estimated using DerSimonian and Laird random effect models. RESULTS: The review included 34 studies for 17 indications (n=1 272 681 patients). No high validity data were found for five of the radiotherapy indications or for cervical cancer surgery. The association between delay and increased mortality was significant (P<0.05) for 13 of 17 indications. Surgery findings were consistent, with a mortality risk for each four week delay of 1.06-1.08 (eg, colectomy 1.06, 95% confidence interval 1.01 to 1.12; breast surgery 1.08, 1.03 to 1.13). Estimates for systemic treatment varied (hazard ratio range 1.01-1.28). Radiotherapy estimates were for radical radiotherapy for head and neck cancer (hazard ratio 1.09, 95% confidence interval 1.05 to 1.14), adjuvant radiotherapy after breast conserving surgery (0.98, 0.88 to 1.09), and cervix cancer adjuvant radiotherapy (1.23, 1.00 to 1.50). A sensitivity analysis of studies that had been excluded because of lack of information on comorbidities or functional status did not change the findings. CONCLUSIONS: Cancer treatment delay is a problem in health systems worldwide. The impact of delay on mortality can now be quantified for prioritisation and modelling. Even a four week delay of cancer treatment is associated with increased mortality across surgical, systemic treatment, and radiotherapy indications for seven cancers. Policies focused on minimising system level delays to cancer treatment initiation could improve population level survival outcomes. BMJ Publishing Group Ltd. 2020-11-04 /pmc/articles/PMC7610021/ /pubmed/33148535 http://dx.doi.org/10.1136/bmj.m4087 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research
Hanna, Timothy P
King, Will D
Thibodeau, Stephane
Jalink, Matthew
Paulin, Gregory A
Harvey-Jones, Elizabeth
O’Sullivan, Dylan E
Booth, Christopher M
Sullivan, Richard
Aggarwal, Ajay
Mortality due to cancer treatment delay: systematic review and meta-analysis
title Mortality due to cancer treatment delay: systematic review and meta-analysis
title_full Mortality due to cancer treatment delay: systematic review and meta-analysis
title_fullStr Mortality due to cancer treatment delay: systematic review and meta-analysis
title_full_unstemmed Mortality due to cancer treatment delay: systematic review and meta-analysis
title_short Mortality due to cancer treatment delay: systematic review and meta-analysis
title_sort mortality due to cancer treatment delay: systematic review and meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7610021/
https://www.ncbi.nlm.nih.gov/pubmed/33148535
http://dx.doi.org/10.1136/bmj.m4087
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