Exercise prehabilitation during neoadjuvant chemotherapy may enhance tumour regression in oesophageal cancer: results from a prospective non-randomised trial.


Journal

British journal of sports medicine
ISSN: 1473-0480
Titre abrégé: Br J Sports Med
Pays: England
ID NLM: 0432520

Informations de publication

Date de publication:
Apr 2022
Historique:
accepted: 06 12 2021
pubmed: 3 2 2022
medline: 22 3 2022
entrez: 2 2 2022
Statut: ppublish

Résumé

There is increasing evidence for the use of exercise in cancer patients and data supporting enhanced tumour volume reduction following chemotherapy in animal models. To date, there is no reported histopathological evidence of a similar oncological benefit in oesophageal cancer. A prospective non-randomised trial compared a structured prehabilitation exercise intervention during neoadjuvant chemotherapy and surgery versus conventional best-practice for oesophageal cancer patients. Biochemical and body composition analyses were performed at multiple time points. Outcome measures included radiological and pathological markers of disease regression. Logistic regression calculated ORs with 95% CI for the likelihood of pathological response adjusting for chemotherapy regimen and chemotherapy delivery. Comparison of the Intervention (n=21) and Control (n=19) groups indicated the Intervention group had higher rates of tumour regression (Mandard TRG 1-3 Intervention n=15/20 (75%) vs Control n=7/19 (36.8%) p=0.025) including adjusted analyses (OR 6.57; 95% CI 1.52 to 28.30). Combined tumour and node downstaging (Intervention n=9 (42.9%) vs Control n=3 (15.8%) p=0.089) and Fat Free Mass index were also improved (Intervention 17.8 vs 18.7 kg/m The results suggest improved tumour regression and downstaging in the exercise intervention group and should prompt larger studies on this topic. NCT03626610.

Sections du résumé

BACKGROUND BACKGROUND
There is increasing evidence for the use of exercise in cancer patients and data supporting enhanced tumour volume reduction following chemotherapy in animal models. To date, there is no reported histopathological evidence of a similar oncological benefit in oesophageal cancer.
METHODS METHODS
A prospective non-randomised trial compared a structured prehabilitation exercise intervention during neoadjuvant chemotherapy and surgery versus conventional best-practice for oesophageal cancer patients. Biochemical and body composition analyses were performed at multiple time points. Outcome measures included radiological and pathological markers of disease regression. Logistic regression calculated ORs with 95% CI for the likelihood of pathological response adjusting for chemotherapy regimen and chemotherapy delivery.
RESULTS RESULTS
Comparison of the Intervention (n=21) and Control (n=19) groups indicated the Intervention group had higher rates of tumour regression (Mandard TRG 1-3 Intervention n=15/20 (75%) vs Control n=7/19 (36.8%) p=0.025) including adjusted analyses (OR 6.57; 95% CI 1.52 to 28.30). Combined tumour and node downstaging (Intervention n=9 (42.9%) vs Control n=3 (15.8%) p=0.089) and Fat Free Mass index were also improved (Intervention 17.8 vs 18.7 kg/m
CONCLUSION CONCLUSIONS
The results suggest improved tumour regression and downstaging in the exercise intervention group and should prompt larger studies on this topic.
TRIAL REGISTRATION NUMBER BACKGROUND
NCT03626610.

Identifiants

pubmed: 35105604
pii: bjsports-2021-104243
doi: 10.1136/bjsports-2021-104243
doi:

Banques de données

ClinicalTrials.gov
['NCT03626610']

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

402-409

Informations de copyright

© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Janine Zylstra (J)

Gastrointestinal Medicine and Surgery, Guy's and St Thomas' Hospitals NHS Trust, London, UK.
School of Sport and Exercise Science, Liverpool John Moores University, Liverpool, UK.

Greg P Whyte (GP)

School of Sport and Exercise Science, Liverpool John Moores University, Liverpool, UK.
Research Institute for Sport and Exercise Science, Liverpool John Moores University, Liverpool, UK.
Centre for Health and Human Performance, London, UK.

Kerri Beckmann (K)

School of Cancer and Pharmaceutical Studies, King's College London, London, UK.

James Pate (J)

Centre for Health and Human Performance, London, UK.

Aida Santaolalla (A)

School of Cancer and Pharmaceutical Studies, King's College London, London, UK.

Louise Gervais-Andre (L)

Clinical Cancer Imaging, King's College London, London, UK.

Beth Russell (B)

School of Cancer and Pharmaceutical Studies, King's College London, London, UK.

Nick Maisey (N)

Oncology, Guy's and St Thomas' Hospitals NHS Trust, London, UK.

Justin Waters (J)

Oncology, Maidstone and Tunbridge Wells NHS Trust, Maidstone, UK.

Gemma Tham (G)

Physiotherapy, Guy's and St Thomas' Hospitals NHS Trust, London, UK.

Jesper Lagergren (J)

School of Cancer and Pharmaceutical Studies, King's College London, London, UK.

Michael Green (M)

Pathology, Guy's and St Thomas' Hospitals NHS Trust, London, UK.

Mark Kelly (M)

Gastrointestinal Medicine and Surgery, Guy's and St Thomas' Hospitals NHS Trust, London, UK.

Cara Baker (C)

Gastrointestinal Medicine and Surgery, Guy's and St Thomas' Hospitals NHS Trust, London, UK.

Mieke Van Hemelrijck (M)

School of Cancer and Pharmaceutical Studies, King's College London, London, UK.

Vicky Goh (V)

Clinical Cancer Imaging, King's College London, London, UK.

James Gossage (J)

Gastrointestinal Medicine and Surgery, Guy's and St Thomas' Hospitals NHS Trust, London, UK.

Mike Browning (M)

Anaesthesia and Intensive Care Medicine, Maidstone and Tunbridge Wells Hospital NHS Trust, Maidstone, UK.

Andrew Davies (A)

Gastrointestinal Medicine and Surgery, Guy's and St Thomas' Hospitals NHS Trust, London, UK Andrew.Davies1@gstt.nhs.uk.
School of Cancer and Pharmaceutical Studies, King's College London, London, UK.

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Classifications MeSH