Prehabilitation in Liver Surgery

Sponsor
Liverpool University Hospitals NHS Foundation Trust (Other)
Overall Status
Completed
CT.gov ID
NCT01523353
Collaborator
(none)
37
1
2
23
1.6

Study Details

Study Description

Brief Summary

Each year in the UK around 1500 patients undergo surgery for bowel cancer that has spread to the liver. This is major surgery that offers a chance of cure, but can be associated with complications. Fitter patients are less likely to have serious complications. We are interested in finding out whether a short exercise program can improve patient fitness before surgery and whether this can reduce surgical complications.

We plan to measure the fitness of patients who are going to have liver surgery. We will then give them an exercise programme for 4 weeks, after which we will assess their fitness again.

We are also interested in whether fitter people have better Liver function. To assess this we will take a small sample of liver tissue during the operation for laboratory analysis of its function.

Hypothesis

  1. A short period of exercise can significantly improve fitness prior to liver surgery

  2. Greater Fitness is associated with better liver function.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exercise Intervention
Phase 1

Detailed Description

Prehabilitation in Liver Surgery

Introduction Thirty per cent of patients with colorectal cancer have metastatic disease at time of presentation, and a further 20% will develop liver metastases after the primary colorectal malignancy has been resected. Liver resection offers the prospect of cure for a proportion of these patients and, with the increasing use of effective neo-adjuvant chemotherapy, this proportion is increasing. However, liver surgery is associated with significant morbidity and mortality and this may be higher in patients with comorbidity, poor cardiorespiratory fitness and in those who have received neo-adjuvant chemotherapy.

Cardiopulmonary exercise testing (CPET) is a non-invasive assessment of cardiovascular and pulmonary function, which can be quantified by measures such as anaerobic threshold (AT) and VO2peak. The anaerobic threshold is a measure of sustainable exercise, where the VO2peak is a measure of maximal exercise capacity. The AT has been assessed in different surgical groups and has been shown as a useful predictor of postoperative complications and survival. Early work has demonstrated that short periods of preoperative exercise intervention can improve AT and VO2peak. However, no work has to date been undertaken in patients prior to liver surgery.

Hepatic glucose metabolism provides much of the energy requirements of the postoperative period. Work has demonstrated that exercise training increases hepatic glucose production, and that its inhibition has a marked effect on endurance capability. This may be particularly relevant when surgical resections can involve resection of up to 80% of hepatic tissue. However, a link between hepatic gluconeogenic capacity and fitness as assessed by cardiopulmonary exercise testing has not been established.

A demonstrable link between gluconeogenic capacity and cardiopulmonary fitness and an explanation of its underpinning physiology would help explain some of the systemic effects of drug hepatotoxicity. It would also allow development of strategies to improve gluconeogenic capacity that may reduce complications and improve tolerance of many hepatoxic agents such as chemotherapy.

Hypothesis

  1. A short exercise program can significantly improve the CPET defined anaerobic threshold prior to liver surgery in a cancer population and this will be associated with reduced post-operative morbidity and mortality.

  2. Hepatic gluconeogenic capacity will be associated with cardiopulmonary fitness.

  3. Gluconeogenic capacity will be associated with mitochondrial number and quantity of enzymes which are integral to gluconeogenesis such as PEPCK

Methods Patients with colorectal liver metastases suitable for hepatic resection will undergo a baseline CPET and then be randomised to either preoperative exercise intervention or standard care. Patients within the intervention arm will undergo a 4 week exercise program consisting of 3 interval sessions per week on a stationary bike. This will be individually tailored according to their initial exercise test. In the week prior to surgery all patients will then undergo a further CPET. At surgery liver tissue will be taken to determine hepatic gluconeogenic capacity. CPET tests will then be performed where possible in patients at 6 weeks and 3 months following surgery. Post-operative complications (Clavien classification and Postoperative morbidity score (POMS)) and 30 and 90-day mortality will be recorded. Quality of life assessments (EORTC/SF-36) will be taken at recruitment, the week prior to surgery, 6 weeks after surgery and 3 months following surgery.

Laboratory Analysis Hepatic gluconeogenic capacity will be assessed by direct analysis of fresh slices of hepatic tissue taken at the time of surgery. Slices will be taken using the Krumdiek MD6000 tissue slicer. These will be weighed an incubated in a buffer containing lactate. Glucose will be measured using the Glucose Oxidase assay, and calculated per mg wet weight of hepatic tissue. Further analysis of mitochondrial number and ATP production, and enzymatic levels will be conducted following initial results.

Statistical considerations This is a study of a continuous response variable from matched pairs of study subjects and will need 38 patients to detect a true difference 1.5ml/min/kg, with a probability 0.8 and Type I error 0.05). Anticipated recruitment period is 10 months assuming a dropout rate of 20%. Randomisation is by computerised block randomisation, and patients will be stratified by receipt of neo-adjuvant chemotherapy.

Study Design

Study Type:
Interventional
Actual Enrollment :
37 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Care Provider, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Feasibility Study of Preoperative Exercise Intervention in the Resection of Colorectal Liver Metastasis.
Study Start Date :
Jul 1, 2011
Actual Primary Completion Date :
Jun 1, 2013
Actual Study Completion Date :
Jun 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Exercise Intervention

4 week personalised exercise program on a static bicycle.

Behavioral: Exercise Intervention
4 week personalised exercise program on a static cycle. Supervised in a hospital environment

No Intervention: Control Arm

Patients having standard preoperative preparation and advice.

Outcome Measures

Primary Outcome Measures

  1. Anaerobic threshold prior to liver resection [4 weeks]

    This is a measure of cardiopulmonary fitness as detected by a cardiopulmonary exercise test.

Secondary Outcome Measures

  1. Hospital Length of stay [6 weeks]

    length of hospital admission from date of surgery

  2. Post operative morbidity [3 months]

    As measured using Clavien classification and postoperative morbidity scores

  3. Quality of Life [4 months]

    SF -36 and EORTC questionaires at 5 weeks, 6 weeks postoperatively, and 3 months postoperatively

  4. Mortality [30 day and 90 day postoperative]

  5. Attendance at exercise sessions [6 weeks]

  6. Serious adverse events within exercise program [6 weeks]

    The investigators are not expecting and serious adverse events during the program.

  7. other measures of cardiopulmonary function [6 weeks]

    Detected by cardiopulmonary exercise prior to surgery.

  8. Recovery of fitness [6 and 12 weeks post operatively]

    recovery of cardiopulmonary exercise test determined fitness post surgery.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Planned resection of colorectal liver metastasis

  • Able to perform cycle based exercise program

  • Age over 18

Exclusion Criteria:
  • Unable to consent

  • Unable to perform cycle based exercise program

  • Age under 18

Contacts and Locations

Locations

Site City State Country Postal Code
1 Aintree University Hospital Liverpool Merseyside United Kingdom L9 7AL

Sponsors and Collaborators

  • Liverpool University Hospitals NHS Foundation Trust

Investigators

  • Principal Investigator: Declan FJ Dunne, MBChB(Hons), Liverpool University Hospitals NHS Foundation Trust

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Declan Dunne, Surgical Research Fellow, Liverpool University Hospitals NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT01523353
Other Study ID Numbers:
  • 11/H1005/3
First Posted:
Feb 1, 2012
Last Update Posted:
Dec 17, 2013
Last Verified:
Feb 1, 2012
Keywords provided by Declan Dunne, Surgical Research Fellow, Liverpool University Hospitals NHS Foundation Trust
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 17, 2013