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EXALT: EXercise Attenuates Liver Tumors Trial (EXALT)

Primary Purpose

Hepatocellular Carcinoma

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Exercise intervention
Sponsored by
Milton S. Hershey Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma focused on measuring liver cancer

Eligibility Criteria

18 Years - 69 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults age >=18 or <70 years
  • Liver transplant candidates (under evaluation or listed for transplant with HCC)
  • Hepatocellular Carcinoma diagnosis (HCC)
  • Complete response to LRT

Exclusion Criteria:

  • Active cardiac symptoms
  • BMI <18 or >45 kg/m2(16)
  • CPT Class B or C liver disease
  • ECOG >2
  • Hepatic decompensation
  • Institutionalized/prisoner
  • Pregnancy
  • Severe medical comorbidities/psychiatric illness

Sites / Locations

  • Penn State Hershey Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Exercise intervention

Standard of Care

Arm Description

The exercise program will be similar to the Exercise in All ChemoTherapy (ENACT) study which combines in-person and home-based strength training and aerobic exercise five days a week.

Subjects are instructed to maintain their current activity level.

Outcomes

Primary Outcome Measures

Feasibility-number of participants able to complete the trial
Defined as completing >80% of the sessions.(46, 47) While this would be expected for patients with cirrhosis,(46) this would be five-fold larger than the proportion of oncology patients receiving systemic treatment who complete other exercise based randomized controlled trials. We expect exercise in subjects with HCC in the background of Child Pugh Turcotte (CPT) Class A cirrhosis without hepatic decompensation (e.g., ascites, hepatic encephalopathy, bleeding gastroesophageal varices) and Eastern Cooperative Oncology Group (ECOG) 0-2 functional status to be feasible.
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Data from previous oncology trials suggest up to 25% of the participants may experience a mild musculoskeletal impairment and zero adverse effects requiring treatment alterations. Pilot exercise-based trials in patients with cirrhosis have demonstrated <5% adverse events.
Acceptability-scientifically adequate
To assess the effectiveness of exercise trials in patients with HCC. The work with the ongoing NASHFit and completed ENACT Trials and the work of others performing exercise-based trials in patients with cirrhosis(50) has established >50% enrollment of subjects approached as a threshold of acceptability.

Secondary Outcome Measures

HCC recurrence
Overall survival
Cancer-free survival
waiting-list mortality
concentration of IL-6
visceral adipose tissue (VAT)
change in body composition

Full Information

First Posted
May 31, 2019
Last Updated
February 21, 2022
Sponsor
Milton S. Hershey Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03979547
Brief Title
EXALT: EXercise Attenuates Liver Tumors Trial
Acronym
EXALT
Official Title
EXALT: EXercise Attenuates Liver Tumors Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Terminated
Why Stopped
Recruitment challenges
Study Start Date
January 3, 2019 (Actual)
Primary Completion Date
September 9, 2021 (Actual)
Study Completion Date
September 9, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Milton S. Hershey Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The overall goal of this proposal is to test the effect of exercise to delay or avert HCC recurrence and gain information regarding the potential molecular mechanisms of HCC tumor inhibition by exercise.
Detailed Description
Primary liver cancer is the leading cause of cancer worldwide. The majority of primary liver cancers are hepatocellular carcinoma (HCC) and occur in the setting of cirrhosis of the liver. Body fat and systemic inflammation are determinants of HCC risk. Cirrhotic patients with HCC are often treated with locoregional therapies including transarterial chemoembolization (TACE) as a bridge to liver transplantation. Despite this, HCC recurrence rates approach 80%. There is a growing body of evidence to suggest the benefit of exercise in cancer patients. Exercise decreases disease recurrence and improves survival in other primary cancers by altering tumor biology and influencing response to treatment. Although animal models suggest biologic plausibility, whether or not exercise prevents HCC recurrence in cancer patients remains unknown. The overall goal of this proposal is to test the effect of exercise to delay or avert HCC recurrence and gain information regarding the potential molecular mechanisms of HCC tumor inhibition by exercise.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma
Keywords
liver cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
perform an interventional pilot trial and randomize 21 subjects who have had a complete response to TACE to a 3-month exercise intervention (n=14) versus standard of care (n=7) where subjects are instructed to maintain their current activity level.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise intervention
Arm Type
Experimental
Arm Description
The exercise program will be similar to the Exercise in All ChemoTherapy (ENACT) study which combines in-person and home-based strength training and aerobic exercise five days a week.
Arm Title
Standard of Care
Arm Type
No Intervention
Arm Description
Subjects are instructed to maintain their current activity level.
Intervention Type
Behavioral
Intervention Name(s)
Exercise intervention
Intervention Description
Moving Through Cancer: A Guide to Exercise for Cancer Survivors" will serve as the framework for an American College of Sports Medicine certified exercise physiologist with additional Cancer Exercise training to teach proper warm up, use of equipment, exercise form, mode of activity, intensity of exercise, flexibility exercises, and cool down.
Primary Outcome Measure Information:
Title
Feasibility-number of participants able to complete the trial
Description
Defined as completing >80% of the sessions.(46, 47) While this would be expected for patients with cirrhosis,(46) this would be five-fold larger than the proportion of oncology patients receiving systemic treatment who complete other exercise based randomized controlled trials. We expect exercise in subjects with HCC in the background of Child Pugh Turcotte (CPT) Class A cirrhosis without hepatic decompensation (e.g., ascites, hepatic encephalopathy, bleeding gastroesophageal varices) and Eastern Cooperative Oncology Group (ECOG) 0-2 functional status to be feasible.
Time Frame
up to 52 weeks
Title
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Description
Data from previous oncology trials suggest up to 25% of the participants may experience a mild musculoskeletal impairment and zero adverse effects requiring treatment alterations. Pilot exercise-based trials in patients with cirrhosis have demonstrated <5% adverse events.
Time Frame
up to 52 weeks
Title
Acceptability-scientifically adequate
Description
To assess the effectiveness of exercise trials in patients with HCC. The work with the ongoing NASHFit and completed ENACT Trials and the work of others performing exercise-based trials in patients with cirrhosis(50) has established >50% enrollment of subjects approached as a threshold of acceptability.
Time Frame
up to 52 weeks
Secondary Outcome Measure Information:
Title
HCC recurrence
Time Frame
3- and 6- month
Title
Overall survival
Time Frame
3- and 6- month
Title
Cancer-free survival
Time Frame
3- and 6- month
Title
waiting-list mortality
Time Frame
3- and 6- month
Title
concentration of IL-6
Time Frame
3- and 6-month
Title
visceral adipose tissue (VAT)
Description
change in body composition
Time Frame
3- and 6-month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults age >=18 or <70 years Liver transplant candidates (under evaluation or listed for transplant with HCC) Hepatocellular Carcinoma diagnosis (HCC) Complete response to LRT Exclusion Criteria: Active cardiac symptoms BMI <18 or >45 kg/m2(16) CPT Class B or C liver disease ECOG >2 Hepatic decompensation Institutionalized/prisoner Pregnancy Severe medical comorbidities/psychiatric illness
Facility Information:
Facility Name
Penn State Hershey Medical Center
City
Hershey
State/Province
Pennsylvania
ZIP/Postal Code
17033
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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EXALT: EXercise Attenuates Liver Tumors Trial

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