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Use of β-hydroxy-β-methylbutyrate to Counteract Muscle Loss in Men With Prostate Cancer on Androgen Ablation

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Standard of care ADT + (HMB + arginine + glutamine)
Standard of care ADT
Sponsored by
Medical College of Wisconsin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Prostate Cancer focused on measuring Prostate Cancer, Men, Androgen Deprivation Therapy, Elderly, Geriatric, Nutritional supplementation

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Histologically confirmed adenocarcinoma of the prostate
  2. Age 60 years or older
  3. Patients with asymptomatic or minimally symptomatic PCa for which they are about to start androgen deprivation therapy (ADT) per provider recommendation

    • Asymptomatic or minimally symptomatic (as judged by treating physician) metastases allowed
    • Men receiving ADT for localized prostate cancer are allowed
  4. Patient able to give informed consent.

Exclusion Criteria:

  1. Patient already on ADT
  2. Patients who are visiting clinic for a second opinion only
  3. Patients with a diagnosis of dementia
  4. Patients with a diagnosis of a neuromuscular disorder (i.e. multiple sclerosis)

Sites / Locations

  • Froedtert Hospital and the Medical College of Wisconsin

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Standard of care ADT + (HMB + AG)

Standard of care ADT

Arm Description

Standard of care androgen deprivation therapy plus the nutritional supplement HMB + arginine + glutamine (AG)

Standard of care androgen deprivation therapy

Outcomes

Primary Outcome Measures

Change From Baseline in Body Composition (Lean Body Mass)
This measure will be the change of lean body mass from baseline reported in kilograms.

Secondary Outcome Measures

Change From Baseline of Dorsiflexor Muscle Size in mm^2.
Cross-sectional area of the dorsiflexor muscle will be measured in mm^2 using magnetic resonance imaging. The dorsiflexor muscles at the front of the leg are responsible for lifting the ball of the foot with the heel in contact with the ground. One dorsiflexor muscle in one leg was analyzed per participant.
Change From Baseline in Strength of the Dorsiflexor Muscle in Kilograms.
Dorsiflexor muscle strength in kilograms will be measured with a custom lower leg ergometer. The dorsiflexor muscles at the front of the leg are responsible for lifting the ball of the foot with the heel in contact with the ground.
Physical Performance Measured Using the Short Physical Performance Battery (SPPB)
The SPPB uses Likert-style ratings for balance, walking speed, and standing test (Guralnik, 2000). Balance metric is the ability to hold three standing positions (feet side-by-side; side of the heel of one foot touching the big toe of the other foot; heel of one foot in front of and touching the toes of the other) up to 10 seconds. Inability to hold a position scores '0'. The sum of scores is the Balance Score. Scoring range is 0-4. Higher scores indicate better balance. Walking metric is time to walk 8 feet. Faster times score more points. Inability to complete the walk scores '0'. The score range is 0-4. Higher scores indicate better mobility. The Standing Test. The subject is asked to stand and sit five times as quickly as possible. Inability to complete five repetitions scores '0'. Shorter times score more points. Scoring range is 0-4. Higher scores indicate better mobility. Overall score is the sum of the scores ranging 0 to 12. Higher scores indicate better performance.
Change From Baseline in the Number of Fall Events
This measure will be the change in the number of reported falls from baseline (defined as the 3 months preceding the baseline visit), and the 3 month period beginning after the baseline visit and continuing through 3 months of therapy.

Full Information

First Posted
April 20, 2012
Last Updated
September 20, 2023
Sponsor
Medical College of Wisconsin
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1. Study Identification

Unique Protocol Identification Number
NCT01607879
Brief Title
Use of β-hydroxy-β-methylbutyrate to Counteract Muscle Loss in Men With Prostate Cancer on Androgen Ablation
Official Title
Use of β-hydroxy-β-methylbutyrate to Counteract Loss of Muscle Mass and Strength in Older Men With Prostate Cancer Started on Androgen Deprivation Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
March 2014 (undefined)
Primary Completion Date
July 2018 (Actual)
Study Completion Date
February 16, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical College of Wisconsin

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a study of HMB plus amino acids in older men with prostate cancer starting androgen deprivation therapy (ADT). The investigators hypothesize that the use of this nutritional supplementation will decrease the loss of muscle mass and strength that occurs when men start ADT.
Detailed Description
It is well established that older patients experience age-related loss of muscle mass and function (sarcopenia), presumably due to an imbalance of protein synthesis versus protein breakdown. In addition, studies have shown that men who start on ADT experience increased muscle protein breakdown and decreased synthesis. β-hydroxy-β-methylbutyrate (HMB), a leucine metabolite, has been shown to slow protein breakdown. When HMB is given with arginine and lysine (which support protein synthesis) in randomized trials, researchers have shown that elderly men and women who receive this nutritional supplementation experience improvement in fat-free mass, strength, functionality and protein synthesis when compared with controls. In addition, patients with advanced cancer who experienced weight loss of at least 5% have also been shown to benefit from HMB, with supplementation resulting in a significant increase of fat-free mass when compared to controls. Thus, it seems reasonable that older men with prostate cancer starting on ADT who experience lean muscle loss as a result of aging and ADT, may achieve some benefit from supplementation with HMB as well. Use of HMB in men with prostate cancer has not been reported.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate Cancer, Men, Androgen Deprivation Therapy, Elderly, Geriatric, Nutritional supplementation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard of care ADT + (HMB + AG)
Arm Type
Experimental
Arm Description
Standard of care androgen deprivation therapy plus the nutritional supplement HMB + arginine + glutamine (AG)
Arm Title
Standard of care ADT
Arm Type
Active Comparator
Arm Description
Standard of care androgen deprivation therapy
Intervention Type
Drug
Intervention Name(s)
Standard of care ADT + (HMB + arginine + glutamine)
Other Intervention Name(s)
Juven
Intervention Description
1 packet of HMB+arginine+glutamine contains 1.5 g of the amino acid metabolite HMB + 7 g arginine and 7 g glutamine. Take one packet twice daily for 3 months
Intervention Type
Other
Intervention Name(s)
Standard of care ADT
Other Intervention Name(s)
Standard of care androgen deprivation therapy (ADT)
Intervention Description
Patient will receive standard of care androgen deprivation therapy (ADT) alone
Primary Outcome Measure Information:
Title
Change From Baseline in Body Composition (Lean Body Mass)
Description
This measure will be the change of lean body mass from baseline reported in kilograms.
Time Frame
Baseline, 3 months
Secondary Outcome Measure Information:
Title
Change From Baseline of Dorsiflexor Muscle Size in mm^2.
Description
Cross-sectional area of the dorsiflexor muscle will be measured in mm^2 using magnetic resonance imaging. The dorsiflexor muscles at the front of the leg are responsible for lifting the ball of the foot with the heel in contact with the ground. One dorsiflexor muscle in one leg was analyzed per participant.
Time Frame
Baseline and 3 months
Title
Change From Baseline in Strength of the Dorsiflexor Muscle in Kilograms.
Description
Dorsiflexor muscle strength in kilograms will be measured with a custom lower leg ergometer. The dorsiflexor muscles at the front of the leg are responsible for lifting the ball of the foot with the heel in contact with the ground.
Time Frame
Baseline and 3 months
Title
Physical Performance Measured Using the Short Physical Performance Battery (SPPB)
Description
The SPPB uses Likert-style ratings for balance, walking speed, and standing test (Guralnik, 2000). Balance metric is the ability to hold three standing positions (feet side-by-side; side of the heel of one foot touching the big toe of the other foot; heel of one foot in front of and touching the toes of the other) up to 10 seconds. Inability to hold a position scores '0'. The sum of scores is the Balance Score. Scoring range is 0-4. Higher scores indicate better balance. Walking metric is time to walk 8 feet. Faster times score more points. Inability to complete the walk scores '0'. The score range is 0-4. Higher scores indicate better mobility. The Standing Test. The subject is asked to stand and sit five times as quickly as possible. Inability to complete five repetitions scores '0'. Shorter times score more points. Scoring range is 0-4. Higher scores indicate better mobility. Overall score is the sum of the scores ranging 0 to 12. Higher scores indicate better performance.
Time Frame
Baseline and 3 months
Title
Change From Baseline in the Number of Fall Events
Description
This measure will be the change in the number of reported falls from baseline (defined as the 3 months preceding the baseline visit), and the 3 month period beginning after the baseline visit and continuing through 3 months of therapy.
Time Frame
Baseline, 3 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed adenocarcinoma of the prostate Age 60 years or older Patients with asymptomatic or minimally symptomatic prostate cancer for which they are about to start androgen deprivation therapy (ADT) per provider recommendation Asymptomatic or minimally symptomatic (as judged by treating physician) metastases allowed Men receiving ADT for localized prostate cancer are allowed Patient able to give informed consent. Exclusion Criteria: Patient already on ADT Patients who are visiting clinic for a second opinion only Patients with a diagnosis of dementia Patients with a diagnosis of a neuromuscular disorder (i.e. multiple sclerosis)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathryn Bylow, MD
Organizational Affiliation
Medical College of Wisconsin
Official's Role
Principal Investigator
Facility Information:
Facility Name
Froedtert Hospital and the Medical College of Wisconsin
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53226
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
10811152
Citation
Guralnik JM, Ferrucci L, Pieper CF, Leveille SG, Markides KS, Ostir GV, Studenski S, Berkman LF, Wallace RB. Lower extremity function and subsequent disability: consistency across studies, predictive models, and value of gait speed alone compared with the short physical performance battery. J Gerontol A Biol Sci Med Sci. 2000 Apr;55(4):M221-31. doi: 10.1093/gerona/55.4.m221.
Results Reference
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Use of β-hydroxy-β-methylbutyrate to Counteract Muscle Loss in Men With Prostate Cancer on Androgen Ablation

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