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NCT Number: NCT01694602

Non-Invasive Assessment of Skeletal Muscle Loss in Cancer Patients - Phase II

The overall aim of this research is to develop a non-invasive approach to evaluate the production of 3-methylhistidine (3MH)in cancer patients, as a potential means of determining which patients are at high risk for future development of cancer induced skeletal muscle atrophy.

Rationale: The approach is based on the hypothesis that after an oral dose of deuterated 3-methylhistidine (D-3MH), the slope of the terminal portion of the decay curve (> 12 hours post-dosing) for the tracer/tracee (D-3MH/3MH) in the free 3MH pool is proportional to the rate constant for myofibrillar protein degradation and can be determined from spot urine samples.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Texas Medical Branch

Galveston, Texas, 77555-0361, United States

About this study

The long-term objective of this research is to develop a non-invasive approach for assessment of de novo 3MH production in cancer patients early in the course of the disease as a way of assessing which patients are at high risk for future development of skeletal muscle atrophy. The approach is based on: 1) the known increase in de novo production of 3-methylhistidine (3MH) from muscle protein breakdown in said patients as a consequence of their unique disease-host interactions, and 2) earlier demonstration that de novo 3MH production can be measured in vivo using isotope dilution.

During this Phase-II project, we propose to conduct a statistically powerful prospective investigation to demonstrate that measurement of the slope of the terminal decay curve (rate constant) with our approach in newly diagnosed cancer patients predicts future development of muscle wasting. We expect the outcome of the combined Phase-I and Phase-II research to lead to the early identification of elevated muscle catabolism in at-risk patients so that medical intervention can prevent future muscle atrophy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • (1) histological or cytological evidence of NSCLC without curative options;
  • (2) over 18 years of age;
  • (3) patient reported weight loss of ≤5% of usual body weight in the last 6 months;
  • (4) life expectancy of greater than 6 months based on the judgement of treating physician;
  • (5) serum creatinine ≤1.5 times the upper limit of normal; and
  • (6) willing and able to give informed consent.

Exclusion criteria

  • 1) malabsorption, intractable vomiting or gastrointestinal obstruction
  • 2) congestive heart failure
  • 3) edema or ascites
  • 4) liver function test results that will preclude administration of prescribed therapy
  • 5) pregnant, nursing, or, if of child-bearing age, unwilling to use contraceptives

Treatment and study plan

(non-radioactive) Oral deuterated 3-methylhistidine (D-3MH)

Biological

Oral dose of 9.0 mg (50 μmol) TAU-METHYL-L-HISTIDINE (METHYL-D3), Cambridge Isotope Laboratory, Cambridge, Massachusetts.

Primary outcomes

  1. Determination of myofibrillar protein degradation rate constant and slope of terminal decay curve.

    Time frame: Spot urine (multiple) collections between 12 to 17 hours of D-3MH ingestion.

Sponsors and collaborators

Lead sponsor

The University of Texas Medical Branch, Galveston

Other

Registry information

Official study title

Non-Invasive Assessment of Skeletal Muscle Loss in Cancer Patients - Phase 2

Acronym: 3MH-2

Important dates

Study start
2012
Primary completion
2015
Study completion
2015
First posted
Sep 27, 2012
Registry last updated
Jul 2, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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