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Role of Activin A (ActA) in the Human Cancer Cachexia

Role of Activin A (ActA) in the Human Cancer Cachexia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01604642
Enrollment
150
Registered
2012-05-24
Start date
2012-05-31
Completion date
2016-01-01
Last updated
2018-04-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer, Lung Cancer

Brief summary

The goal of the investigators study is to investigate the role of a hormone named Activin A (ActA) in the development of the skeletal muscle atrophy caused by cancer. According to the investigators hypothesis, ActA could be released by the tumor and activate a muscle atrophy gene program. To answer this question, the investigators plan first to compare circulating levels of ActA in cancer patients with and without cachexia. In a second step, the investigators would like to assess whether ActA circulating levels are predictive for the development of cachexia and short survival.

Interventions

OTHERblood tests and muscular biopsies

blood tests and muscular biopsies

Sponsors

Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18-year-old or older * Colorectal or lung cancer demonstrated by histology or cytology * New diagnosis or new recurrence * Expected survival more than 3 months * No previous history of other cancer in the last 5 years * No pregnancy or lactation * Signed informed consent

Exclusion criteria

* Non-caucasian * Major digestive malabsorption * Major depression * Artificial nutrition * Height doses of steroids (\>1 mg/kg hydrocortisone equivalent) * Hyperthyroidism * Other causes of malnutrition * Expected survival less than 3 months * Severely impaired walking * Anticoagulants or antiplatelet therapy * Disability or medical condition which might prevent the compliance to the protocol * Any conditions which may prevent the compliance to the protocol * Performance status ECOG \> ou = 4 * Participation to other clinical studies

Design outcomes

Primary

MeasureTime frame
Circulating Activin A level2 years

Secondary

MeasureTime frame
Body mass index2 years
Mid arm muscle circumference calculated by the triceps skinfold and the mid arm circumference2 years
Dietary assessment measured by SNAQ score and 3-Day intake2 years
Muscle strength as measured by grip strength2 years
Quality of life as assessed using the QLQ-C302 years
Body composition measured by bioimpedance2 years

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026