Cachexia is a frequently observed syndrome in cancer patients. It reversely impacts quality of life and is linearly and prognostically related to clinical outcome but cannot be fully reversed by conventional nutritional therapy. In contrast to…
ID
Bron
Aandoening
precachexia, cachexia, cancer
precachexie, cachexie, kanker
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
To determine the prevalence of (pre)cachexia (based on the current definition) in patients with advanced cancer scheduled for treatment with chemotherapy.
Achtergrond van het onderzoek
Cachexia is a frequently observed syndrome in cancer patients. It reversely impacts quality of life and is linearly and prognostically related to clinical outcome but cannot be fully reversed by conventional nutritional therapy. In contrast to cachexia, pre-cachexia is expected to be a still reversible state that may respond to nutritional intervention. Recently, an expert-opinion of pre-cachexia has been put forward that can be used for the early identification, and subsequently for the early treatment, of pre-cachexia. The current proposal aims to study the prevalence of pre-cachexia and cachexia, to identify patient groups at increased risk and to explore potential biomarkers of pre-cachexia.
Doel van het onderzoek
Cachexia is a frequently observed syndrome in cancer patients. It reversely impacts quality of life and is linearly and prognostically related to clinical outcome but cannot be fully reversed by conventional nutritional therapy. In contrast to cachexia, pre-cachexia is expected to be a still reversible state that may respond to nutritional intervention. Recently, an expert-opinion of pre-cachexia has been put forward that can be used for the early identification, and subsequently for the early treatment, of pre-cachexia. The current proposal aims to study the prevalence of pre-cachexia and cachexia, to identify patient groups at increased risk and to explore potential biomarkers of pre-cachexia.
Onderzoeksopzet
Cross-sectional design (try for 2 measurements with one week in between).
Onderzoeksproduct en/of interventie
Two interviews of at maximum 30 minutes (with one week in between), including 3 small self-administered questionnaires, 2 VAS-scales and a measurement of body composition. In addition, 60 patients with stage III/IV non-small cell lung cancer are asked for extra blood collection during (two tubes) routinely collected blood in fasted state to identify potential biomarkers of pre-cachexia and cachexia.
Publiek
P.O. Box 7057
M.A.E. Bokhorst - de van der Schueren, van
De Boelelaan 1117
Amsterdam 1007 MB
The Netherlands
m.vanbokhorst@vumc.nl
Wetenschappelijk
P.O. Box 7057
M.A.E. Bokhorst - de van der Schueren, van
De Boelelaan 1117
Amsterdam 1007 MB
The Netherlands
m.vanbokhorst@vumc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
4.2.1 Inclusion criteria for cohort (part 1, not-WMO):
1. Adults (> 18 years);
2. Advanced breast cancer, colorectal cancer, hormone refractory prostate cancer or stage III/IV non small cell lung cancer;
3. Treatment plan: Palliative chemotherapy or in the case of stage III NSCLC: chemoradiation.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Ascites (for which treatment is necessary) or serious pitting edema;
2. Chemotherapy treatment in the past month;
3. Not able to speak the Dutch language;
4. Pregnancy.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL2947 |
NTR-old | NTR3094 |
CCMO | NL37535.029.11 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |
OMON | NL-OMON35709 |