Small-intestine Neuroendocrine Tumors (Carcinoid Tumors)
Conditions
Brief summary
Urinary measure of 5-hydroxyindolacetic acid (5HIAA) is an important marker for the diagnosis and follow-up of patients with small-intestine neuroendocrine tumors. Although this marker has good specificity, its sensitivity is moderate and its dosage is constraining, since it requires urine collection over 2-3 days and specific diet. Preliminary data suggested that overnight 5HIAA value may be representative of 24-hour 5HIAA value, and that plasma 5HIAA dosage could be a valuable alternative to urine 5HIAA dosage. The main objective of this study is to compare sensitivity and specificity of overnight 5HIAA value, 24-hour 5HIAA value and plasma 5HIAA value, in patients with small-intestine neuroendocrine tumors.
Detailed description
This study primarily aims at comparing the sensitivity and specificity of overnight 5HIAA value, 24-hour 5HIAA value and plasma 5HIAA value, in patients with small-intestine neuroendocrine tumors. Secondary objectives include the correlation of 5HIAA values with chromogranin A, carcinoid syndrome and tumor burden and the evaluation of the compliance to the diet and its correlation with 5HIAA values. The study group will include patients with proven neuroendocrine tumors of various stages and functioning syndrome profile. A control group will be constituted with subjects having irritable bowel syndrome, in which a neuroendocrine tumor is ruled out. After providing informed consent, patients fitting with inclusion criteria will be included in the study. Patients will have to follow a specific diet, and interrupt/avoid certain medication, during the 2 days before and the 2 days during the sampling period. Whole urine samples will be collected during 2 consecutive days, in 4 parts (day1, night 1, day 2, night 2). Blood samples will be collected at the morning of days 2 and 3. Observance with diet and drug restriction will be evaluated at the morning of day 3.
Interventions
BIOLOGICALblood sample withdrawn
Sponsors
CHU de Reims
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No
Inclusion criteria
* Histologically proven small-intestine neuroendocrine tumors, at initial diagnosis or during the follow-up * Irritable bowel syndrome, diagnosed following Rome III criteria, who had an ileo-colonoscopy and an abdominal CT-scan within the 12 last months * Age \> 18 years * No antitumor treatment within the last three months excepted somatostatin analogs * Ability of understanding and approving the study protocol and of providing written consent * Affiliation to the French Health Social System
Exclusion criteria
* Small-intestine neuroendocrine tumor in remission (no detectable disease) * Other malignancies than small-intestine neuroendocrine tumors (excepted if in remission for more than 2 years) * Kidney insufficiency (MDRD \< 60/min) * Urinary incontinency or inability to collect urines * Any antitumor treatment within the last three months excepted somatostatin analogs * Inability to interrupt treatments interfering with 5HIAA dosage * Pregnancy * Patients under law protection
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| urine 5HIAA value | 24-hour |
Countries
France
Outcome results
None listed