RecruitingNCT03048266

Metabolomics and Genetic Diagnosing Pancreatic Neuroendocrine Tumors in MEN1 Patients

Metabolomics and Genetic Diagnosing Pancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1 Patients


Sponsor

M.D. Anderson Cancer Center

Enrollment

629 participants

Start Date

Nov 5, 2015

Study Type

OBSERVATIONAL

Conditions

Summary

Objectives: The aim of the present study is to assess the significance of metabolomics and genetics in diagnosing and survival evaluation for pNET in the periodic follow-up of MEN1 patients. Aim 1: To evaluate the relationship of serum global metabolic profiles with subsequent development of aggressive PNET and evaluate patients survival in a nested case-control study of MEN1 patients who have developed aggressive PNETs (cases) and MEN1 patients who have developed non-aggressive PNETs (controls). Aim 2: Validate the top serum metabolites identified from Aim 1 in MEN1 patients who have developed aggressive PNETs and MEN1 patients who have developed non-aggressive PNETs, using a targeted metabolomics approach. Aim 3: Prospectively identify the potential miRNA biomarkers of serum with miRNA sequencing in MEN1 patients who have developed aggressive PNETs (cases) and MEN1 patients who have developed non-aggressive PNETs (controls). Aim 4: Validate the potential miRNA biomarkers identified from Aim 1 in MEN1 patients who have developed aggressive PNETs and in MEN1 patients who have developed non-aggressive PNETs, using a targeted qRT-PCR approach (in serums), as well as to see the relationship of potential miRNA biomarkers with patients survival.


Eligibility

Plain Language Summary

Simplified for easier understanding

This study investigates whether special blood tests that measure chemical signals (metabolomics) and genetic markers can detect tiny hormone-producing tumors in the pancreas (called pancreatic neuroendocrine tumors, or PNETs) at an early stage in people who have a hereditary condition called MEN1 (Multiple Endocrine Neoplasia type 1) — a syndrome where tumors can develop in multiple hormone-producing glands. **You may be eligible if...** - You have a confirmed diagnosis of MEN1 syndrome, established through clinical features, genetic testing, or family history meeting accepted diagnostic criteria - You do not yet have a known or prior diagnosis of pancreatic neuroendocrine tumors (PNETs) **You may NOT be eligible if...** - No additional exclusion criteria are listed for this study — if you meet the inclusion criteria above, you should discuss participation with your doctor Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

University of Texas MD Anderson Cancer Center

Houston, Texas, United States

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NCT03048266


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