Molecular Profiling for Appendiceal Cancer
This study is looking at archived tumor tissue from people with appendiceal cancer or appendiceal adenocarcinoma. Researchers are using two tests, DNA Methylation Profiling and m6A Epitranscriptomic Profiling, to understand the cancer's molecular makeup. The goal is to find new ways to predict how the cancer might behave and to improve how doctors categorize the disease. This could help doctors better understand your specific cancer and guide treatment decisions. The study will measure how long people live (Overall Survival) and how long they live without the cancer getting worse (Progression-Free Survival) over about one year. The current status of the study is unclear.
- Study design
- This is an observational study, meaning researchers are looking at existing information rather than giving new treatments. It plans to include 400 participants.
- What's involved
- You would need to have archived tumor tissue available that is suitable for molecular profiling. You would also need to have relevant medical information available.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants' overall survival and progression-free survival will be measured through study completion, an average of 1 year.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Molecular Profiling for Risk Stratification in Appendiceal Cancer
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Overall SurvivalThrough study completion, an average of 1 year
Overall survival will be evaluated in relation to molecular profiling results and available clinicopathologic characteristics. Survival analyses may include Kaplan-Meier analysis and Cox proportional hazards models
- Progression-Free SurvivalThrough study completion, an average of 1 year
Progression-free survival will be evaluated in relation to molecular profiling results and available clinicopathologic characteristics. Time-to-event analyses may be performed using standard survival analysis methods.