Actively Recruiting
Biomoleculars Markers of Sensitivity to Pre- and Post-operative Chemotherapy of Gastric and Cardia Adenocarcinomas: a Pilot Study
Led by University Hospital, Strasbourg, France · Updated on 2025-08-08
80
Participants Needed
1
Research Sites
691 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Some subtypes of gastric and cardia tumors such as adenocarcinoma or gastric linitis with disseminated cells respond poorly to the pre-operative chemotherapy, and some of them do not respond to chemotherapy usually performed. Doing chemotherapy in these patients could delay their surgical management. The completion of chemotherapy for these patients would be a bad prognosis factor according to recent data from the literature. Therefore, the aim of this research is to find prognostic markers of sensitivity to chemotherapy usually performed. The investigators are going to use biopsies realized at diagnosis and select patients "good and bad" responders. Primary purpose: To study cardia and gastric tumors, molecular markers sensitivity to pre- and post- perative chemotherapy protocols (EOX protocol ... FOLFOX) or chemoradiation Secondary purposes: * To assess the impact of patients' lifestyle (via a questionnaire) on the response to chemotherapy * To study markers of cancer stem cells * To correlate clinical and molecular markers with patient survival and quality of life questionnaires * To characterize the expression levels (Met, Her2, FGFR2) and mutations (p53 ras) in frequently deregulated genes in gastric cancers. * To characterize the level of expression of predictive candidate markers (ΔNp73, TAp73, HDAC4, mir140, EZH2, CXCL12, CXCR4, CXCR7) found in the literature. * To correlate the abnormalities found in the with tumor stages (before and after chemotherapy) and with 5 years overall survival and progression-free patients
CONDITIONS
Official Title
Biomoleculars Markers of Sensitivity to Pre- and Post-operative Chemotherapy of Gastric and Cardia Adenocarcinomas: a Pilot Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of gastric adenocarcinoma (any location) or cardia adenocarcinoma
- Age greater than 18 years
- WHO performance status index less than or equal to 3
- Signed informed consent form
You will not qualify if you...
- Having other cancers currently treated with chemotherapy
- Pregnant or breastfeeding
- Difficulty understanding study information or instructions
AI-Screening
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Trial Site Locations
Total: 1 location
1
University Hospital, Strasbourg, france
Strasbourg, France, 67000
Actively Recruiting
Research Team
B
Benoît ROMAIN, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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