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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02491840
Other study ID # 6042
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 2016
Est. completion date August 2029

Study information

Verified date August 2023
Source University Hospital, Strasbourg, France
Contact Benoît ROMAIN, MD
Phone 03/88/12/72/43
Email benoit.romain@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date August 2029
Est. primary completion date July 2029
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: Gastric adenocarcinoma (any location) or cardia adenocarcinoma - Age> 18 years - WHO Index= 3 - Subject having signed an informed consent Exclusion Criteria: - Other cancers undergoing chemotherapy treatment - Pregnant or breastfeeding - Inability to understand information (understanding with difficulties ...)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Biopsy
Biopsy of Gastric and cardia adenocarcinomas

Locations

Country Name City State
France University Hospital, Strasbourg, france Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of expression level of Met To search in gastric and cardia tumors molecular markers of sensitivity to pre- and post-operative chemotherapy protocols (EOX protocol ... FOLFOX) or chemoradiation at 15 days
Primary Assessment of expression level of Her2 To search in gastric and cardia tumors molecular markers of sensitivity to pre- and post-operative chemotherapy protocols (EOX protocol ... FOLFOX) or chemoradiation at 15 days
Primary Assessment of expression level of FGFR2 To search in gastric and cardia tumors molecular markers of sensitivity to pre- and post-operative chemotherapy protocols (EOX protocol ... FOLFOX) or chemoradiation at 15 days