Clinical and BIOgical Analyses of RECtal Tumors
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Centre Leon Berard
- Enrollment
- 300
- Locations
- 1
- Primary Endpoint
- Establish a correlation between biological data and clinical data of patients with rectal tumors
Study Overview
Brief Summary
Rectal cancer is a common cancer with an incidence of approximately 14,000 new cases per year in France. The survival rate is approximately 50% at 5 years, ranging from 90% for patients with localized rectal cancer to 18% for patients with metastases.
Surgery with local or complete exicion is the standard treatment for early stages. The implementation of Total Neoadjuvant Therapy (TNT) for locally advanced stages has led to a significant improvement in the prognosis for rectal cancer. The complete pathological response rate of aproximately 20% after TNT has led to the "Watch and Wait" strategy, which aims to avoid surgery and preserve the rectum, but there is currently no reliable method for identifying responders. Rectal tumors with mismatch repair defiency (MMRd) and/or High microsatellite instability (MSI-H) are considered resistant to neoadjuvant chemotherapy, but those patients can benefit from immunotherapy treatment. Identifying patients who will respond to immunotherapy is crucial for this type of treatment. Pre-existing immune infiltration within the tumor microenvironnement prior to any treatment is an important prognostic factor and could help predict response to immunotherapy, as well as neoadjuvant treatment. Studying the immune microenvironnement and how it changes during different treatments could therefore help identify responders for whom treatment without surgery could be considered in order to avoid the deterioration in quality of life often associated with this procedure in this type of cancer. Finally, analysis of residual tumor cells after chemotherapy and/or chemoradiotherapy could help identify possible mechanisms of resistance to current treatments and develop strategies to counter them.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Other
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Male or female aged 18 or over
- •Patients who have undergone surgery for rectal cancer since January 1st, 2019
- •Histological diagnosis of rectal adenocarcinoma confirmed on a surgical sample
Exclusion Criteria
- •Not applicable
Arms & Interventions
Adult patient with rectal cancer undergoing surgery at Centre Léon Bérard from 2019
Intervention: Blood sample collection (Procedure)
Adult patient with rectal cancer undergoing surgery at Centre Léon Bérard from 2019
Intervention: Tumor Samples (Procedure)
Adult patient with rectal cancer undergoing surgery at Centre Léon Bérard from 2019
Intervention: Healthy tissue sample (Procedure)
Outcomes
Primary Outcomes
Establish a correlation between biological data and clinical data of patients with rectal tumors
Time Frame: Until up to 3 years follow-up of the last patient enrolled
Secondary Outcomes
- Comparison of stroma of tumor samples from : 1) primary tumors operated after preoperative chemotherapy, 2) biopsies performed before chemotherapy and 3) primary tumors operated without preoperative treatment(Until up to 3 years follow-up of the last patient enrolled)
- Comparision of healthy tissue, stroma of primary tumors samples and metastases in patients for whom samples of primary tumor and metastases will be available.(Until up to 3 years follow-up of the last patient enrolled)