Circulating Tumor Cell, Colo-rectal Cancer, Immune Evasion, Tumor, Neoplastic Cells, Circulating, Pulmonary Metastasis
Conditions
Keywords
Colo-rectal cancer, Lung metastasis, Radiofrequency ablation, Tumor infiltrating lymphocytes, Circulating tumor cells, Circulating DNA
Brief summary
Local percutaneous thermal ablation is frequently proposed in the management of metastatic diseases. Radiofrequency ablation (RFA) has demonstrated good results when the metastatic disease is limited and slowly evolving. The destruction of solid metastasis by RF leads to inflammatory and immunological mechanisms that remain poorly understood. These pathological events may influence the overall and anti-tumor host immune responses. The purpose of the study is to identify and quantify some immune mechanisms triggered by RFA of pulmonary metastases from colorectal cancer origin.
Detailed description
RFA could provide activatory signals and become a source of tumor antigens for the immune system. Generating a massive and transient release of antigens, RFA could boost lymphocyte proliferation and production of inflammatory cytokines in response to tumor extracts. Herein, the investigator aims to demonstrate that RFA can amplify the specific T cell response in metastatic cancer patients. In order to ensure this, he plans to assess and quantify tumor infiltrating lymphocytes through tumoral biopsies. He also plans to measure the CD4, CD8 and NK lymphocytes release, the circulating DNA and tumoral cells release, during RFA of lung metastases. On tumoral biopsies, the expression of PDL-1 ligand will also be evaluated and measured. Participants with bilateral metastases or with 5 or more unilateral metastases will be recruited. The two RFA interventions will be carried out within 4-6 weeks of each other. Blood samples and tumoral biopsies will be performed during each intervention. Biopsies will be performed on a metastasis before the thermal ablation. Blood samples will be performed just before RFA, 30 min after RFA and one day after. Analysis, identification and measure of lymphocytes release will be performed with flow cytometry. All analysis and measurements will be performed in the Bio-Pathology department of Institut Bergonié.
Interventions
RADIATIONRFA interventions
Each patient is treated with 2 RFA interventions. Abiopsy of one metastasis is done at each RF session. Histological samples are sent to the Bio-pathology department of Institut Bergonié for tumor infiltrating lymphocytes counting. Primary outcome results from this counting (stromal TILs ≥ 20% is considered as a significant level, a comparative measurement before and after RF will be performed). In parallel blood samples are performed before and after RFA to analyze the kinetics of peripheral blood T lymphocytes subsets, tumoral circulating cells and tumoral DNA.
Sponsors
Institut Bergonié
Groupement Interrégional de Recherche Clinique et d'Innovation
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Patient older than 18 years-old. 2. OMS performance status ≤ 2. 3. Colorectal cancer histologically established previously. 4. Primary tumor resected. 5. Lung metastasis: 1. Bilateral metastasis (or unilateral metastases that need to undergo the RF in two separate sessions due to the number of metastases ≥ 5) 2. Maximal diameter ≤ 4 cm, 3. non or slowly progressive, with or without chemotherapy, 4. eligible to RFA. 6. Thorax-abdomen-pelvis CT scan and PET scan: 1. performed within 8 weeks before inclusion 2. finding no more than 10 metastatic nodules (liver + lung or lung alone) 7. Maximum of 8 weeks between the last cycle of chemotherapy and the first RFA. 8. Decision of local treatment agreed at the multidisciplinary digestive tumor board. 9. Life expectancy ≥ 3 months. 10. Voluntarily signed and dated written informed consent prior to any study specific procedure. 11. Patients with a French social security in compliance with the Law relating to biomedical research (Article 1121-11 of French Public Health Code).
Exclusion criteria
1. Other than lung or liver metastases. 2. Contraindication to general anesthesia. 3. Contraindication to RFA: tumor location (\< 1cm from the hilum), lung insufficiency (FEV/sec \< 1l), 4. Pregnant or lactating women. 5. Concomitant participation to another interventional research. 6. Patient unable to follow and comply with the study procedures because of any geographical, social or psychological reasons. 7. Patient deprived of liberty or under legal protection measure.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Immune Response Triggered by RFA: Change From Rate of Tumor Infiltrating T Lymphocytes on Tumoral Stroma Measured Before and After RFA1. | Day 1 |
| Immune Response Triggered by RFA: Change From Rate of Tumor Infiltrating T Lymphocytes on Tumoral Stroma Measured Before and After RFA2. | Week 6 |
| Immune Response Triggered by RFA: Quantification of Interaction of PD-1 and PD-L1 in Lung Metastases Using Immune Förster Resonance Energy Transfer (iFRET). | Day 1 |
Countries
France
Contacts
PRINCIPAL_INVESTIGATORJean PALUSSIERE, MD
Institut Bergonié
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Single arm Each patient is treated with 2 RFA interventions.
RFA interventions: Each patient is treated with 2 RFA interventions. Abiopsy of one metastasis is done at each RF session. Histological samples are sent to the Bio-pathology department of Institut Bergonié for tumor infiltrating lymphocytes counting. Primary outcome results from this counting (stromal TILs ≥ 20% is considered as a significant level, a comparative measurement before and after RF will be performed). In parallel blood samples are performed before and after RFA to analyze the kinetics of peripheral blood T lymphocytes subsets, tumoral circulating cells and tumoral DNA. | 17 |
| Total | 17 |
Baseline characteristics
| Characteristic | Single arm |
|---|---|
| Age, Continuous | 70.8 years |
| Region of Enrollment France | 17 participants |
| Sex: Female, Male Female | 6 Participants |
| Sex: Female, Male Male | 11 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | 0 / 20 |
| other Total, other adverse events | 19 / 20 |
| serious Total, serious adverse events | 0 / 20 |
Outcome results
Primary
Immune Response Triggered by RFA: Change From Rate of Tumor Infiltrating T Lymphocytes on Tumoral Stroma Measured Before and After RFA1.
Time frame: Day 1
Population: Biological analyses could not be performed (technical reasons related to the machine). As such, it was not possible to assess this outcome and report summary statistics as expected.~No attempt will be made in the future to collect and/or report the data
Primary
Immune Response Triggered by RFA: Change From Rate of Tumor Infiltrating T Lymphocytes on Tumoral Stroma Measured Before and After RFA2.
Time frame: Week 6
Population: Biological analyses could not be performed (technical reasons related to the machine). As such, it was not possible to assess this outcome and report summary statistics as expected.~No attempt will be made in the future to collect and/or report the data
Primary
Immune Response Triggered by RFA: Quantification of Interaction of PD-1 and PD-L1 in Lung Metastases Using Immune Förster Resonance Energy Transfer (iFRET).
Time frame: Day 1
Population: Biological analyses could not be performed (technical reasons related to the machine). As such, it was not possible to assess this outcome and report summary statistics as expected.~No attempt will be made in the future to collect and/or report the data
Primary
Immune Response Triggered by RFA: Quantification of Interaction of PD-1 and PD-L1 in Lung Metastases Using Immune Förster Resonance Energy Transfer (iFRET).
Time frame: Week 6
Population: Biological analyses could not be performed (technical reasons related to the machine). As such, it was not possible to assess this outcome and report summary statistics as expected.~No attempt will be made in the future to collect and/or report the data