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Our goal is to create novel CD47-SIRPα inhibitors using small molecules to reverse TAM-mediated immune suppression and restore anti-tumor immunity in CRCs. Our program uses structure-based drug design to create selective and potent small molecule inhibitors of SIRPα-CD47 to target the tumor microenvironment with greater efficacy and lower toxicity than CD47-targeting antibodies. .
In order to study the activity of CD47-SIRPα inhibitors on the immune microenvironment of tumors, we propose to use organoids derived from biopsies of patients with colon cancer. Tumoroids preserve the patient's tumor stroma (including myeloid cells) and provide an accurate in vitro model of complex tumor immune interaction for the evaluation of immunotherapies.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| BLOOD AND TUMOR | Procedure | sampling of 24 ml of peripheral blood and samples of colon cancers with healthy tissue in parallel on the surgery piece |
| Measure | Description | Time Frame |
|---|---|---|
| Establishment of patient derived organoids (minimum n=30) resembling the primary tissue sample | the capacity to establish patient-derived organoids from tumor and adjacent normal tissue will be evaluated using a histology score evaluating and comparing primary and organoid sample characteristics. | 18 months from study launch |
| Measure | Description | Time Frame |
|---|---|---|
| Establishment of a validated cryobank of patient derived organoids (minimum n=30) | the capacity to establish a cryobank of patient-derived organoids from tumor and adjacent normal tissue will be evaluated using a growth score evaluating and comparing organoid sample characteristics pre- and post-cryopreservation and amplification through 4 passages. | 18 months from study launch |
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Inclusion Criteria:
Exclusion Criteria:
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The population studied concerns patients over the age of 18, suffering from colon cancer, undergoing immediate surgery or after chemotherapy.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Dominique GENRE, MD | Contact | +33491223778 | drci.up@ipc.unicancer.fr |
| Name | Affiliation | Role |
|---|---|---|
| Cécile de CHAISEMARTIN, MD | Paoli Calmettes Institute | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Institut Paoli Calmettes | Recruiting | Marseille | 13009 | France |
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| ID | Term |
|---|---|
| D003110 | Colonic Neoplasms |
| ID | Term |
|---|---|
| D015179 | Colorectal Neoplasms |
| D007414 | Intestinal Neoplasms |
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
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| ID | Term |
|---|---|
| D047368 | Tumor Burden |
| ID | Term |
|---|---|
| D001837 | Body Weights and Measures |
| D000886 | Anthropometry |
| D008919 | Investigative Techniques |
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peripheral blood; samples of colon cancers with healthy tissue in parallel on the surgical specimen
| Generate a T cell biobank by FACS isolating T cells using the CD3 surface marker directed against the human form | 48 month |
| To assess the effect of immunotherapy on the antitumor activity of autologous T cells from peripheral blood samples using tumor viability measurements (cell titer glo, FACS) | 48 month |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D004066 | Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |