Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| INSERM U1194, Institut de Recherche en Cancérologie de Montpellier, Campus Val d'Aurelle, 34298 Montpellier cedex 5 | UNKNOWN |
Not provided
Not provided
Not provided
Not provided
Not provided
Upper Urinary Tract Urothelial Carcinomas are rare, aggressive tumors, accounting for 5 to 10% of all urothelial tumors. These include tumors which develop in the renal cavities (renal pelvis, calices) and ureteral tumors. Nephro-ureterectomy is the standard treatment but 80% of patients will have a relapse within 2 years. Only one trial has (Birtle et al. 2020), has shown the interest of postoperative chemotherapy. Neoadjuvant systemic treatment seems particularly interesting for a population which is going to undergo a nephronic loss and therefore reduction in kidney function which is likely to make patients ineligible for cisplatin. In favor of additional immunotherapy, it has been described that upper excretory tract tumors have a high immunogenic potential with a high rate of microsatellite instability.
From surgical samples of patient tumors obtained after nephroureterectomy or biopsy material collected before treatment, we are going to generate patient-derived cell lines and xenograft models in the mouse. A recent publication has demonstrated the feasibility of this approach by specifying that the capture rate of tumor cells is 50% for patient-derived xenografts and 25% for patient-derived cells (Coleman et al. 2020). As tumors harvested from biopsies do not grow in patient-derived xenografts,we plan to graft the biopsies onto chorioallantoic chicken embryo membranes, a model which has never been used for this indication and which is one of the original features of our approach. These three concomitant approaches will allow us to increase our chances of obtaining stable upper urinary tract urothelial carcinoma lines to be used for the screening and identification of new treatments or new combinations of molecules that would benefit patients with upper urinary tract urothelial carcinomas, knowing that very few studies dedicated to this type of cancer have been conducted or published due to the rarity of the disease and the lack of existing models published on the subject of these particular tumors.
.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Measure | Description | Time Frame |
|---|---|---|
| Histological characteristics of patient-derived xenograft models after staining. | Microscopic observation of cells after staining with hematoxylin and eosin | 1-6 months after harvesting |
| Study of genomes of tumor specimens | Exome sequencing of DNA cells isolated from original patient tumor specimens. | 1-6 months after harvesting |
| Alterations in the genomes of patient-derived xenograft tumor models | Exome sequencing of DNA cells isolated from patient-derived xenograft tumor models. | 1-6 months after harvesting |
| Alterations in the genomes of patient-derived cell line models | Exome sequencing of DNA cells isolated from patient-derived cell line models. | 1-6 months after harvesting |
| Study of the transcriptome of patient tumor specimens. | RNA-sequencing of cells isolated from patient tumor specimens. | 1-6 months after harvesting |
| Transcriptome of the patient-derived xenograft tumor models. | RNA-sequencing of cells isolated from patient-derived xenograft tumor models. | 1-6 months after harvesting |
| Transcriptome of the patient-derived cell line models. | RNA-sequencing of cells isolated from patient-derived cell line models. | 1-6 months after harvesting |
| Measure | Description | Time Frame |
|---|---|---|
| Sensitivity to Cisplatin: patient-derived cell line models | The MIC 50 test (Minimum Inhibitory Concentration required for cell growth to be inhibited by 50%) will be used in vitro to test the tumor cells' response to Cisplatin. | 6-8 months after harvesting |
| Sensitivity to Carboplatin: patient-derived cell line models |
| Measure | Description | Time Frame |
|---|---|---|
| Patients' gender | The sex of patients will be recorded at the inclusion as Male/Female/Transgender | Day 0 |
| Patients' age | The age of patients will be recorded at the inclusion in years |
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
The study population consists of patients treated consecutively at the Urology Andrology department of Nîmes University Hospital for high-grade carcinomas of the pelvis or renal ureter for whom a total nephroureterectomy has been indicated during a multidisciplinary meeting. The tumor samples used for our study come from specimens removed surgically. Patients must not have undergone any prior systemic treatment.
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Nadine HOUEDE, Pr. | CHU de Nimes | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre Hospitalier Universitaire de Nîmes | Nîmes | Gard | 30029 | France |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 32145825 | Background | Birtle A, Johnson M, Chester J, Jones R, Dolling D, Bryan RT, Harris C, Winterbottom A, Blacker A, Catto JWF, Chakraborti P, Donovan JL, Elliott PA, French A, Jagdev S, Jenkins B, Keeley FX Jr, Kockelbergh R, Powles T, Wagstaff J, Wilson C, Todd R, Lewis R, Hall E. Adjuvant chemotherapy in upper tract urothelial carcinoma (the POUT trial): a phase 3, open-label, randomised controlled trial. Lancet. 2020 Apr 18;395(10232):1268-1277. doi: 10.1016/S0140-6736(20)30415-3. Epub 2020 Mar 5. |
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D009369 | Neoplasms |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Tumor samples removed by nephroureterctomy will be evaluated at Nîmes University Hospital's Pathological Anatomy and Cytology Department. Part of the tumors are dissected into 2-3 mm3 fragments and quickly transported in cold Roswell Park Memorial Institute medium or a phosphate-buffered saline environment to the animal lab for subcutaneous grafting on mice or to the "Resistance to innovative treatments and therapies" team for soft cell dissociation. Cell suspensions will then be transported on ice to our collaborators at Inovotion Laboratories for grafting into the chorioallantoid membrane of chicken embryos, or used for cold in vitro culture at the animal lab for subcutaneous grafts (patient-derived xenograft models).
The MIC 50 test (Minimum Inhibitory Concentration required for cell growth to be inhibited by 50%) will be used in vitro to test the tumor cells' response to Carboplatin. |
| 6-8 months after harvesting |
| Sensitivity to Oxaliplatin: patient-derived cell line models | The MIC 50 test (Minimum Inhibitory Concentration required for cell growth to be inhibited by 50%) will be used in vitro to test the tumor cells' response to Oxaliplatin. | 6-8 months after harvesting |
| Sensitivity to Gemcitabin: patient-derived cell line models | The MIC 50 test (Minimum Inhibitory Concentration required for cell growth to be inhibited by 50%) will be used in vitro to test the tumor cells' response to Gemcitabin. | 6-8 months after harvesting |
| Tumor size in non-treated patient-derived xenograft models | The volume of tumors will be measured in mm3. | 1-6 months after harvesting |
| Sensitivity to Cisplatin: tumor size in treated patient-derived xenograft models | To test the tumor cells' response to Cisplatin in xenograft models, the volume of tumors will be measured in mm3 and compared with the volume of tumors in the non-treated control group. | 6-8 months after harvesting |
| Sensitivity to Cisplatin: tumor growth rate in patient-derived xenograft models | To test the tumor cells' response to Cisplatin in xenograft models, the Tumor Growth Inhibition index, which is defined as (1 - (mean volume of treated tumors)/(mean volume of control tumors)) × 100% will be used. | 6-8 months after harvesting |
| Sensitivity to Carboplatin: tumor size in treated patient-derived xenograft models | To test the tumor cells' response to Carboplatin in xenograft models, the volume of tumors will be measured in mm3 and compared with the volume of tumors in the non-treated control group. | 6-8 months after harvesting |
| Sensitivity to Carboplatin: tumor growth rate in treated patient-derived xenograft models | To test the tumor cells' response to Carboplatin in xenograft models, the Tumor Growth Inhibition index, which is defined as (1 - (mean volume of treated tumors)/(mean volume of control tumors)) × 100% will be used. | 6-8 months after harvesting |
| Sensitivity to Oxiplatin: tumor size in treated patient-derived xenograft models | To test the tumor cells' response to Oxiplatin in xenograft models, the volume of tumors will be measured in mm and compared with the volume of tumors in the non-treated control group. | 6-8 months after harvesting |
| Sensitivity to Oxiplatin: tumor growth rate in treated patient-derived xenograft models | To test the tumor cells' response to Oxiplatin in xenograft models, the Tumor Growth Inhibition index, which is defined as (1 - (mean volume of treated tumors)/(mean volume of control tumors)) × 100% will be used. | 6-8 months after harvesting |
| Sensitivity to Gemcitabine: tumor size in treated patient-derived xenograft models | To test the tumor cells' response to Gemcitabine in xenograft models, the tumor volume will be measured in mm3 and compared with the volume of tumors in the non-treated control group. | 6-8 months after harvesting |
| Sensitivity to Gemcitabin: tumor growth rate in treated patient-derived xenograft models | To test the tumor cells' response to Gemcitabin in xenograft models, the Tumor Growth Inhibition index, which is defined as (1 - (mean volume of treated tumors)/(mean volume of control tumors)) × 100% will be used. | 6-8 months after harvesting |
| Day 0 |
| Primitive tumor site | The site of the patient's primitive tumor will be recorded at the inclusion | Day 0 |
| Infiltrative tumor | The tumor will be noted as infiltrative or not (YES/NO) at the inclusion. | Day 0 |