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The goal of this retrospective study is to identify predictive biomarkers of efficacy in tumor samples of small cell lung cancer patients treated with chemotherapy-immunotherapy combination using imaging mass cytometry. The main question it aims to answer is: is there any feature in the tumour microenvironment that can discriminate responders from non responders before treatment? Participants will provide consent for the collection of their clinical data and the study of their tumor samples
Small cell lung cancer patients treated with first-line atezolizumab plus platinum-etoposide regimen with available formalin fixed paraffin embedded (FFPE) biopsies at baseline will be identified from Brest University Hospital medical records and their samples will be retrieved from Brest University Hospital Pathology Laboratory for imaging mass cytometry analyses.
Clinical data will be collected for each patient, including progression-free survival (defined as the time between treatment start and date of progression according to investigator, or death from any cause) and overall survival (defined as the time between treatment start and date of death from any cause).
For imaging mass cytometry analyses, a panel of 39 metal-tagged antibodies will be used to characterize the cell composition of lung tumors at baseline (inflammatory, tumor and stromal cells).
Statistical analyses will be performed to correlate the composition of the tumor microenvironment at baseline and the survival data.
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| Measure | Description | Time Frame |
|---|---|---|
| Identification of predictive biomarkers of anti-PD-L1 efficacy in the tumor of small cell lung cancer patients | Features in the tumour microenvironment that can discriminate patients responding to anti-PD-L1 from non responders | 3 year |
| Measure | Description | Time Frame |
|---|---|---|
| Progression-free survival | Time between treatment start and date of progression according to investigator, or death from any cause | 3 year |
| Overall survival | Time between treatment start and date of death from any cause |
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Inclusion Criteria:
Exclusion Criteria:
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All patients who started a first line treatment with atezolizumab plus carboplatin and etoposide at Brest University Hospital before February 2021 with available tumor sample before treatment start
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| Name | Affiliation | Role |
|---|---|---|
| Margaux Geier, MD | Department of Medical Oncology, Brest University Hospital | Study Director |
| Pierre Le Noac'h, MD | Department of Medical Oncology, Brest University Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU de Brest | Brest | 29609 | France |
All collected data that underlie results in a publication
Data will be available after the publication of result and ending five years maximum following the last visit of the last patient
Data access requests will be reviewed by the internal committee of Brest University Hospital. requestors will be required to sign and complete a data access agreement
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Fixed tissue
| 3 year |
| ID | Term |
|---|---|
| D055752 | Small Cell Lung Carcinoma |
| ID | Term |
|---|---|
| D002283 | Carcinoma, Bronchogenic |
| D001984 | Bronchial Neoplasms |
| D008175 | Lung Neoplasms |
| D012142 | Respiratory Tract Neoplasms |
| D013899 | Thoracic Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
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