Analyzing and Solving Exceptional Long-term Survivors in Solid Tumors With Poor Prognosis: A 3 Cohorts Case Control Matched Study

Status: Recruiting
Location: See location...
Intervention Type: Genetic
Study Type: Observational
SUMMARY

This is a retrospective, exploratory, multi-center, translational, 3 cohorts case control matched study conducted in patients harboring a solid tumor with poor prognosis who presented a long-term (case) and standard (standard) survival. Patients with: * Cohort A: metastatic pancreatic ductal adenocarcinoma * Cohort B: glioblastoma IDHwt * Cohort C: extensive small cell lung cancer This research aims to integrate data generated from clinical records, imaging, multi-omics and bioinformatics approaches to discriminate case and control and then to identify new therapeutic targets. Analyses will be performed depending on the tumor samples available with at least 3 omics levels and according to scientific advances; genomic, epigenomic, proteomics, metabolomics, transcriptomic, microbiomic.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ FOR SURVIVORS

• To be eligible the exceptional survivor patients must fulfill the following inclusion criteria:

‣ Adult patient (≥18 years old at diagnosis).

⁃ Three distinct cohorts, one of patients harbouring metastatic pancreatic ductal adenocarcinoma, glioblastoma IDHwt, extensive small cell lung cancer.

⁃ Long-term survival is defined as an exceptionally long survival ≥ 5 years from stage IV diagnosis for PDAC, extensive SCLC, and ≥ 3 years for GBM-IDHwt.

⁃ Availability of at least one block sample and associated clinical annotations with following characteristics:

• One block sample must be of sufficient quality and in sufficient quantity to perform multi-omic analyses, according to requirements specified in Lab manual

∙ Any treatment prior to sample acquisition must be reported - all treatments accepted (standard / targeted);

∙ Samples should be at least 5 years old for PDAC and SCLC and 3 years old for GBM

⁃ For CONTROL GROUPS :

• To be eligible the control patients must fulfill the following inclusion criteria:

‣ ≥18 years old at diagnosis.

⁃ Three distinct cohorts, one of patients suffering from metastatic pancreatic ductal adenocarcinoma, one for glioblastoma, one for extensive small cell lung cancer.

⁃ Paired to long-term survivors as mentioned in the methodology section

⁃ Death or median overall survival with a variation of 10% before of beyond as reported in pivotal clinical trials in the specific type disease

⁃ Availability of at least one tumor sample and associated clinical annotations with following characteristics:

• Sample must be of sufficient quality and in sufficient quantity to perform multi-omic analyses

∙ Any treatment prior to sample acquisition must be reported (treatment-naive samples should be preferred) - all treatments accepted (standard / targeted).

Locations
Other Locations
France
Gustave Roussy Cancer Campus, Grand Paris
RECRUITING
Villejuif
Contact Information
Primary
Wolikow Nicolas, Master
nicolas@cure51.com
0033772042022
Backup
Simon Istolainen, Master
simon@cure51.com
0033626955716
Time Frame
Start Date: 2023-11-01
Estimated Completion Date: 2028-05-01
Participants
Target number of participants: 1020
Treatments
PDAC STAGE IV SURVIVORS & CONTROLS
Metastatic pancreatic ductal adenocarcinoma (PDAC) (Other histologies such as adenosquamous carcinoma, hepatoid carcinoma, anaplastic undifferentiated carcinoma and medullary carcinoma, acinar cell carcinoma, neuroendocrine tumors, Solid pseudopapillary neoplasm, Pancreatoblastoma, Serous cystadenocarcinoma are excluded)
SMALL CELL LUNG CANCER EXTENSIVE STAGE SURVIVORS & CONTROLS
Extensive small cell lung cancer (SCLC) (Other histologies excluded: combined SCLC with some areas of non-small cell lung cancer (NSCLC), carcinoid tumors, typical and atypical, large cell neuroendocrine carcinoma of the lung).
GLIOBLASTOMA SURVIVORS & CONTROLS
Glioblastoma (GBM) (IDH mutated excluded)
Sponsors
Collaborators: Centre Leon Berard, Istituto Europeo di Oncologia, Charite University, Berlin, Germany, Vall d'Hebron Institute of Oncology, Gustave Roussy, Cancer Campus, Grand Paris
Leads: Cure 51

This content was sourced from clinicaltrials.gov