Actively Recruiting

Age: 18Years +
All Genders
ID06160596

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

Led by Cure 51 · Updated on 2023-12-07

1020

Participants Needed

1

Research Sites

130 weeks

Total Duration

On this page

Sponsors

C

Cure 51

Lead Sponsor

G

Gustave Roussy, Cancer Campus, Grand Paris

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a retrospective, exploratory study involving three groups of patients who have solid tumors with poor prognosis but show either long-term or standard survival. The study focuses on metastatic pancreatic ductal adenocarcinoma, glioblastoma IDH wild-type, and extensive small cell lung cancer. The goal is to integrate data from clinical records, imaging, and multiple omics technologies to identify differences between patients with exceptional survival and those with typical outcomes, aiming to find new therapeutic targets. The study collects biological samples and clinical information from patients who survived longer than usual—over 5 years for pancreatic and small cell lung cancer, and over 3 years for glioblastoma. Data from multiple molecular levels including genomic, epigenomic, proteomic, metabolomic, transcriptomic, and microbiomic analyses will be combined and analyzed using advanced bioinformatics and artificial intelligence techniques. Researchers will compare these findings with control patients who had standard survival times. Participants' tumor samples and clinical data will be centralized and analyzed to identify molecular signatures associated with long-term survival. The study uses digital histology, radiomics, and multi-omics to characterize these signatures within each cancer cohort and across all groups. The primary outcome is measuring exceptional survival at 54 months. This observational study involves no treatment interventions, focusing instead on data collection and analysis to improve understanding of cancer resistance and survival.

CONDITIONS

Brief Title

Analyzing and Solving Exceptional Long-term Survivors in Solid Tumors With Poor Prognosis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients aged 18 years or older at diagnosis
  • Diagnosis of metastatic pancreatic ductal adenocarcinoma, glioblastoma IDH wild-type, or extensive small cell lung cancer
  • Long-term survival defined as at least 5 years from stage IV diagnosis for pancreatic and small cell lung cancer, and at least 3 years for glioblastoma
  • Availability of at least one tumor block sample of sufficient quality and quantity for multi-omic analyses
  • Samples must be at least 5 years old for pancreatic and small cell lung cancer, and 3 years old for glioblastoma
  • Control patients matched to long-term survivors with death or median overall survival within 10% variation from clinical trial reports
  • Treatment history reported prior to sample acquisition; all treatments accepted (standard or targeted)
Not Eligible

You will not qualify if you...

  • Patients younger than 18 years at diagnosis
  • Diagnosis of hematological malignancies or solid tumors outside the specified tumor types
  • Tumor samples unavailable or not meeting quality requirements for multi-omic analyses

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surveillance

Duration - Ongoing throughout the study duration

Participants who meet eligibility criteria have their biological samples and clinical records collected and centralized to analyze molecular signatures associated with long-term survival in solid tumors.

Trial Site Locations

Total: 1 location

1

Gustave Roussy Cancer Campus, Grand Paris

Villejuif, France, 94805

Actively Recruiting

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Research Team

W

Wolikow Nicolas, Master

S

Simon Istolainen, Master

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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