Skip to main content
Clinical Trials/NCT02301858
NCT02301858
Active, Not Recruiting
N/A

Identification of Predictive and Prognostic Markers for Lung Cancer With Metastases

Janna Berg1 site in 1 country100 target enrollmentDecember 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
Lung Cancer
Sponsor
Janna Berg
Enrollment
100
Locations
1
Primary Endpoint
Comparing histopathological and molecular characteristics of tumour tissue from metastases with the primary tumour in the lung
Status
Active, Not Recruiting
Last Updated
3 years ago

Overview

Brief Summary

The project aims to compare the histopathological and molecular characteristics of tumour tissue from metastases with similar analyses of the primary tumour in the lung, where it is available.

The investigators will therefore perform analysis of blood samples if possible, to identify predictive markers in blood samples.

Detailed Description

The investigators want to make genome analysis of tissue samples. This involves analysing the RNA, DNA methylation, for example in cancer cells. This will provide information regarding somatic changes in cancer cells, such as mutations. All of the investigators analysis will be cancer-focused, with the goal of increasing understanding of the heterogeneity. The investigators will therefore perform analysis of blood samples if possible, to identify predictive markers in blood samples. This will then be the miRNA, RNA expression or protein expression in blood samples.

Registry
clinicaltrials.gov
Start Date
December 2013
End Date
December 2025
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Janna Berg
Responsible Party
Sponsor Investigator
Principal Investigator

Janna Berg

Consultant

Sykehuset i Vestfold HF

Eligibility Criteria

Inclusion Criteria

  • Patients with metastasizing lung cancer where further treatment is still applicable.

Exclusion Criteria

  • Terminal patients or patients in a reduced general condition with EGOC 3-4, i.e. patients who are confined to bed more than 50% of the day, with no clinical indication to perform sampling of the tumor and metastases.
  • Patients where further cancer treatment is no longer applicable.
  • Patients with cognitive impairment.
  • Patients with inaccessible metastases where sampling may cause distress to the patient and are at increased risk of complications.

Outcomes

Primary Outcomes

Comparing histopathological and molecular characteristics of tumour tissue from metastases with the primary tumour in the lung

Time Frame: 5 years

We will do profiling of the mRNA (messenger ribonucleic acid) expression of microRNA and perform single nucleotide polymorphism analysis of cancer tissue and compare the expression using statistical methods such as SAM (Significance analysis and microarrays), PAM (Prediction analysis of microarrays). In addition, we wish to perform specific genetic analysis of cancer-related genes. These will be made with available methods like sequencing or TaqMan assays for specific mutations. Blood samples will be analysed by microarray methods for RNA and microRNA in addition to serum analysis of proteins.

Study Sites (1)

Loading locations...

Similar Trials