Copenhagen Prospective Personalized Oncology (CoPPO) — CoPPO  

Unspecified Adult Solid Tumor, Protocol Specific Clinical Trial

Official title: A Prospective Study Using Genomic Screening to Select Patients for Targeted Molecular Treatment

Status Recruiting

Clinical Trial Summary

Patients with advanced solid tumors referred to the Phase 1 Unit are offered mapping of GA for identification of pts who could benefit from a personalized treatment.

Clinical Trial Description

Two ultrasound-guided biopsies obtained to be stored in RNAlater® for DNA and RNA purification. A 3rd biopsy for histology is paraffin embedded. SNP-array (Affymetrix Cytoscan HD) from DNA (tumor) is performed to identify copy number changes. Whole exome sequencing (WES) from DNA (tumor and blood) will be performed using sequence capture, SureSelect v5 (Agilent) and Illumina HiSeq2500 to call tumor specific mutations. Expression levels of therapeutic targets are revealed by expression Array from tumor RNA. In addition to the expression array, RNA-seq (Nugens Ovation RNA-seq system v2) is performed to investigate whether chromosomal translocations were the reason for tumor specific expression of an oncogene. Results will be reviewed by a tumor board. Patients with specific genetic profiles that can be targeted with marketed drugs or drugs under development are offered such treatment. PFS from the treatment is compared to PFS of the most recent standard treatment (PFS ratio). ;

Related Conditions & MeSH terms

• Unspecified Adult Solid Tumor, Protocol Specific

• NCT number: NCT02290522
• Study type: Interventional
• Source: Rigshospitalet, Denmark
• Contact: Ida V Tuxen, MD
• Phone: +4535453545
• Status: Recruiting
• Phase: N/A
• Start date: May 2013
• Completion date: December 2023