Circulating tumour DNA assays
Ellery, B, Parsons, J
            Record ID 32018000696
            English
                                                
                Authors' results and conclusions:
                Circulating tumour DNA (ctDNA) assays have the potential to interrogate the cancer genome for specific, pre-selected or unselected abnormalities. This information may then be used for screening, diagnosis, prognosis, in addition to the prediction and monitoring of, the response to therapy. The ability to readily monitor tumour burden and chemo sensitivity has the potential to dramatically alter current clinical practice, in that subclinical responses may be identified early in treatment and chemotherapy adjusted before patients develop an overt relapse. The major advantage of ctDNA assays is that they require a blood sample rather than biopsy sampling using invasive techniques. This is of particular importance for patients in whom biopsy of the primary lesion is impractical or not possible. However, the major disadvantage at this time lies in clarifying the validity of these assays, and their clinical utility when compared with the large extent evidence regarding invasive techniques.
            
                                    
                Authors' recommendations:
                HealthPACT noted that although the sensitivity of this technique is low, it has the potential to reduce the number of invasive biopsies performed, with only patients who test negative needing to undergo biopsy. HealthPACT also noted that circulating tumour DNA assays have the potential to shorten the time from presentation to diagnosis. It is unlikely at this point in time that this technology would be cost-effective once the cost of the technique is taken into account. However, this technology in the future may lead to significant cost-savings and greater patient acceptance as the need to undergo imaging and other diagnostic tests may be reduced. HealthPACT does not support investment in this technology in clinical practice at this time; however it is recommended that the evidence be reviewed again in 24 months.
            
                                    
            Details
                        
                Project Status:
                Completed
            
                                                            
                Year Published:
                2015
            
                                    
                URL for published report:
                Not Available
            
                                                            
                English language abstract:
                An English language summary is available
            
                                    
                Publication Type:
                Not Assigned
            
                                    
                Country:
                Australia
            
                                                
                        MeSH Terms
            - Genetic Markers
- Neoplasms
- Neoplasm Metastasis
- Neoplasm Micrometastasis
- Biomarkers, Tumor
- Circulating Tumor DNA
- Mutation
Keywords
                        - circulating tumour
- DNA
Contact
                        
                Organisation Name:
                Adelaide Health Technology Assessment
            
            
                        
                Contact Address:
                School of Public Health, Mail Drop 545, University of Adelaide, Adelaide SA 5005, AUSTRALIA, Tel: +61 8 8313 4617
            
                                    
                Contact Name:
                ahta@adelaide.edu.au
            
                                    
                Contact Email:
                ahta@adelaide.edu.au
            
                                    
                Copyright:
                Adelaide Health Technology Assessment (AHTA)
            
                    
                This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.