About this trial
As part of the French Genomic Medicine Plan 2025 (FGM), the SeqOIA and AURAGEN platforms were selected to perform high-throughput genomic sequencing.
The SONCO (Sequencing Oncology Cohort) project combines their medical and economic evaluations into a single national cohort. Its objective is to assess the impact of genomic sequencing on care pathways and treatment recommendations by collecting indicators related to quality, turnaround time, and patient information. Clinical data are gathered from molecular tumor board reports (via SPICE and HYGEN) and from hospital medical records.
This cohort is intended to support public health decision-making and help anticipate the organization of future genomic platforms.
Eligibility criteria
Qualifiers
Patients diagnosed with cancer and referred for high-throughput sequencing
Sequencing pre-indication validated: Patients for whom the pre-indication for sequencing the genome, exome, and RNA has been validated by the upstream RCP (Multidisciplinary Tumor Board) since January 1, 2021.
Disqualifiers
Opposition to data reuse, unvalidated upstream RCP
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Assistance Publique - Hôpitaux de Paris
Lead sponsor
AuraGen Aesthetics LLC
Collaborator
Centre Leon Berard
Collaborator
Laboratoire SeqOIA
Collaborator
PLAN FRANCE MÉDECINE GÉNOMIQUE 2025
Collaborator