Performance Indicators and Impact on the Care Pathway of Sequencing on the SeqOIA and AURAGEN (Seqogen) Platforms for Oncology Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorAssistance Publique - Hôpitaux de Paris

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

No trial groups listed

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