Clinical Trial

A Trial Using Transcriptomic Signatures to Personalize Neoadjuvant Chemotherapy (NAC) for Patients With Resectable Borderline Pancreatic Adenocarcinoma (PDAC)

Study acronym: PRODIGE 104 B
Not Yet Recruiting
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Summary
Pancreatic cancer exhibits significant heterogeneity, which poses a major challenge in selecting the best treatment for patients from the very beginning of care. Modern oncology recognizes the use of companion biomarkers to guide targeted therapy or immune checkpoint inhibitors. However, with regard to chemotherapy-which has long been the cornerstone of cancer treatment and remains crucial for most cancers-few predictive tests are available to guide the choice between monotherapy and combination chemotherapy. Patients included in the PRODIGE 104 B - NEOPREDICT study will be those for whom the GEM transcriptomic signature is negative. This population will be treated according to the standard strategy and will be followed clinically and biologically to describe and identify the characteristics specific to this subgroup, and to compare the usual prognostic factors of this population with those of the GEM-positive population included in the parallel PRODIGE 104 A - NEOPREDICT study
Trial Details
NCT Number NCT07592819
Lead Sponsor Institut Paoli-Calmettes
Collaborators: Federation Francophone de Cancerologie Digestive
Conditions Pancreas Adenocarcinoma (MSI-H), Pancreatic Cancer Resectable
Enrollment 367 participants
Start Date 2026-05
Primary Completion 2030-05 (estimated)
Study Completion 2031-11 (estimated)
Updated on ClinicalTrials.gov 2026-05-18