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Active, not recruiting Not applicable

Personalized First-line Chemotherapy Choice in Advanced Pancreatic Adenocarcinoma Using Transcriptomic Signatures

NCT05475366 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2022-12-12
Last updated
2026-10-01

Condition(s) studied

Carcinoma, Pancreatic DuctalPrognosis

Investigational drug(s) / intervention(s)

Clinical value of 5 transcriptomic signatures to personalize the therapeutic decision for L1 in PDACBiomarkers of tumor signatures (translational studies)

Clinical value of 5 transcriptomic signatures to personalize the therapeutic decision for L1 in PDAC: Formalin-Fixed Paraffin-Embedded (FFPE) samples will be centralized in which nucleic acids extraction (DNA+RNA) and FFPE-compatible RNA-sequencing will be performed in real-time (≤28 days). RNAseq reads will be processed and all 5 transcriptomic signatures will be applied for prediction of response to 5FU, oxaliplatin, irinotecan, gemcitabine and taxane. In addition, biomarkers status will be obtained for all patients as part of good clinical practice.

Biomarkers of tumor signatures (translational studies): Blood (serum and plasma) will be drawn at baseline, week 8, and tumor progression in order to look for surrogate biomarkers of tumor signatures in liquid biopsy

Study summary

The aim of this study is to assess the clinical value of 5 transcriptomic signatures prognostic of chemotherapeutic sensitivity to improve the Objective Response Rate (ORR) of first-line (L1). Chemotherapy regimen (FOLFIRINOX vs Gem-nabP) will be selected based on transcriptomic signatures applied to the pre-therapeutic liver biopsy of newly diagnosed PDAC patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: 1. Written informed consent obtained from the patient prior to performing any protocol-related procedures, including screening evaluations. 2. Willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up. 3. Histologically or cytologically proven Pancreatic Ductal Adenocarcinoma (PDAC). 4. Metastatic disease. 5. Measurable or evaluable lesions according to RECIST v1.1 criteria. 6. First-line therapy (previous neoadjuvant/adjuvant chemotherapy not allowed). 7. Age ≥ 18 years (no upper limit, patients ≥ 75 years old must have a G8 score ≥ 14). 8. 3\. Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0-1. 9. Availability of tumor tissue sample from the primary pancreatic tumor or liver metastasis (chemo-naïve) before inclusion in step 1. 10. Adequate organ function, as defined by the following (blood test ≤ 7 days prior to inclusion): 1. Serum aspartate aminotransferase (AST) and serum alanine aminotransferase (ALT) ≤ 3 x upper limit of normal (ULN) (≤ 5 ULN in case of liver metastases) 2. Total serum bilirubin ≤ 1.5 ULN 3. Serum albumin ≥ 28 g/L 4. Hemoglobin ≥ 9.0 g/dl 5. Absolute neutrophil count (ANC) ≥ 1,500/μL 6. Platelets ≥ 100,000/μL 7. Creatinine clearance ≥ 50 mL/min (MDRD). 11. No Dihydropyrimidine dehydrogenase (DPD) deficiency (normal uracil level). 12. Life expectancy ≥ 3 months. 13. a. Evidence of post-menopausal status b. (or) negative urinary or serum pregnancy test for female pre-menopausal patients. 14. Registration in a National Health Care System. Exclusion Criteria: 1. Concurrent enrolment in another interventional clinical study. 2. Previous treatment with chemotherapy for pancreatic cancer. 3. Uncontrolled massive pleural effusion or massive ascites. 4. Known deficiency in UGT1A1 (homozygous UGT1A1\*28 allele). 5. Active bacterial, viral, or fungal infection requiring systemic therapy, including tuberculosis, hepatitis B (known positive Hepatitis B Virus surface antigen (HBsAg) result), hepatitis C (with positive RNA), Sars-Cov-2 or human immunodeficiency virus (positive HIV 1/2 antibodies). 6. Diagnosis of any second malignancy within the last 3 years, except for adequately treated basal cell or squamous cell skin cancer, or in situ carcinoma of the cervix uteri. 7. Known active central nervous system metastases and/or carcinomatous meningitis; patients with previously treated brain metastases may participate provided they are stable (without evidence of progression by imaging for at least 4 weeks prior to the first dose of trial treatment and any neurologic symptoms have returned to baseline). 8. Uncontrolled intercurrent illness, including but not limited to, symptomatic congestive heart failure or coronary disease, peripheral artery disease, severe chronic obstructive pulmonary disease, decompensated cirrhosis, serious chronic gastrointestinal conditions associated with diarrhea, or psychiatric illness/social situations that would limit compliance with study requirement, substantially increase risk of incurring AEs or compromise the ability of the patient to give written informed consent. 9. Live vaccine administration within 30 days prior to the first dose of study treatment. 10. Known or suspected allergy or hypersensitivity to any of the study drugs or any of the study drug excipients. 11. History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with participation for the full duration of the trial, or is not in the best interest of the participant, in the opinion of the treating investigator. 12. Radiotherapy treatment to more than 30% of the bone marrow or with a wide field of radiation within 4 weeks of the first dose of study drug. 13. Major surgical procedure (as defined by the Investigator) within 4 weeks prior to the first dose of trial treatment. 14. Pregnancy/lactation. 15. Person under legal protection or tutelage or guardianship.

Primary outcome measure(s)

  • Objective Response Rate (ORR) at 4 months based on thorax-abdomen-pelvis (TAP) CT scan every 8 weeks according to RECIST v1.1. — 4 months
    ORR, defined as the percentage of patients whose disease decreased by at least 30% (partial response - PR) and/or disappeared (complete response - CR) under treatment among patients who start treatment.

Trial sites (7)

FacilityCityRegionStatus
Hôpital Beaujon Clichy France
Hôpital HENRI MONDOR Créteil France
Hôpital Claude Hurriez Lille France
Institut Paoli-Calmettes Marseille France
CHU Robert Debré Reims France
Institut Curie Saint-Cloud France
Hôpital PAUL BROUSSE 12 Avenue Paul Vaillant Couturier Villejuif France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05475366 on ClinicalTrials.gov ↗ ← All trials in France