Carcinoma, Pancreatic Ductal, Prognosis
Conditions
Keywords
Transcriptomic signatures, Personalized first-line chemotherapy, Metastatic PDAC
Brief 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.
Detailed description
Step 1: patients will sign a 1st informed consent prospectively for the molecular screening (RNAseq profile). 5 transcriptomic signatures will be applied for prediction of response to 5 Fluoro-Uracil (5FU), oxaliplatin, irinotecan, gemcitabine and taxane. Biomarker status will be obtained for all patients as part of good clinical practice. Patients will be eligible for prospective step 2 only if the transcriptomic analysis is informative and the treatment can be started within 28 days. Step 2: study treatment strategy: based on the results of transcriptomic signatures, patients will receive either FOLFIRINOX or Gem-nabP according to the following algorithm (2nd informed consent): * Predicted to be FOLFIRINOX sensitive (regardless of sensitivity to Gem-nabP) = FOLFIRINOX * Predicted to be FOLFIRINOX and Gem-nabP resistant = FOLFIRINOX * Presence of a germline breast cancer (BRCA) mutation (regardless of transcriptomic signature) = FOLFIRINOX (tumors sensitive to platinum). * Predicted to be Gem-nabP sensitive and FOLFIRINOX resistant = Gem-nabP Chemotherapy with FOLFIRINOX and Gemcitabine plus nab-paclitaxel will be administered as in routine practice, according to their approval. Dose adaptation will be allowed according to investigator's usual practice.
Interventions
OTHERClinical 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.
OTHERBiomarkers 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
Sponsors
Institut Curie
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 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. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Progression-Free Survival (PFS) | 18 months | PFS, defined as the time from the date of treatment initiation to the date of progression or death whatever the cause. Progression will be assessed by the investigator based on TAP-CT scan every 8 weeks according to RECIST v1.1. |
| Overall Survival (OS) | 18 months | OS, defined from the date of treatment initiation to the date of death whatever the cause. |
| Disease Control Rate (DCR) | 18 months | DCR, defined as the percentage of patients who have achieved complete response, partial response or stable disease according to RECIST v1.1 among patients who start treatment. |
| Treatment-related severe (grade 3-5) toxicities | 18 months | Toxicities will be graded, according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v5.0 (digestive, hematologic, neuropathy). |
| Feasibility of study procedure | 12 months | Measured as the rate of usable samples |
Countries
France
Contacts
CONTACTCindy NEUZILLET, MD, PhD
CONTACTMarie-Emmanuelle Legrier
STUDY_DIRECTORCindy NEUZILLET, MD, PhD
Hôpital PAUL BROUSSE
Outcome results
None listed