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

Official title

Pilot Study of Personalized First-line Chemotherapy Choice for Patients With Advanced Pancreatic Adenocarcinoma Using Transcriptomic Signatures (PACsign)

Overview

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

• Other 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.
• Other 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

Primary outcome measures

• Objective Response Rate (ORR) at 4 months based on thorax-abdomen-pelvis (TAP) CT scan every 8 weeks according to RECIST v1.1. [Time frame: 4 months]

Secondary outcome measures (5)

• Progression-Free Survival (PFS) [Time frame: 18 months]
• Overall Survival (OS) [Time frame: 18 months]
• Disease Control Rate (DCR) [Time frame: 18 months]
• Treatment-related severe (grade 3-5) toxicities [Time frame: 18 months]
• Feasibility of study procedure [Time frame: 12 months]

Eligibility criteria

Inclusion criteria

• Written informed consent obtained from the patient prior to performing any protocol-related procedures, including screening evaluations.
• 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.
• Histologically or cytologically proven Pancreatic Ductal Adenocarcinoma (PDAC).
• Metastatic disease.
• Measurable or evaluable lesions according to RECIST v1.1 criteria.
• First-line therapy (previous neoadjuvant/adjuvant chemotherapy not allowed).
• Age ≥ 18 years (no upper limit, patients ≥ 75 years old must have a G8 score ≥ 14).
• 3\. Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0-1.
• Availability of tumor tissue sample from the primary pancreatic tumor or liver metastasis (chemo-naïve) before inclusion in step 1.
• Adequate organ function, as defined by the following (blood test ≤ 7 days prior to inclusion):

• Serum aspartate aminotransferase (AST) and serum alanine aminotransferase (ALT) ≤ 3 x upper limit of normal (ULN) (≤ 5 ULN in case of liver metastases)
• Total serum bilirubin ≤ 1.5 ULN
• Serum albumin ≥ 28 g/L
• Hemoglobin ≥ 9.0 g/dl
• Absolute neutrophil count (ANC) ≥ 1,500/μL
• Platelets ≥ 100,000/μL
• Creatinine clearance ≥ 50 mL/min (MDRD).
• No Dihydropyrimidine dehydrogenase (DPD) deficiency (normal uracil level).
• Life expectancy ≥ 3 months.
• a. Evidence of post-menopausal status b. (or) negative urinary or serum pregnancy test for female pre-menopausal patients.
• Registration in a National Health Care System.

Exclusion criteria

• Concurrent enrolment in another interventional clinical study.
• Previous treatment with chemotherapy for pancreatic cancer.
• Uncontrolled massive pleural effusion or massive ascites.
• Known deficiency in UGT1A1 (homozygous UGT1A1\*28 allele).
• 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).
• 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.
• 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).
• 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.
• Live vaccine administration within 30 days prior to the first dose of study treatment.
• Known or suspected allergy or hypersensitivity to any of the study drugs or any of the study drug excipients.
• 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.
• 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.
• Major surgical procedure (as defined by the Investigator) within 4 weeks prior to the first dose of trial treatment.
• Pregnancy/lactation.
• Person under legal protection or tutelage or guardianship.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Diagnostic

Study locations

France · 7 centers

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

Identifiers

NCT: NCT05475366 · IC 2021-15

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗