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Phase 2 N=69 Treatment

Efficacy and Tolerance Evaluation in FOLFIRINOX Dose Adjusted in Elderly Patients With a Metastatic Pancreatic Cancer

Pancreatic Metastatic Cancer · Toxicity

Enrolled (actual)
69
Serious AEs
69.6%
Results posted
Apr 2026
Primary outcome: Primary: Composite Safety and Early Efficacy Assessment in the First 34 Patients — 65.8 pourcentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Oxaliplatine (Drug); Folinic acid (Drug); Irinotecan (Drug); 5-FU (Drug)
Age
Older Adult · 70+ yrs
Sex
All
Sponsor
Institut Cancerologie de l'Ouest
Primary completion
Nov 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Composite Safety and Early Efficacy Assessment in the First 34 Patients
65.8

Summary

Metastatic pancreatic carcinomas represent the 5th cause of cancer death in France (#8000 per year). The median age at diagnosis is 69 and 74 in male and female respectively. When the 5-Fluorouracile has been used as a single agent with a limited efficacy during more than 20 years, the onset of gemcitabine in 1995 has led to a moderate increase of median survival (from 4.41 to 5.65 months) and overall survival at 1 year (2 versus 18%). Recently, in a phase II followed by a phase-III study, a French collaborative group has demonstrated the benefit of "FOLFIRINOX " regimen versus gemcitabine alone, in terms of median survival (11.1 versus 6.8 months), progression-free survival (6.4 versus 3.3 months) and response rate (31.6 versus 9.4%). Although more hematologic (neutropenia) and GI toxicities were observed, FOLFIRINOX was acceptable as a new standard regimen for the majority of patients under the age of 70 with a good Performans Status. To reduce the toxicity of FOLFIRINOX in elderly patients (> 70 yo), pharmacogenetic monitoring of 5-FU and Irinotecan key metabolism enzymes (DPD and UGTA1) may be easily performed. The methodology of the study is to use the Bryant & Day statistical method, allowing to consider simultaneously as principal objective, the response rate (efficacy) and the tolerance (preservation of autonomy daily living, Katz index): this design is particularly fitting in a study for elderly patients who represent half of the pancreatic carcinoma population.

Eligibility Criteria

Inclusion Criteria

  • Histologically proven ductal pancreatic carcinoma
  • Metastatic disease
  • First-line treatment : No previous chemotherapy in metastatic stage but adjuvant treatment before relapse (secondary metastatic) is permitted, provide it has been administered more than 6 months before)
  • Age of 70 yo or above
  • Normal DPD enzyme level or partial defect (excluding total defect)
  • Adequate bone marrow reserve: as indicated by : neutrophils >1500/mm3, platelets >100,000/ mm3, Hb >10.0g/dL.
  • Adequate Renal function as indicated by: MDRD creatinine clearance > 50ml/min.
  • Adequate hepatic function as indicated by: serum bilirubin 2
  • Inflammatory bowel disease localized on the colon or rectum; bowel obstruction or severe uncontrolled diarrhea
  • Previous or concomitant malignancies other than effectively treated carcinoma in situ of the cervix or non-melanoma skin cancer
  • Hereditary fructose intolerance
  • Persons deprived of liberty or under guardianship
  • Any social, geographical or psychological condition which would compromise the ability to fully comply with the trial procedures and treatments
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02143219). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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