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NCT02980510CompletedPhase 2

Comparison FOLFIRINOX Panitumumab vs mFOLFOX6 Panitumumab in RAS/B-RAF Wild-type Metastatic Colorectal Cancer Patients

Phase II Randomized Study Comparing FOLFIRINOX + Panitumumab Versus mFOLFOX6 + Panitumumab in Metastatic Colorectal Cancer Patients Selected by RAS and B-RAF Status From Circulating DNA Analysis

Source: ClinicalTrials.gov · Last updated 29 Sept 2026

Brief summary (registry, in English)

National trial, multicenter, randomized, phase II assessing FOLFIRINOX + Panitumumab versus mFOLFOX6 + Panitumumab in metastatic colorectal cancer patients selected by RAS and B-RAF status from circulating DNA analysis. Evaluation of complete response rate on treatment combining FOLFIRINOX and panitumumab.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
219 (actual)
First submitted
30 Nov 2016
Start date
Dec 2016
Primary completion date
Dec 2025
Lead sponsor
UNICANCER
NCT number
NCT02980510
EU CT number
2024-510645-34-00
EudraCT number
2016-001490-33

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 219
  • From Dec 2016 to the primary completion date, Dec 2025
  • 23 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Adjuvant treatment with oxaliplatin
  • Previous treatment for metastatic disease
  • Patients who received any chemo- and/or radiotherapy within 15 days from the date of blood sampling for the RAS and BRAF test
  • Previous organ transplantation, HIV or other immunodeficiency syndromes
  • Concomitant medications/comorbidities that may prevent the patient from receiving study treatment as uncontrolled intercurrent illness (for instance: active infection, active inflammatory disorders, inflammatory bowel disease, intestinal obstruction, symptomatic congestive heart failure, uncontrolled hypertension…)
  • Patient with contraindication for trial drugs (investigators have to refer to SmPC drugs, see Appendix 7)
  • Concomitant intake of St. John's wort
  • Other concomitant cancer

Other illness

  • History of other malignancy within the previous 5 years (except for appropriately treated in-situ cervix carcinoma and non-melanoma skin carcinoma)
  • Patients with a history of severe or life-threatening hypersensitivity to the active substances or to any of the excipients delivered in this study
  • Patient with history of pulmonary fibrosis or interstitial pneumonitis
  • Ionic disorders as:
    • Kalemia ≤1 x LLN
    • Magnesemia \<0.5mmol/L
    • Calcemia \<2mmol/L
  • Patients with psychological, familial, sociological or geographical condition hampering compliance with the study protocol and follow-up schedule

Lab values

  • QT/QTc\>450msec for men and \>470msec for women

Other

  • Brain metastases
  • Persistent peripheral neuropathy \>grade1 (NCI CT v4.03)
  • Patient with known dihydropyrimidine dehydrogenase deficiency
  • Participation in another therapeutic trial
  • Pregnant woman or lactating woman
  • Legal incapacity or limited legal capacity

Who the study is looking for

  • Age between 18 and 75 years
  • ECOG PS between 0 and 1
  • Histologically confirmed adenocarcinoma of the colon or rectum
  • Untreated synchronous or metachronous metastatic disease deemed unresectable with curative intent
  • K-Ras (codons 12, 13, 59, 61, 117, 146), N-Ras (codons 12, 13, 59, 61) and B-Raf (codon 600) wild-type tumor status according to plasma analysis of circulating cell free DNA by Intplex technology
  • Measurable disease according to RECIST version 1.1
  • Adequate hematologic, hepatic and renal functions:
    • Absolute neutrophil count (ANC) ≥2 x 109/L
    • Haemoglobin ≥9 g/dL
    • Platelets (PTL) ≥100 x 109/L
    • AST/ALT ≤5 x ULN
    • Alkaline phosphatase ≤2.5 x ULN
    • Bilirubin ≤1.5 x ULN
    • Creatinine clearance ≥50 mL/min (Cockcroft and Gault formula)
  • Life expectancy of at least 3 months
  • Adequate contraception if applicable
  • Patient affiliated to a social security regimen
  • Patient information and signed written consent form
  • Uracilemia \< 16 ng/ml

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (23)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Institut de Cancerologie de L'Ouest
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AngersFranceActive, not recruiting
Institut Bergonie
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BordeauxFranceActive, not recruiting
Centre Francois Baclesse
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Caen Cedex 5FranceActive, not recruiting
Centr Georges Francois Leclerc
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DijonFranceActive, not recruiting
Groupement Des Hopitaux De L'Institut Catholique De Lille
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Lille CedexFranceActive, not recruiting
Hôpital Privé Jean Mermoz
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LyonFranceActive, not recruiting
Centre Leon Berard
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LyonFranceActive, not recruiting
Hopital Europeen Marseille
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MarseilleFranceActive, not recruiting
Centre De Cancerologue Du Grand Montpellier
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MontpellierFranceActive, not recruiting
Centre Hospitalier Universitaire De Montpellier
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Montpellier Cedex 5FranceActive, not recruiting
Institut Regional Du Cancer De Montpellier
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Montpellier Cedex 5FranceActive, not recruiting
L'Hopital Prive Du Confluent
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Nantes Cedex 2FranceActive, not recruiting
Centre Antoine Lacassagne
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Nice Cedex 2FranceActive, not recruiting
Assistance Publique Hopitaux de Paris
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ParisFranceActive, not recruiting
Centre Catalan d'Oncologie
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PerpignanFranceActive, not recruiting
Centre Hospitalier De Perpignan
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Perpignan CedexFranceActive, not recruiting
Centre Hospitalier Universitaire de Bordeaux
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PessacFranceActive, not recruiting
Hôpital Privé des Côtes d'Armor
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PlérinFranceActive, not recruiting
Institut Godinot
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ReimsFranceActive, not recruiting
Centre Hospitalier Universitaire Reims
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Reims CedexFranceActive, not recruiting
CHU De Rouen
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Rouen CedexFranceActive, not recruiting
Institut De Cancerologie De L Ouest
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St HerblainFranceActive, not recruiting
Institut de cancérologie de Lorraine
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Vandoeuvre Les Nancy_ CedexFranceActive, not recruiting

This page is information, not medical advice. Discuss any trial with your doctor.