Metastatic Pancreatic Cancer
Conditions
Keywords
mTOR inhibition, EGFR inhibition, pancreatic cancer, pharmacodynamics
Brief summary
In this study the investigators want to determine the activity and safety of concurrent interruption of the MAPK and PI3K pathways by EGFR and mTOR inhibition in patients with metastatic pancreatic cancer.
Detailed description
This phase I/II non randomized single center study will be performed as a two step design. Part I is dose finding, whereby dose escalations will be performed for everolimus and capecitabine. Part II is the efficacy study. At the MTD doses in part II biomarker studies will be performed in blood and tumor tissue. Study design phase I part: The first week patients will be treated with everolimus alone. Capecitabine will be administered for 14 days in a 3 weekly cycle, starting on day 8. Cetuximab will be administered weekly, starting at day 8. The dose is fixed for cetuximab during study treatment, whereas the doses of everolimus and capecitabine will differ per dose level. First dose level: Everolimus 5 mg daily continuously, Capecitabine 600 mg/m2 bid for 2 weeks every 3 weeks, Cetuximab 400mg/m2 (120 min infusion) first dose, thereafter 250 mg/m2 (60 min infusion) weekly. Second dose level: Everolimus 10 mg daily continuously, Capecitabine 600 mg/m2 bid for 2 weeks every 3 weeks, Cetuximab 400mg/m2 (120 min infusion) first dose, thereafter 250 mg/m2 (60 min infusion) weekly. Third dose level: Everolimus 10 mg daily continuously, Capecitabine 800 mg/m2 bid for 2 weeks every 3 weeks, Cetuximab 400mg/m2 (120 min infusion) first dose, thereafter 250 mg/m2 (60 min infusion) weekly. Study design phase II part At the MTD 14-25 patients with pancreatic cancer will be included. In the phase II part, everolimus will be administered during one week before start of cetuximab. At day 8 the first dose of cetuximab will be administered. Capecitabine will be started one week thereafter. This enables us to perform pharmacodynamic studies to assess biomarker changes during the different phases of treatment. Everolimus will be administered continuously in a dose of 5 or 10 mg orally once daily (dependent on MTD from part 1). Capecitabine will be administered orally in a dose of 400 - 800 mg/m2 twice daily for 14 days followed by one week rest (dependent on MTD from part 1). Patients will receive cetuximab infusions via an infusion pump, with an initial dose of 400 mg/m² (over 120 min) and subsequent weekly infusions of 250 mg/m² (over 60 min), starting day 8.
Interventions
DRUGCapecitabine
Capecitabine will be administered for 14 days in a 3 weekly cycle, starting on day 8.
DRUGCetuximab
Cetuximab will be administered weekly, starting at day 8.
DRUGEverolimus
Everolimus will be administered daily, starting on day 1.
Sponsors
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Signed informed content obtained prior to treatment * Cytological or histological confirmed adenocarcinoma of the pancreas * Metastatic pancreatic cancer * Measurable lesion according to RECIST criteria * ECOG/ WHO performance 0-2 * Age \> 18 years * Life expectancy \> 3 months * Adequate renal function (creatinine \< 150 µmol/L) * Adequate liver function (bilirubin \< 1.5 times upper limit of normal, ALAT or ASAT \< 5.0 times upper limit of normal in case of liver metastases and \< 2.5 the upper limit of normal in absence of liver metastases * Adequate bone marrow function (WBC \> 3.0 x 10 9/L, platelets \> 100 x 10 9/L) * Mentally, physically, and geographically able to undergo treatment and follow up
Exclusion criteria
* Clinical or radiological evidence of CNS metastases * Pregnancy (positive serum pregnancy test) and lactation * Serious concomitant systemic disorder that would compromise the safety of the patient, at the discretion of the investigator * Patients who have any severe and/or uncontrolled medical conditions * Previous treatment with an mTOR inhibitor
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| phase I part: assessment of the dose limiting toxicity | During treatment: assessments on day 1 every cycle (3 weeks). After treatment: every 3 months during the first 2 years, and every 6 months thereafter |
| phase II part: response rate | Assessments after every 3 cycles (9 weeks). |
Secondary
| Measure | Time frame |
|---|---|
| Time to treatment failure | Every 3 months during the first 2 years, and every 6 months thereafter. |
| Overall survival | Every 3 months during the first 2 years, and every 6 months thereafter. |
| Toxicity profile | During treatment: assessments on day 1 every cycle (3 weeks). After treatment: every 3 months during the first 2 years, and every 6 months thereafter. |
| Pharmacodynamics: biomarkers in blood and tumor tissue | Day 1, 8 and 22 during treatment |
Countries
Netherlands
Outcome results
None listed