Metformin Combined With Chemotherapy for Pancreatic Cancer
Lykilorð
Útdráttur
Lýsing
In this phase II randomized, placebo controlled study, patients with locally advanced or metastatic pancreatic cancer will be randomized to treatment with gemcitabine, erlotinib and metformin, or gemcitabine, erlotinib and placebo.
Gemcitabine at a dose of 1000 mg/m2 (iv, 30 minutes) will be given weekly, for 3 weeks, followed by one week without treatment. Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food. Metformin/ placebo will be administered at a dose of 500 mg twice daily. If well tolerated the dose will be increased to 1000 mg twice daily in the second week.
Dagsetningar
Síðast staðfest: | 08/31/2010 |
Fyrst lagt fram: | 09/27/2010 |
Áætluð skráning lögð fram: | 09/27/2010 |
Fyrst sent: | 09/28/2010 |
Síðasta uppfærsla lögð fram: | 05/18/2014 |
Síðasta uppfærsla sett upp: | 05/19/2014 |
Raunverulegur upphafsdagur náms: | 07/31/2010 |
Áætlaður aðallokunardagur: | 01/31/2014 |
Áætlaður dagsetningu rannsóknar: | 03/31/2014 |
Ástand eða sjúkdómur
Íhlutun / meðferð
Drug: gemcitabine
Drug: erlotinib
Drug: Gemcitabine, erlotinib and metformin
Drug: Gemcitabine, erlotinib and placebo
Stig
Armhópar
Armur | Íhlutun / meðferð |
---|---|
Experimental: Gemcitabine, erlotinib and metformin Gemcitabine at a dose of 1000 mg/m2 (iv, 30 minutes) will be given weekly, for 3 weeks, followed by one week without gemcitabine. Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food. Metformin will be administered at a dose of 500 mg twice daily. If well tolerated the dose will be increased to 1000 mg twice daily in the second week. | Drug: Gemcitabine, erlotinib and metformin Metformin will be administered at a dose of 500 mg twice daily for the first week. If tolerated well, the dose will be increased up to 1000 mg twice daily in the second week. |
Placebo Comparator: Gemcitabine, erlotinib and placebo Gemcitabine at a dose of 1000 mg/m2 (iv, 30 minutes) will be given weekly, for 3 weeks, followed by one week without gemcitabine. Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food. PLacebo will be administered at a dose of 500 mg twice daily. If well tolerated the dose will be increased to 1000 mg twice daily in the second week. | Drug: Gemcitabine, erlotinib and placebo Placebo will be administered at a dose of 500 mg twice daily for the first week. If tolerated well, the dose will be increased up to 1000 mg twice daily in the second week. |
Hæfniskröfur
Aldur hæfur til náms | 18 Years Til 18 Years |
Kyn sem eru hæf til náms | All |
Tekur við heilbrigðum sjálfboðaliðum | Já |
Viðmið | Inclusion Criteria: - Signed informed content obtained prior to treatment - Cytological or histological confirmed carcinoma of the pancreas - Metastatic cancer - Measurable lesion according to RECIST criteria - ECOG/ WHO performance 0-2 - Age > 18 years - Adequate renal function (creatinine < 150 µmol/L and/ or a creatinine clearance > 60 ml/ 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: - unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction ≤ 6 months prior to randomization, serious uncontrolled cardiac arrhythmia - uncontrolled diabetes as defined by fasting serum glucose >2X ULN. - active or uncontrolled severe infection. - cirrhosis, chronic active hepatitis or chronic persistent hepatitis - severely impaired lung function - Previous treatment with erlotinib - Previous treatment with gemcitabine for metastatic disease - Previous treatment with gemcitabine combined with radiotherapy for locally advanced pancreatic cancer within 6 months prior to study entry - Patients with a known hypersensitivity to metformin - Use of metformin in the previous 6 months |
Útkoma
Aðal niðurstöður ráðstafanir
1. Survival after 6 months [6 months after completion of the study]
Aðgerðir vegna aukaatriða
1. Progression free survival [6 months after the completion of the study]
2. Objective response rate [expected treatment duration 2- 6 months]
3. toxicity profile [during study and 4 weeks after stop study medication]