Metformin Combined With Chemotherapy for Pancreatic Cancer (GEM)
A Phase II, Randomized, Placebo Controlled Study to Evaluate the Efficacy of the Combination of Gemcitabine, Erlotinib and Metformin in Patients With Locally Advanced and Metastatic Pancreatic Cancer
調査の概要
詳細な説明
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.
研究の種類
入学 (実際)
段階
- フェーズ2
連絡先と場所
研究場所
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Amsterdam、オランダ、1105AZ
- Academic Medical Center
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:4倍
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的: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.
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Gemcitabine at a dose of 1000 mg/m2 (iv, 30 minutes) will be given weekly, for 3 weeks, followed by one week without gemcitabine
他の名前:
Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food
他の名前:
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.
他の名前:
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プラセボコンパレーター: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.
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Gemcitabine at a dose of 1000 mg/m2 (iv, 30 minutes) will be given weekly, for 3 weeks, followed by one week without gemcitabine
他の名前:
Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food
他の名前:
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.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
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Survival after 6 months
時間枠:6 months after completion of the study
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6 months after completion of the study
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二次結果の測定
結果測定 |
時間枠 |
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Progression free survival
時間枠:6 months after the completion of the study
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6 months after the completion of the study
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Objective response rate
時間枠:expected treatment duration 2- 6 months
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expected treatment duration 2- 6 months
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toxicity profile
時間枠:during study and 4 weeks after stop study medication
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during study and 4 weeks after stop study medication
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協力者と研究者
捜査官
- 主任研究者:Hanneke Wilmink, MD, PhD、Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
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