Combining Erlotinib Plus Bevacizumab and Gemcitabine Plus Capecitabine to Treat Advanced Pancreatic Cancer

To establish the safety and efficacy of a combination of four drugs (capecitabine, gemcitabine, erlotinib and bevacizumab) in the treatment of patients with locally advanced or metastatic pancreatic cancer. The study will be divided into two parts:

Part A (Phase I ): Is to establish the optimal dose of capecitabine for combination with gemcitabine, bevacizumab and erlotinib. This part of the study is necessary in order to characterise any increased side effects that may occur as a result of this combination of drugs. The dose of capecitabine will be increased in cohorts containing 3 to 6 patients(according to standard dose escalation study design) whilst side effects are closely monitored. The doses of the other three drugs will remain fixed during this period:

• Gemcitabine: 1000 mg/m2 Days 1, 8, 15
• Bevacizumab: 5 mg/kg every two weeks iv
• Erlotinib: 100 mg/day orally

Maximum tolerated dose is the dose at which 2 out of a cohort of three to six patients experience dose-limiting toxicity within the first cycle (28 days) of treatment. The recommended dose for further evaluation will be one dose level below this.

Part B (Phase II): Once a recommended dose of capecitabine has been chosen, this will be used for the remainder of the trial to further characterise the efficacy and safety of the drug combination in this group of patients.

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed adenocarcinoma of the pancreas
• Locally advanced or metastatic disease
• Not amenable to curative resection
• No invasion of adjacent organs (e.g., duodenum or stomach) by CT scan
• Unidimensionally measurable disease as assessed by CT in accordance with the Response Evaluation Criteria in Solid Tumors (RECIST) guidelines.
• No evidence of brain metastasis

PATIENT CHARACTERISTICS:

Age:

• 18 and over

Performance status:

• Eastern Cooperative Oncology Group (ECOG) 0-2

Life expectancy:

• Greater than 3 months

Hematopoietic:

• Granulocyte count ≥ 1,500/mm^3
• Platelet count ≥ 100,000/mm^3

Hepatic:

• Bilirubin ≤ upper limit of normal
• Serum albumin > 26 g/litre

Renal:

• Creatinine ≤ 180 micromoles/litre OR
• Creatinine clearance ≥ 50 mL/min

Cardiovascular:

• No clinically significant cardiovascular disease
• No uncontrolled hypertension (i.e., blood pressure > 150/90 mm Hg on medication)
• No arterial thromboembolic event within the past 6 months, including any of the following:

• Myocardial infarction
• Unstable angina pectoris
• Cerebrovascular accident
• Transient ischemic attack
• No New York Heart Association grade II-IV congestive heart failure
• No serious cardiac arrhythmia requiring medication

OTHER:

• Not pregnant or breast feeding
• Fertile patients must use effective contraception during study participation
• No serious or non-healing wound, ulcer, or bone fracture
• No infection requiring parenteral antibiotics
• No major bleeding diathesis or coagulopathy
• No significant traumatic injury within the past 28 days
• No surgery within the last 28 days or anticipation for the need for major surgery during the course of study treatment
• No other active malignancy except non-melanoma skin cancer and cervical cancer in-situ
• No history of known dihydropyrimidine dehydrogenase (DPD) deficiency
• No lack of physical integrity of the upper gastro-intestinal tract, malabsorption syndrome, or inability to take oral medication

PRIOR CONCURRENT THERAPY:

• No previous chemotherapy, radiotherapy or other investigational drug treatment for metastatic disease (including VEGF or EGFR antagonists)
• No previous preoperative or adjuvant chemotherapy, radiotherapy or other investigational drug treatment.
• No full dose anti-coagulation (i.e. warfarin or full dose low molecular weight heparin) prior to starting study treatment.
• No ongoing treatment with aspirin (>325 mg/day) or other medications known to predispose to gastrointestinal ulceration