S0205 Gemcitabine w/ or w/o Cetuximab as First-Line Therapy in Locally Advanced Pancreas Cancer
Basic Trial Information
|Phase III||Treatment||Completed||Not specified||NCI, Other||CDR0000347414|
S0205, CALGB-S0205, CAN-NCIC-PAC1, U10CA032102, SWOG-S0205, PAC1, NCT00075686
RATIONALE: Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop tumor cells from dividing so they stop growing or die. Monoclonal antibodies, such as cetuximab, can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. It is not yet known whether gemcitabine is more effective with or without cetuximab in treating pancreatic cancer.
PURPOSE: This randomized phase III trial is studying giving gemcitabine together with cetuximab to see how well it works compared to giving gemcitabine alone as first-line therapy in treating patients with locally advanced unresectable or metastatic adenocarcinoma of the pancreas.
Further Study Information
- Compare the overall survival of patients with locally advanced unresectable or metastatic adenocarcinoma of the pancreas treated with gemcitabine and cetuximab vs gemcitabine alone.
- Compare the time to treatment failure in patients treated with these regimens.
- Estimate the percentage of patients with epidermal growth factor receptor (EGFR) tumor expression in patients treated with these regimens.
- Compare the overall survival of patients in the EGFR-positive subset treated with these regimens.
- Compare the toxicity of these regimens in these patients.
- Compare the total response rate (confirmed and unconfirmed complete and partial response) in patients with measurable disease treated with these regimens.
- Compare the patient report of pain and quality of life of patients treated with these regimens.
OUTLINE: This is an open-label, randomized, multicenter study. Patients are stratified according to disease status (locally advanced unresectable vs metastatic), Zubrod performance status (0 or 1 vs 2), and prior pancreatectomy (yes vs no). Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive cetuximab IV over 1-2 hours on days 1, 8, 15, and 22 and gemcitabine IV over 30 minutes on days 1, 8, 15, and 22 for course 1 and days 1, 8, and 15 for all subsequent courses.
- Arm II: Patients receive gemcitabine as in arm I. In both arms, courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.
Quality of life is assessed at baseline, before each course, and at the end of study therapy.
Patients are followed every 6 months for 2 years and then annually for 1 year.
PROJECTED ACCRUAL: A total of 704 patients (352 per treatment arm) will be accrued for this study within 5 years.
- Histologically* or cytologically confirmed pancreatic adenocarcinoma meeting 1 of the following criteria:
- Locally advanced unresectable disease
- Distant metastatic disease NOTE: If diagnosis is based on a metastatic site the histology must be compatible with pancreatic cancer
- Measurable or nonmeasurable disease by x-ray, scan, or physical examination
- Tumor tissue must be submitted for evaluation of epidermal growth factor receptor expression before study entry
- None of the following tumor types are allowed:
- Endocrine tumors
- Lymphoma of the pancreas
- Ampullary cancer
- No known brain metastases
- Not specified
- Zubrod 0-2
- At least 3 months
- Absolute granulocyte count at least 1,500/mm^3
- Platelet count at least 100,000/mm^3
- Bilirubin no greater than 2.0 times upper limit of normal (ULN)
- SGOT or SGPT no greater than 2.5 times ULN
- Creatinine no greater than 2.0 mg/dL
- No significant history of cardiac disease
- No uncontrolled hypertension
- No unstable angina
- No uncontrolled arrhythmia
- No congestive heart failure
- Not pregnant or nursing
- Fertile patients must use effective contraception
- HIV negative
- No other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, or adequately treated stage I or II cancer that is currently in remission
PRIOR CONCURRENT THERAPY:
- No prior immunotherapy for advanced pancreatic cancer
- No prior cetuximab or other therapy that targets the epidermal growth factor pathway
- No prior chimerized or murine monoclonal antibody therapy
- No other concurrent anticancer immunotherapy
- At least 6 months since prior adjuvant chemotherapy
- No prior chemotherapy or chemoradiotherapy for advanced pancreatic cancer
- No prior gemcitabine
- No other concurrent anticancer chemotherapy
- No prior hormonal therapy for advanced pancreatic cancer
- No concurrent anticancer hormonal therapy
- See Chemotherapy
- At least 28 days since prior radiotherapy and recovered
- Prior palliative radiotherapy to metastatic sites allowed
- No concurrent anticancer radiotherapy, including whole brain radiotherapy for progressive disease (i.e., CNS metastasis)
- At least 14 days since prior pancreatic cancer surgery and recovered
- No other concurrent anticancer therapy
Trial Contact Information
Trial Lead Organizations/Sponsors
Southwest Oncology Group
- National Cancer Institute
- Cancer and Leukemia Group B
- NCIC-Clinical Trials Group
Link to the current ClinicalTrials.gov record.
NLM Identifier NCT00075686
ClinicalTrials.gov processed this data on April 07, 2015
Note: Information about this trial is from the ClinicalTrials.gov database. The versions designated for health professionals and patients contain the same text. Minor changes may be made to the ClinicalTrials.gov record to standardize the names of study sponsors, sites, and contacts. Cancer.gov only lists sites that are recruiting patients for active trials, whereas ClinicalTrials.gov lists all sites for all trials. Questions and comments regarding the presented information should be directed to ClinicalTrials.gov.