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A Phase III Trial Evaluating the Addition of Cetuximab to Paclitaxel, Cisplatin, and Radiation for Patients With Esophageal Cancer Who Are Treated Without Surgery
Primary
To evaluate if the addition of cetuximab to paclitaxel, cisplatin, and radiation improves overall
survival compared to paclitaxel, cisplatin, and radiation alone in patients with esophageal
cancer who are treated without surgery.
Secondary
To evaluate if the addition of cetuximab to paclitaxel, cisplatin, and radiation improves local
control by increasing the clinical complete response and decreasing local recurrence for
patients with esophageal cancer who are treated without surgery.
To evaluate adverse events.
To evaluate endoscopic complete response rates.
To evaluate if the addition of cetuximab to paclitaxel, cisplatin, and radiation improves the
Esophageal Cancer Subscale score of the FACT-E quality of life tool.
To evaluate the quality-adjusted survival of each treatment arm using EQ-5D if the primary
endpoint supports the primary hypothesis.
To implement a well-controlled tissue handling/storage protocol to facilitate future laboratory
correlative studies.
Primary
To evaluate if the addition of cetuximab to paclitaxel, cisplatin, and radiation improves overall
survival compared to paclitaxel, cisplatin, and radiation alone in patients with esophageal
cancer who are treated without surgery.
Secondary
To evaluate if the addition of cetuximab to paclitaxel, cisplatin, and radiation improves local
control by increasing the clinical complete response and decreasing local recurrence for
patients with esophageal cancer who are treated without surgery.
To evaluate adverse events.
To evaluate endoscopic complete response rates.
To evaluate if the addition of cetuximab to paclitaxel, cisplatin, and radiation improves the
Esophageal Cancer Subscale score of the FACT-E quality of life tool.
To evaluate the quality-adjusted survival of each treatment arm using EQ-5D if the primary
endpoint supports the primary hypothesis.
To implement a well-controlled tissue handling/storage protocol to facilitate future laboratory
correlative studies.
Recruitment Status
Past Studies