Esophageal Cancer Clinical Trial
Official title:
A Pilot Study With Cetuximab and Radiation Therapy for Patients With Surgically Resectable Esophageal and GE Junction Carcinomas: Hoosier Oncology Group Study (GI05-92)
The interaction of epidermal growth factor receptor (EGFR) inhibitory agents such as
cetuximab combined with radiation shows promising results. EGFR inhibitory agents also
enhance radiation-induced apoptosis and inhibit radiation induced damage repair. These
interactions may represent the principle effects that contribute to the synergy between EGFR
and radiation.
This trial will investigate the feasibility and activity of this combination in patients
with surgically resectable disease.
OUTLINE: This is a multi-center study.
- Cetuximab 400 mg/m2 IV over 120 minutes Day -14 (Loading Dose)
- Cetuximab 250 mg/m2 IV over 60 minutes, day -7.
- Cetuximab 250 mg/m2 IV over 60 minutes, days 1, 8, 15, 22, 29 and 36.
- External beam radiation therapy, beginning on day 1, 4500 cGy to esophagus with boost
of 540 cGy at 180 cGy per fraction for 6 weeks.
- Surgical resection of primary tumor and adjacent mediastinal and/or celiac lymph nodes
by a transthoracic approach after satisfactory hematologic and functional recovery
within 8 weeks of completion of radiation therapy.
- For patients who give their consent, fresh frozen tissue will be obtained per EUS at
baseline, per EUS 2 weeks after the initiation of cetuximab, and at the time of surgery
for pathology submission.
;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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