Pancreatic Cancer Clinical Trial
Official title:
Phase II Study of Erlotinib (TarcevaTM) Combined With Chemoradiation and Adjuvant Chemotherapy in Patients With Resectable Pancreatic Cancer
To seek preliminary evidence of antitumor activity (progression free survival) of Erlotinib in combination with standard adjuvant chemoradiation and chemotherapy in patients with resected adenocarcinoma of the pancreas.
This study is a phase II trial of erlotinib in combination with chemoradiation in patients
with stage I/II adenocarcinoma of the pancreas who are candidates for adjuvant
chemoradiation.
This study is a phase II trial of erlotinib in combination with chemoradiation in patients
with resected stage I/II adenocarcinoma of the pancreas who are candidates for adjuvant
chemoradiation. Eligible patients will receive adjuvant treatment with erlotinib 100 mg plus
Capecitabine 800 mg/m2 PO BID (5 days on/ 2 days off regimen) and External Beam Radiation
Therapy (EBRT) at doses of 50.4 Gy in 28 fractions after pancreatectomy (Dosing for
capecitabine and erlotinib was amended after considering the toxicity profile of the first 6
patients). Approximately 4-8 weeks after the conclusion of chemoradiation, it is recommended
patients will continue treatment with 4 cycles of gemcitabine 1000 mg/m2 days 1, 8, and 15
every 28 days plus daily erlotinib 100 mg.
Eligible patients will receive adjuvant treatment with erlotinib 100 mg plus Capecitabine 800
mg/m2 PO BID (5 days on/ 2 days off) and External Beam Radiation Therapy (EBRT) to the tumor
bed plus adjacent lymph nodes at doses of 50.4 Gy in 28 fractions after surgery. For patients
with close or positive margins after resection, they will be able to receive 54.0 Gy over 30
fractions. Approximately 4-8 weeks after the conclusion of chemoradiation, it is recommended
patients will continue treatment with 4 cycles of gemcitabine 1000 mg/m2 days 1, 8, and 15
every 28 days plus erlotinib 100 mg/daily.
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