This Phase I/II clinical trials aims to determine the response rate of cisplatin and gemcitabine as induction therapy of locally advanced pancreatic cancer; to determine the maximun tolerable dose of gemcitabine-cisplatin chemotherapy combined with radiation therapy in a Phase I study , in order to define an appropriate Phase II dose regimen and to determine the overall response rates of this combined modality regimen following induction chemotherapy; to determine the resectability rate for locally advanced lesions treated with this regimen; and to determine the time to failure for the entire treatment program.

Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
38
Fiscal Year
1999
Total Cost
Indirect Cost
Name
New York University
Department
Type
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10016
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