Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Michigan Rogel Cancer Center
With
Sanofi-Synthelabo
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patients must have cytologic or histologic confirmation of carcinoma arising in the pancreas.
Patients may have any stage of pancreatic cancer but if metastatic, systemic disease burden should be asymptomatic and small in volume.
Determination of resectability must be made prior to registration.
Patients must have an estimated life expectancy of at least 12 weeks and a Zubrod performance status of \< = 2.
Patients must have adequate organ function defined as follows: absolute neutrophil count of \> = 1500/mm3, platelets \> = 100,000/mm3, serum Cr \< = 1.5 mg/dl, bilirubin \< 3.0 mg/dl, with relief of biliary obstruction if present (PTC tube or endobiliary stent).
Patients must be free of other active systemic malignancy, ongoing infection, including HIV infection, or any other serious uncontrolled, concomitant systemic disorders or psychiatric condition that would interfere with the safe delivery of protocol therapy.
Patients of reproductive potential must have agreed to use an effective contraceptive method during participation in this trial and for 6 months after trial.
Patient must be aware of the investigational nature of the therapy and provide written informed consent.
You may not be if
Patients with neuroendocrine tumors are excluded.
Patients must have no history of previous chemotherapy for pancreatic cancer or any abdominal radiation therapy.
Patient must not have used any investigational agent in the month before enrollment into the study.
Clareo Health | Gemcitabine, Oxaliplatin and Radiation Therapy in Pancreatic Cancer
