Gemcitabine, Oxaliplatin and Radiation Therapy in Pancreatic Cancer

University of Michigan Rogel Cancer Center

Status and phase

Completed

Phase 2

Phase 1

Conditions

Pancreatic Neoplasms

Treatments

Drug: gemcitabine

Drug: oxaliplatin

Procedure: radiation therapy

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00242190

UMCC 2003-082

Details and patient eligibility

About

This study will examine a proposed research treatment which evaluates the addition of oxaliplatin, a chemotherapy agent, to gemcitabine, another chemotherapy agent, and radiation therapy for the treatment of patients with pancreatic cancer. The researchers have already done studies using gemcitabine and radiation therapy together. They want to build on the information they have from this previous research. The researchers believe that the combination chemotherapy with radiation is worth investigating to treat pancreatic cancer. They will use this study to determine what type of side effects occur with this treatment and to assess how effective the treatment is at controlling the cancer.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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.

Exclusion criteria

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.