DHA-Paclitaxel in Treating Patients With Metastatic Pancreatic Cancer
Pancreatic Cancer
About this trial
This is an interventional treatment trial for Pancreatic Cancer focused on measuring recurrent pancreatic cancer, stage IV pancreatic cancer
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically or cytologically confirmed carcinoma of the pancreas Metastatic disease Measurable disease Lesions within a previously irradiated field are not considered measurable No islet cell tumors, lymphoma, or sarcoma of the pancreas No known or clinical evidence of CNS metastasis PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-1 Life expectancy: Not specified Hematopoietic: Absolute neutrophil count at least 1,500/mm^3 Platelet count at least 100,000/mm^3 Hepatic: Bilirubin no greater than 1.5 times upper limit of normal (ULN) SGOT or SGPT no greater than 2.5 times ULN Renal: Creatinine no greater than 1.5 times ULN Cardiovascular: No uncontrolled ventricular arrhythmia No myocardial infarction within the past 3 months No superior vena cava syndrome Neurologic: No peripheral neuropathy greater than grade 1 No uncontrolled major seizure disorder No spinal cord compression Other: No concurrent serious infection requiring parenteral therapy No unstable or serious concurrent medical condition No other prior malignancy except: Curatively treated nonmelanoma skin cancer or carcinoma in situ of the cervix OR Other cancer curatively treated with surgery alone that has not recurred for more than 5 years No psychiatric disorder that would preclude study compliance Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception during and for 6 months after study therapy PRIOR CONCURRENT THERAPY: Biologic therapy: No concurrent immunotherapy Chemotherapy: No prior chemotherapy for metastatic disease Prior adjuvant chemoradiotherapy allowed At least 28 days since prior chemotherapy and recovered No other concurrent chemotherapy Endocrine therapy: No concurrent hormonal therapy except megestrol Radiotherapy: See Disease Characteristics Prior adjuvant chemoradiotherapy allowed At least 28 days since prior large-field radiotherapy and recovered No concurrent radiotherapy Surgery: At least 14 days since prior major surgery and recovered Other: No other concurrent anticancer therapy
Sites / Locations
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
- NYU School of Medicine's Kaplan Comprehensive Cancer Center
- Kimmel Cancer Center of Thomas Jefferson University - Philadelphia
- Virginia Mason Medical Center
- Kliniken Essen - Mitte
- Krankenhaus Nordwest
- Erasmus Medical Center
- New Cross Hospital
- Beatson Oncology Centre