Pancreas Neoplasms
Conditions
Keywords
adenocarcinoma of the pancreas, pancreatic cancer, pancreas carcinoma, advanced pancreatic cancer, metastatic pancreatic cancer, second line, palliative, Oxaliplatin, Docetaxel, Taxotere, Eloxatin, Cancer of pancreas, Pancreas cancer
Brief summary
The purpose of this study is to test a combination-therapy of oxaliplatin and docetaxel in patients with metastatic or locally advanced adenocarcinoma of the pancreas after failure of a palliative first line therapy.
Detailed description
For years Fluorouracil was the established treatment for pancreatic cancer with median survival times up to 8 months. Since 1997 Gemcitabine is also a standard therapy with in comparison to Fluorouracil a significant better clinical benefit. But after progression of the disease under a palliative first-line therapy there is no established second line therapy for pancreatic cancer. So the purpose of this study is to test the combination of Oxaliplatin and Docetaxel in patients with metastatic or locally advanced adenocarcinoma of the pancreas after failure of a palliative first line therapy to get a reasonable second line concept.
Interventions
DRUGDocetaxel
75 mg/m2 IV on day 1 of each 22 day cycle
DRUGOxaliplatin
80 mg/m2 IV on day 2 of each 22 day cycle
Sponsors
University of Ulm
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Dated and signed informed concent * Histologically or cytologically proven metastatic or locally advanced adenocarcinoma of the exocrine pancreas (stadium UICC III/IV) * Presence of at least one measurable (according to RECIST criteria) marker lesion (primary tumor or metastasis) outside of an area that was previously subjected to radiation therapy * Failure of a palliative first line therapy of a metastatic or locally advanced adenocarcinoma of the exocrine pancreas due to: Progress within 3 months after a first-line therapy Discontinuation of a first-line therapy due to toxicity * Age \>= 18 years * Karnofsky index \> 60% * Expected live span \> 12 weeks * Sufficient bone marrow reserve: Granulocytes \>= 1.5 x 109/L and Platelets \>= 100 x 109/L and Hemoglobin \>= 9 g/L * Serum Bilirubin \< 2 x upper normal limit or 2.5 x upper normal limit in case of hepatic metastasis (biliary drainage allowed) * AST/ALT \< 2.5 x upper normal limit
Exclusion criteria
* Every other cancer or secondary cancer besides the basal cell carcinoma of the skin or the carcinoma in situ of the cervix uteri. Inclusion of patients with other types of cancer that were successfully treated and that did not relapse within the last 5 years is possible * Pregnancy or lactation * Patients able to reproduce that do not adhere to strict contraception * Presence of brain metastasis * Severe, uncontrolled infection * Preexisting peripheral neuropathy \> grade I * Preexisting severe illnesses such as unstable coronary artery disease or uncontrolled cardiac arrhythmia * Justified disbelief in the compliance of the patient * Parallel participation in another clinical trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| tumor response | 12/2009 and end of the study 12/2010 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| progression free survival | 12/2009 and end of study 12/2010 | — |
| overall survival | 12/2009 and end of study 12/2010 | — |
| Questionnaire for quality of life | every three weeks | — |
| Questionnaire for clinical Benefit | every week | — |
| toxicity / safety | every week | all adverse events will be documented every week with their correlation to Oxaliplatin and Docetaxel |
Countries
Germany
Contacts
Primary ContactThomas Seufferlein, Prof. Dr.
Backup ContactGoetz von Wichert, PD Dr.
Outcome results
None listed