Pancreatic Cancer, Thromboembolism
Conditions
Keywords
thromboembolism, stage III pancreatic cancer, stage IV pancreatic cancer, adenocarcinoma of the pancreas, recurrent pancreatic cancer, stage II pancreatic cancer
Brief summary
RATIONALE: Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Anticoagulants, such as dalteparin, may help prevent blood clots from forming in patients being treated with gemcitabine for pancreatic cancer. PURPOSE: This randomized phase II trial is studying how well gemcitabine works with or without dalteparin in treating patients with locally advanced or metastatic pancreatic cancer.
Detailed description
OBJECTIVES: Primary * Compare the incidence of venous thromboembolism in patients with locally advanced or metastatic pancreatic cancer treated with gemcitabine hydrochloride and dalteparin versus gemcitabine hydrochloride alone. Secondary * Compare the survival benefit, in terms of increased (from 70% to 85%) survival at 12 weeks, of patients treated with these regimens. * Compare the toxicity of these regimens. * Compare the overall survival of patients treated with these regimens. * Compare the time to disease progression in patients treated with these regimens. * Determine the effect of gemcitabine hydrochloride and dalteparin on serological markers of thromboangiogenesis. OUTLINE: This is a multicenter, randomized study. Patients are stratified according to disease progression (locally advanced vs metastatic) and Karnofsky performance status (≥ 80% vs \< 80%). Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive gemcitabine hydrochloride IV over 30 minutes once weekly in weeks 1-7 and 9-11. * Arm II: Patients receive low molecular weight dalteparin subcutaneously once daily in weeks 1-12. Patients also receive gemcitabine hydrochloride as in arm I. Blood samples are acquired at baseline for analysis of circulating tissue factor and vascular endothelial growth factor. After completion of study treatment, patients are followed periodically. PROJECTED ACCRUAL: A total of 120 patients will be accrued for this study.
Interventions
DRUGdalteparin
DRUGgemcitabine hydrochloride
OTHERdiagnostic laboratory biomarker analysis
Sponsors
Hull University Teaching Hospitals NHS Trust
Study design
Allocation
RANDOMIZED
Primary purpose
TREATMENT
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Histologically or cytologically confirmed metastatic or locally advanced adenocarcinoma of the pancreas * Patients with clinical 'high probability' of pancreatic cancer and biopsy suggestive but not diagnostic of pancreatic cancer may be eligible based on review by the principal investigator * Measurable or evaluable disease * No clinical evidence of active venous thromboembolism PATIENT CHARACTERISTICS: * Karnofsky performance status (PS) 60-100% OR WHO PS 0-2 * Life expectancy \> 12 weeks * Absolute neutrophil count \> 2,000/mm³ * WBC \> 3,000/mm³ * Platelet count \> 100,000/mm³ * Creatinine clearance \> 50 mL/min * INR ≤ 1.5 times upper limit of normal (ULN) * Bilirubin \< 1.5 times ULN (stent allowed) * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception * No cerebrovascular accident within the past 6 months * No obvious contraindication to anticoagulation, including the following: * Bleeding diathesis * Active peptic ulcer * Ulcerating cancer into duodenum * No history of other advanced malignancy * No gross hematuria * No melaena or gross evidence of gastrointestinal bleeding (other than piles) * No requirement for a central line * No other significant medial or psychiatric illness that, in the opinion of the investigator, would preclude study participation PRIOR CONCURRENT THERAPY: * No prior gemcitabine hydrochloride-containing treatment * No other concurrent cytotoxic chemotherapy, immunotherapy, hormonal therapy (excluding contraceptives and replacement steroids), or experimental medications * No other concurrent specific anticancer therapy as a result of disease progression * No concurrent caval filter device * No other concurrent anticoagulants for venous thromboembolism or other reasons (e.g., atrial fibrillation) * No concurrent acetylsalicylic acid (\> 75 mg) as an antiplatelet drug for a preexisting cardiovascular condition * No concurrent clopidogrel bisulfate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of venous thromboembolism reduction | — |
Secondary
| Measure | Time frame |
|---|---|
| Overall survival | — |
| Time to disease progression | — |
| Effect of drug combination on serological markers of thromboangiogenesis | — |
| Early survival benefit | — |
| Toxicity | — |
Countries
United Kingdom
Outcome results
None listed