Vitamin C to Quality of Life in Patients With Terminal Stage Pancreatic Cancer (PTCA199-4)
Metastatic Pancreatic Cancer, Terminal Cancer
About this trial
This is an interventional treatment trial for Metastatic Pancreatic Cancer focused on measuring ascorbate, anemia, quality of life, chemotherapy
Eligibility Criteria
Inclusion Criteria: Ability to understand and the willingness to sign a written informed consent document. Age ≥ 18 years and ≤ 80 years. Eastern Cooperative Oncology Group (ECOG) performance status 0-2. Histologically or cytologically confirmed metastatic pancreas adenocarcinoma. Tumor progression after two lines of chemotherapy. Adequate organ performance based on laboratory blood tests. Presence of at least of one measurable lesion in agreement to Response Evaluation Criteria in Solid Tumours (RECIST) criteria. The expected survival ≥ 1 months. Women of childbearing potential and men must agree to use adequate contraception prior to study entry and for the duration of study participation. Exclusion Criteria: Active second primary malignancy or history of second primary malignancy. The diagnosis was confirmed by pathology as non-adenocarcinoma of pancreas. Inflammation of the digestive tract, including pancreatitis, cholecystitis, cholangitis, etc. Pregnant or nursing women. Glucose-6-phosphate dehydrogenase (G6PD) deficiency. Severe and uncontrollable accompanying diseases that may affect protocol compliance or interfere with the interpretation of results. Renal insufficiency or dialysis Other serious accompanying illnesses, which, in the researcher's opinion, could seriously adversely affect the safety of the treatment. Patients who are unwilling or unable to comply with study procedures.
Sites / Locations
- Shanghai Cancer CenterRecruiting
Arms of the Study
Arm 1
Experimental
Ascorbate
For patients with baseline serum Vitamin C concentration < 65 μmol/L, intravenous Vitamin C 10 g × 7 days, intravenous Vitamin C 4 g × 7 days, intravenous Vitamin C 2 g × 7 days, followed by continuously 900 mg/day, three times a day, orally. For patients with baseline serum Vitamin C concentration ≥ 65 μmol/L, continuously 900 mg/day, three times a day, orally.