Colorectal Cancer Clinical Trial
Official title:
Phase 3 Study of Enteral Nutrition Rich in Eicosapentaenoic Acid in Patients Receiving Chemotherapy for Gastric Cancer or Colorectal Cancer
Malnutrition is frequently seen in patients on chemotherapy suffering from gastric/colorectal cancer and may worsen the outcome. EPA, a sort of ω-3 PUFA, can modulate immune system. EPA also antagonizes metabolic and inflammatory changes induced by the tumor. This study is to test whether EPA, in combination with enteral nutrition, can improve nutritional/immunologic status, quality of life, and reduce chemotherapy related side effects of these patients.
Chemotherapy is indispensible for patients suffering from advanced gastric or colorectal
cancer, and also the main therapy for those with end-stage tumor. However, incidence of
malnutrition during chemotherapy was reported as high as 60%. The mechanisms include anatomy
modification of digestive tract, side effects of chemotherapy such as anorexia, nausea,
vomiting, and inflammatory factors generated or induced by the tumor. Malnutrition may lead
to discontinuation of the therapy, compromise of the anti-cancer effect, increase of
toxicity and mortality. 20%-40% of patients with end-stage tumor ultimately died from
malnutrition.
EPA (Eicosapentaenoic acid, molecular formula C20H30O2) belongs to ω-3 polyunsaturated fatty
acid (ω-3 PUFA). EPA is one of the main constituent of fish oil. EPA decreases
LPS-stimulated macrophage production of TNF-α, IL-1β, IL-6, and human B lymphocytes
production of IL-10, TNF-α, IFN-γ. EPA can suppress cancer induced lipolysis, and enhanced
the inhibitory effect of 5-Fu over cancer cell proliferation. However, cancer patients are
always lack of EPA.
Nutriall is a sort of non-elemental diet. The kind of powder is produced by Guangdong
Academy of Agriculture Science. Every 50 grams of nutriall contains 9.3mg of VitC and 0.8mg
of VitE. For this enteral nutrition preparation, there have been evidences of protective
effects on nutritional status during chemotherapy on lung cancer. However, this kind of
preparation does not contain EPA.
Up to date, there has been no RCT which testified whether therapeutic dosage of EPA plus
enteral nutrition has combined effects on patients receiving chemotherapy. The investigators
choose nutriall as basic nutritional support agent during chemotherapy, and give patients
different dosage of EPA. Nutritional and immunologic status, quality of life and side
effects of chemotherapy are recorded to evaluate whether EPA can improve outcome of these
patients. Through this study the investigators may also optimize the dose of EPA for
patients receiving chemotherapy on gastric/colorectal cancer.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment
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