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Effect of Enteral Nutrition Rich in Eicosapentaenoic Acid (EPA) on Patients Receiving Chemotherapy for GI Tumor

Primary Purpose

Gastric Cancer, Colorectal Cancer, Chemotherapy

Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Nutriall
LDEPA
Placebo
HDEPA
Chemotherapy
Sponsored by
Sun Yat-sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastric Cancer focused on measuring gastric cancer, colorectal cancer, chemotherapy, eicosapentaenoic acid, enteral nutrition

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • The cases have undergone radical excision on gastric cancer or colorectal cancer.
  • Without contraindication for chemotherapy.
  • Eligible for postoperative adjuvant XELOX chemotherapy.
  • Capable of taking in food or drug orally.
  • Without severe absorption dysfunction
  • Able and willing to give written, informed consent

Exclusion Criteria:

  • Comorbidities: diseases of hematology or immunology system; hepatic or renal dysfunction; metabolic diseases.
  • BMI>35kg/m2
  • Life expectancy≤3mo
  • The chemotherapy treatment is palliative.
  • The patient has received radiotherapy or neoadjuvant chemotherapy prior to the operation.

Sites / Locations

  • First Affiliated Hospital, Sun Yat-sen UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Experimental

Experimental

Arm Label

EN

ENLDEPA

ENHDPEA

Arm Description

The subjects take in 150g of Nutriall per day. Oral administration of the liquid is divided into 3 times per day. The treatment lasts for 21d. During the test period patients are treated with the first course of XELOX.

The subjects take in the same dose of Nutriall for the same duration as those in EN group. In addition, they take in 3 grams of EPA per day during the 21 days of treatment. The patients are treated with the first course of XELOX.

The subjects take in the same dose of supportan for the same duration as those in EN group. In addition, they take in 6 grams of EPA per day during the 21 days of treatment. The patients are treated with the first course of XELOX.

Outcomes

Primary Outcome Measures

Serum level of proalbumin

Secondary Outcome Measures

Weight in light clothing
Height and BMI
mid upper arm circumference and triceps skinfold thickness
Fat ratio and fat mass
Fat-free mass, muscle mass and muscle function
CD distribution of T cells
Serum level of different types of immunoglobulin
Serum level of different types of cytokines
Serum level of Cortisol
Serum level of transferrin
Serum level of ALT and AST
Serum level of creatine and BUN
Serum level of total triglyceride, total cholesterol, LDL, HDL
Records of EPA intake
Records of chemotherapy-associated side effects
Serum level of albumin
Serum level of CEA, CA125, CA199
Records of Nutriall intake
Records of food intake

Full Information

First Posted
January 12, 2010
Last Updated
October 4, 2011
Sponsor
Sun Yat-sen University
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1. Study Identification

Unique Protocol Identification Number
NCT01048463
Brief Title
Effect of Enteral Nutrition Rich in Eicosapentaenoic Acid (EPA) on Patients Receiving Chemotherapy for GI Tumor
Official Title
Phase 3 Study of Enteral Nutrition Rich in Eicosapentaenoic Acid in Patients Receiving Chemotherapy for Gastric Cancer or Colorectal Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
October 2011
Overall Recruitment Status
Unknown status
Study Start Date
December 2009 (undefined)
Primary Completion Date
December 2011 (Anticipated)
Study Completion Date
January 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sun Yat-sen University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Cancer, Colorectal Cancer, Chemotherapy
Keywords
gastric cancer, colorectal cancer, chemotherapy, eicosapentaenoic acid, enteral nutrition

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
EN
Arm Type
Placebo Comparator
Arm Description
The subjects take in 150g of Nutriall per day. Oral administration of the liquid is divided into 3 times per day. The treatment lasts for 21d. During the test period patients are treated with the first course of XELOX.
Arm Title
ENLDEPA
Arm Type
Experimental
Arm Description
The subjects take in the same dose of Nutriall for the same duration as those in EN group. In addition, they take in 3 grams of EPA per day during the 21 days of treatment. The patients are treated with the first course of XELOX.
Arm Title
ENHDPEA
Arm Type
Experimental
Arm Description
The subjects take in the same dose of supportan for the same duration as those in EN group. In addition, they take in 6 grams of EPA per day during the 21 days of treatment. The patients are treated with the first course of XELOX.
Intervention Type
Drug
Intervention Name(s)
Nutriall
Other Intervention Name(s)
Complete Enteral Nutrition Emulsion for cancer patients
Intervention Description
The subjects take in 150g of Nutriall (Produced by Guangdong Academy of Agriculture Science. Every 50 grams of nutriall contains 9.3mg of VitC and 0.8mg of VitE) per day. Oral administration of the liquid is divided into 3 times per day. The treatment lasts for 21d.
Intervention Type
Drug
Intervention Name(s)
LDEPA
Other Intervention Name(s)
Eicosapentaenoic acid
Intervention Description
The subjects take in 24 pils of EPA capsule per day. The medium is gelatine. Each capsule contains 0.125g of EPA and 0.125g of olive oil. The capsules are provided by nutritional department of our institute). The treatment lasts for 21d.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Gelatin capsule
Intervention Description
The subjects take in 24 pils of gelatin capsule (each contains 0.25g of olive oil, provided by nutritional department of our institute) per day. The treatment lasts for 21d.
Intervention Type
Drug
Intervention Name(s)
HDEPA
Other Intervention Name(s)
Eicosapentaenoic acid
Intervention Description
The subjects take in 24 pils of EPA capsule per day. The medium is gelatine. Each capsule contains 0.25g of EPA. The capsules are provided by nutritional department of our institute). The treatment lasts for 21d.
Intervention Type
Drug
Intervention Name(s)
Chemotherapy
Other Intervention Name(s)
XELOX chemotherapy
Intervention Description
Oxaliplatin 135mg/m2 d1,xeloda 1000mg/m2 d1-21. (XELOX)
Primary Outcome Measure Information:
Title
Serum level of proalbumin
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Secondary Outcome Measure Information:
Title
Weight in light clothing
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Height and BMI
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
mid upper arm circumference and triceps skinfold thickness
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Fat ratio and fat mass
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Fat-free mass, muscle mass and muscle function
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
CD distribution of T cells
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Serum level of different types of immunoglobulin
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Serum level of different types of cytokines
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Serum level of Cortisol
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Serum level of transferrin
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Serum level of ALT and AST
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Serum level of creatine and BUN
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Serum level of total triglyceride, total cholesterol, LDL, HDL
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Records of EPA intake
Time Frame
The whole experiment period
Title
Records of chemotherapy-associated side effects
Time Frame
The whole experiment period
Title
Serum level of albumin
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Serum level of CEA, CA125, CA199
Time Frame
The starting and ending day of the experiment for a certain subject (day1 and day21)
Title
Records of Nutriall intake
Time Frame
The whole experiment period
Title
Records of food intake
Time Frame
The middle 3 days of the whole experiment period (day10, day11, day12)

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The cases have undergone radical excision on gastric cancer or colorectal cancer. Without contraindication for chemotherapy. Eligible for postoperative adjuvant XELOX chemotherapy. Capable of taking in food or drug orally. Without severe absorption dysfunction Able and willing to give written, informed consent Exclusion Criteria: Comorbidities: diseases of hematology or immunology system; hepatic or renal dysfunction; metabolic diseases. BMI>35kg/m2 Life expectancy≤3mo The chemotherapy treatment is palliative. The patient has received radiotherapy or neoadjuvant chemotherapy prior to the operation.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shi Fang, MD
Phone
86-0-13539951951
Email
fangshi2008@yahoo.com.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Hanping Shi, MD, PhD
Phone
86-0-13802741263
Email
shihp38@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Huilian Zhu, MD
Organizational Affiliation
Sun Yat-sen University
Official's Role
Study Director
Facility Information:
Facility Name
First Affiliated Hospital, Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510080
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Han-ping Shi, MD, PhD
Phone
86-0-13802741263
Email
shihp38@hotmail.com

12. IPD Sharing Statement

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Effect of Enteral Nutrition Rich in Eicosapentaenoic Acid (EPA) on Patients Receiving Chemotherapy for GI Tumor

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