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Early and Whole Course Nutritional Support by Nutren® Optimum During IMRT for Nasopharyngeal Carcinoma

Primary Purpose

Nasopharyngeal Carcinoma, Nutritional Support

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Radiotherapy
Chemotherapy
Nutren® Optimum
Sponsored by
Sun Yat-sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nasopharyngeal Carcinoma focused on measuring nasopharyngeal carcinoma, nutritional support, early and whole course, efficacy and safety

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Pathologically confirmed and previously untreated nasopharyngeal carcinoma without distant metastasis.
  • Age ≥ 18 years and < 65 years.
  • Karnofsky performance status (KPS) score ≥ 70.
  • Planned to receive radiotherapy alone or concurrent chemoradiotherapy, with intensity-modulated radiation therapy (IMRT).
  • Adequate normal organ function.
  • Well nutritional status, with PG-SGA≤1 score and NRS2002<3 scores.
  • Without other severe diseases.
  • Signed informed consent voluntarily, and could complete required oral nutrition, questionnaire survey and follow-up.

Exclusion Criteria:

  • Known allergic reaction to any component of Nutren® Optimum, or severe allergic constitution.
  • Poor compliance.
  • Other conditions that the investigators consider as inappropriate for enrolling into this study.

Sites / Locations

  • Department of Radiation Oncology, Sun Yat-Sen University Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental Group

Controlled Group

Arm Description

The patients in the Experimental Group are allocated to receive radical radiotherapy with or without chemotherapy plus Nutren® Optimum of 7 scoops tid at begin of radiotherapy.

The patients in the Controlled Group are allocated to receive radical radiotherapy with or without chemotherapy plus routine diet guidance at begin of radiotherapy.

Outcomes

Primary Outcome Measures

Decline in nutritional status needed upgrading nutritional intervention
The percentage of patients whose body weight decreased by 5% over baseline, or the PG-SGA score was more than 8, or the NRS2002 score was more than 3.

Secondary Outcome Measures

Quality of life
The standard scores assessed by EORTC QOL scale decreased by more than 10 points
Moderate and severe bone marrow depression and anemia
Incidence of 3-4 degrees bone marrow depression and anemia according to CTCAE (version 4)
Severe oral mucositis
Incidence of 3-4 degrees oral mucositis according to CTCAE (version 4)
Interruption rate of radiotherapy and/or chemotherapy caused by intolerance
The percentage of patients whose radiotherapy and/or chemotherapy were interrupted by treatment-related toxicity intolerance
Complete remission
The percentage of patients whose all the target lesions disappeared, no new lesions appeared according to RECIST

Full Information

First Posted
October 25, 2017
Last Updated
December 21, 2017
Sponsor
Sun Yat-sen University
Collaborators
Nestle Health Science
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1. Study Identification

Unique Protocol Identification Number
NCT03344068
Brief Title
Early and Whole Course Nutritional Support by Nutren® Optimum During IMRT for Nasopharyngeal Carcinoma
Official Title
A Single Center, Open-label, Randomized Controlled Clinical Trial on the Early and Whole Course Nutritional Support by Nutren® Optimum During Intensity Modulated Radiation Therapy for Nasopharyngeal Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2018 (Anticipated)
Primary Completion Date
December 31, 2020 (Anticipated)
Study Completion Date
March 31, 2021 (Anticipated)

3. Sponsor/Collaborators

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

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Radiation therapy remains the principal treatment for nasopharyngeal carcinoma (NPC). The most frequently occurred radiation-related side effect is probably the radiation-induced oral mucositis, which affects up to 100% of NPC patients receiving radiation therapy, especially combined with chemotherapy. Significant weight loss caused by Oral mucositis will keep patients in worse nutrition status and then to decline immune function, hematopoietic function and repair function, which will influence the patient's quality of life, reduce the tolerance of treatment, and affect treatment effect. At present, the guidelines at home and abroad more and more emphasize that early nutrition treatment and intervention before systemic malnutrition, also suggest nutrition treatment and intervention at the same time of anti-tumor treatment. First choice of nutritional intervention is oral nutrition supplement. Nutren® Optimum has a higher protein ratio and 50% of the protein sources were lactalbumin and 50% casein. Lactalbumin is a high-quality protein, with the highest nutritional value among a variety of proteins. A cup of 210ml's Nutren® Optimum contains 5g lactalbumin. Nutren® Optimum also contains dietary fiber, vitamin E, monounsaturated fat, L-carnitine, 30 kinds of vitamins and minerals and other nutrients, which can provide a comprehensive and balanced nutrition. This single center, open-label, randomized controlled clinical trial selects Nutren® Optimum as oral nutritional support for interventional group while routine diet guidance for control group, aiming to evaluate the efficacy and safety of early and whole course nutritional support by Nutren® Optimum during intensity modulated radiation therapy for nasopharyngeal carcinoma which can improve patients' nutritional state and quality of life, reduce side effects and improve the tolerability and effectiveness of antitumor treatment.
Detailed Description
Radiation therapy remains the principal treatment for nasopharyngeal carcinoma (NPC). The most frequently occurred radiation-related side effect is probably the radiation-induced oral mucositis, which affects up to 100% of NPC patients receiving radiation therapy, especially combined with chemotherapy. Oral mucositis is just the most common cause of significant weight loss for patients with nasopharyngeal carcinoma during treatment. Patients with oral mucositis will have restriction of normal food, and alternative to semi liquid or liquid diet, resulting in inadequate nutritional intake, malnutrition, weight loss. Furthermore, worse nutrition status will decline immune function, hematopoietic function and repair function, which will influence the patient's quality of life, reduce the tolerance of treatment, and affect treatment effect. At present, the guidelines at home and abroad more and more emphasize that early nutrition treatment and intervention before systemic malnutrition, also suggest nutrition treatment and intervention at the same time of anti-tumor treatment. Therefore, the timing of nutritional intervention changes from ineffective antitumor therapy as a palliative treatment to the early start of antitumor therapy. For nasopharyngeal carcinoma, early and whole course nutritional intervention can prevent and treat malnutrition or cachexia; improve the treatment tolerance and compliance; control or improve certain adverse reactions of radiotherapy; improve the quality of life; and then improve the function and curative effect. First choice of nutritional intervention is oral nutrition supplement. For patients without gastrointestinal dysfunction, parenteral nutrition is not necessary, even harmful, increasing the risk of infection. Nutren® Optimum has a higher protein ratio (P:F:C = 17:35:48), and 50% of the protein sources were lactalbumin and 50% casein. Lactalbumin is a high-quality protein, which dissolved and dispersed in the whey protein. Lactalbumin is easy digestion and absorption, with high bioavailability, and net protein utilization rate (NPU) is higher than that of casein and soy protein. Lactalbumin is rich in branched chain amino acids, which can be used as energy material for energy. Lactalbumin has a sulfur-containing amino acid, which can maintain the level of GSH and be in the role of antioxidation; containing glutamine, which contributes to muscle glycogen update and improves immune function. In addition, lactalbumin can also significantly reduce neutrophil apoptosis, enhance neutrophil migration and phagocytosis, and enhance the immune function. Therefore, lactalbumin has the highest nutritional value among a variety of proteins, known as protein king. A cup of 210ml's Nutren® Optimum contains 5g lactalbumin. Nutren® Optimum contains dietary fiber, which produces short chain fatty acids to promote the proliferation of intestinal probiotics, and play anti-inflammatory, pro-apoptotic, anti-tumor effect, and maintain intestinal health. At the same time, vitamin E is specially added in Nutren® Optimum to protect T lymphocytes, protect red blood cells, anti-oxidation, inhibit platelet aggregation, enhance immunity, and so on. In addition, 64% fat sources of Nutren® Optimum are monounsaturated fat, which conducive to the metabolism of glucose and lipid. Especially added L-carnitine can promote fat oxidation by using better fat for energy, without reducing water and muscle. Nutren® Optimum provides 30 kinds of vitamins and minerals and other nutrients, and can provide a comprehensive and balanced nutrition. This single center, open-label, randomized controlled clinical trial selects Nutren® Optimum as oral nutritional support for interventional group while routine diet guidance for control group, aiming to evaluate the efficacy and safety of early and whole course nutritional support by Nutren® Optimum during intensity modulated radiation therapy for nasopharyngeal carcinoma, which can improve patients' nutritional state and quality of life, reduce side effects and improve the tolerability and effectiveness of antitumor treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nasopharyngeal Carcinoma, Nutritional Support
Keywords
nasopharyngeal carcinoma, nutritional support, early and whole course, efficacy and safety

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Model Description
The patients eligible are divided randomly. All the patients will receive radical radiotherapy with or without chemotherapy. The cases in the Experimental Group will receive Nutren® Optimum of 7 scoops tid at begin of radiotherapy.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
408 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental Group
Arm Type
Experimental
Arm Description
The patients in the Experimental Group are allocated to receive radical radiotherapy with or without chemotherapy plus Nutren® Optimum of 7 scoops tid at begin of radiotherapy.
Arm Title
Controlled Group
Arm Type
Active Comparator
Arm Description
The patients in the Controlled Group are allocated to receive radical radiotherapy with or without chemotherapy plus routine diet guidance at begin of radiotherapy.
Intervention Type
Radiation
Intervention Name(s)
Radiotherapy
Intervention Description
Intensity Modulated Radiation Therapy, Dose: GTVnx 6810cGy/30Fr, GTVnd 6400-6600cGy/30Fr, CTV1 6000cGy, CTV2 5400cGy.
Intervention Type
Drug
Intervention Name(s)
Chemotherapy
Intervention Description
Nedaplatin 80mg/m2 d1+5-fluouracil 500mg/m2 d2-5, every 3 weeks; a total of 2-3 cycles.
Intervention Type
Dietary Supplement
Intervention Name(s)
Nutren® Optimum
Intervention Description
Nutren® Optimum, 7 scoops each time, three times a day, at begin of radiotherapy
Primary Outcome Measure Information:
Title
Decline in nutritional status needed upgrading nutritional intervention
Description
The percentage of patients whose body weight decreased by 5% over baseline, or the PG-SGA score was more than 8, or the NRS2002 score was more than 3.
Time Frame
3 months after radiotherapy
Secondary Outcome Measure Information:
Title
Quality of life
Description
The standard scores assessed by EORTC QOL scale decreased by more than 10 points
Time Frame
3 months after radiotherapy
Title
Moderate and severe bone marrow depression and anemia
Description
Incidence of 3-4 degrees bone marrow depression and anemia according to CTCAE (version 4)
Time Frame
3 months after radiotherapy
Title
Severe oral mucositis
Description
Incidence of 3-4 degrees oral mucositis according to CTCAE (version 4)
Time Frame
3 months after radiotherapy
Title
Interruption rate of radiotherapy and/or chemotherapy caused by intolerance
Description
The percentage of patients whose radiotherapy and/or chemotherapy were interrupted by treatment-related toxicity intolerance
Time Frame
3 months after radiotherapy
Title
Complete remission
Description
The percentage of patients whose all the target lesions disappeared, no new lesions appeared according to RECIST
Time Frame
3 months after radiotherapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pathologically confirmed and previously untreated nasopharyngeal carcinoma without distant metastasis. Age ≥ 18 years and < 65 years. Karnofsky performance status (KPS) score ≥ 70. Planned to receive radiotherapy alone or concurrent chemoradiotherapy, with intensity-modulated radiation therapy (IMRT). Adequate normal organ function. Well nutritional status, with PG-SGA≤1 score and NRS2002<3 scores. Without other severe diseases. Signed informed consent voluntarily, and could complete required oral nutrition, questionnaire survey and follow-up. Exclusion Criteria: Known allergic reaction to any component of Nutren® Optimum, or severe allergic constitution. Poor compliance. Other conditions that the investigators consider as inappropriate for enrolling into this study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yun-fei Xia, M.D
Phone
86-13602805461
Email
xiayf@sysucc.org.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Chen Chen, M.D
Phone
86-13570487011
Email
chenchen@sysucc.org.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yun-fei Xia, M.D
Organizational Affiliation
Sun Yat-sen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Radiation Oncology, Sun Yat-Sen University Cancer Center
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510060
Country
China

12. IPD Sharing Statement

Learn more about this trial

Early and Whole Course Nutritional Support by Nutren® Optimum During IMRT for Nasopharyngeal Carcinoma

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