Nutritional Status Assessment in Head and Neck Cancer Patients Receiving Radiotherapy or Chemo-radiotherapy (NUTRINECK)
Primary Purpose
Head and Neck Cancer
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
weekly assessment of patient's weight
Sponsored by
About this trial
This is an interventional other trial for Head and Neck Cancer focused on measuring Nutrition, Head and Neck Cancer
Eligibility Criteria
Inclusion Criteria:
- Males or females older than 18 years
- Performance Status 0 or 1 or 2
- Locally advanced head and neck cancer treated with a curative intent treatment consisting of either concomitant chemo-radiotherapy or adjuvant radiation therapy or adjuvant chemo-radiotherapy.
- Signed Informed Consent
Exclusion Criteria:
- Other cancer or previous cancer within 2 years or evolutive cancer
- Performance Status 3 or 4
- NGT or PEG at screening period
- Any legal, social, psychological reasons that could jeopardize the patient's compliance to the study constrains.
Sites / Locations
- Centre Henri Becquerel
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Nutrition state determination
Arm Description
Determination of nutritional state and inflammatory status: weekly assessment of patient's weight biological parameters (albumin, transthyretin, orosomucoid) and weekly assessment of patient's weight
Outcomes
Primary Outcome Measures
weight
Measure of weight ( in Kg)
Secondary Outcome Measures
Nutritional status determination
Determination of nutritional status by assessing albuminemia
Nutritional status determination
Determination of nutritional status by assessing transthyretin
Nutritional status determination
Determination of nutritional status by assessing albuminemia
Nutritional status determination
Determination of nutritional status by assessing transthyretin
Nutritional status determination
Determination of nutritional status by assessing albuminemia
Nutritional status determination
Determination of nutritional status by assessing transthyretin
Inflammatory status
Determination of inflammatory status by assessing orosomucoid
Inflammatory status
Determination of inflammatory status by assessing CRP
Inflammatory status
Determination of inflammatory status by assessing orosomucoid
Inflammatory status
Determination of inflammatory status by assessing CRP
Inflammatory status
Determination of inflammatory status by assessing orosomucoid
Inflammatory status
Determination of inflammatory status by assessing CRP
BMI calculation
Calculation of BMI using height and weight
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02900963
Brief Title
Nutritional Status Assessment in Head and Neck Cancer Patients Receiving Radiotherapy or Chemo-radiotherapy
Acronym
NUTRINECK
Official Title
Nutritional Assessment of Locally Advanced Head and Neck Cancer Patients Who Underwent Exclusive or Adjuvant Radiotherapy or Chemo-radiotherapy
Study Type
Interventional
2. Study Status
Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
April 2014 (undefined)
Primary Completion Date
August 2018 (Actual)
Study Completion Date
December 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Henri Becquerel
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Radiotherapy and chemotherapy are standard treatment of head and neck cancer alone or associated to surgical treatment. Early (during treatment or the following weeks) and late side effects contribute to malnutrition in this population at risk. In this context, nutritional support adapted by dietary monitoring and enteral nutrition (nasogastric tube or gastrostomy) are often necessary. The early identification of the patients with high malnutrition risk and requiring enteral nutrition is necessary to improve the tolerance and efficacy of treatment. This prospective study research the factors of malnutrition during head and neck radiotherapy.
Detailed Description
Head and neck cancer is one of the most common malignancies in the world, Malnutrition occurs frequently at the time of diagnosis as consequences of alcohol consumption and tobacco use that is quite common in this patients population, and of local tumor invasion, obstructing the function of swallowing and chewing. In addition, during the treatment, mucositis, anorexia, dysphagia, mouth sores, and other acute and late toxic effects of radiotherapy (RT) and chemotherapy frequently worsen the nutritional status.
Poor nutritional status and chemotherapy or RT-toxicity, lead to treatment interruption frequently and is also associated with higher risk of infection, hospital readmission, early death, worse survival outcomes, and deterioration in the quality of life (QoL). According to published results, one third of the patient would have benefit from a complete treatment. In addition, the correlation exists between some biological parameters (CRP, albumin, neutrophils, Hb) and the nutritional status. Therefore, it deems essential to maintain nutritional status in head and neck cancer patients undergoing RT and chemotherapy.
Dietary counseling and oral supplements showed positive influences on nutritional outcomes and QoL However, their role is limited when it comes to obstruction or mucositis. Thus, enteral feeding may be a choice either through nasogastric tube (NGT) or percutaneous endoscopic gastrostomy (PEG). Studies investigated the effects of PEG compared with NGT were not conclusive or showing no consistent results on nutritional status, treatment interruption, nutrition-related hospital admission, and tube-related complications in the head and neck cancer patients receiving RT or chemo-radiotherapy.
The optimal method and the timing of placement are still debated. Consequently, the aim of this study is to collect data on our current daily practice on supplementary nutrition method ( NGT, PEG) in head and neck cancers patients treated in our radiation therapy unit and to identify factors predicting good treatment outcomes( ie full treatment administration).
Secondary objectives are to collect nutritional data during the treatment, to study the nutritional status in relation to acute or late adverse events, to study the impact of an early enteral feeding on clinical and biological parameters.
Ancillary study: Sarco-Nutrineck The aim of this ancillary study is to collect data on prevalence of low muscle mass in this population, treatment outcomes and survival.
Study measures:
At baseline: body height and weight, calculated BMI. Biological parameters: albumin, orosomucoid, transthyretin, CRP Daily - during the treatment period: weight Weekly - during the treatment period: albumin, orosomucoid, transthyretin, CRP. The Nutritional and inflammatory status score will be calculated.
Clinical criteria on the requirement of enteral nutrition (or need for artificial nutrition) in case of weight loss persisting at least for three days during radiotherapy:
The aim of this study is to investigate whether nutritional screening on admission can be used to determine risk levels for adverse clinical events and treatment outcome ( full treatment administration) in head and neck cancer and to propose a risk stratification based on nutritional screening before radiotherapy or concomitant chemo radiotherapy.
tube (NGT) will be placed according to the following procedure: The weight will be assessed on daily basis and will be compared to the figure at baseline, before treatment. If the weight loss is superior to 2 kg, the patient will consult a radiotherapist who will perform a physical examination, a nutritional assessment (history, appetite change, taste, quantity and quality of oral food intake, medication, details regarding weight change and BMI). In addition to dietary counselling and oral supplementation, If indicated, analgesic drugs and or treatment of associated mucositis will be prescribed.
In case of persisting weight loss or severe dysphagia or no oral solid food intake, a nasogastric tube (NGT) will be placed by a nurse and a personalized nutritional counselling by a dietician will be organized.
Biological exams will be done according to our local practice and standard, and the results will be analyzed to assess the safety. Regular clinical exams will be realized. All adverse events will reported according to the common terminology criteria for adverse events scale.
Follow-up period. The patients will benefit from a clinical exam, height, weight, BMI, biological exam (including albumin, orosomucoid, transthyretin, CRP) one month after the end of the treatment, and then at three months and at twelve months, late toxicities will be recorded.
The aim of this study is to investigate whether nutritional screening on admission can be used to determine risk levels for adverse clinical events and treatment outcome (full treatment administration) in head and neck cancer and to propose i) isk stratification based on nutritional screening before radiotherapy or concomitant chemo radiotherapy ii) decisional algorithm on placement of a NGT
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Head and Neck Cancer
Keywords
Nutrition, Head and Neck Cancer
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
280 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Nutrition state determination
Arm Type
Other
Arm Description
Determination of nutritional state and inflammatory status:
weekly assessment of patient's weight biological parameters (albumin, transthyretin, orosomucoid) and weekly assessment of patient's weight
Intervention Type
Other
Intervention Name(s)
weekly assessment of patient's weight
Intervention Description
Biological assessment to determine biological and inflammatory status Quality of life questionary
Primary Outcome Measure Information:
Title
weight
Description
Measure of weight ( in Kg)
Time Frame
one year
Secondary Outcome Measure Information:
Title
Nutritional status determination
Description
Determination of nutritional status by assessing albuminemia
Time Frame
3 months
Title
Nutritional status determination
Description
Determination of nutritional status by assessing transthyretin
Time Frame
3 months
Title
Nutritional status determination
Description
Determination of nutritional status by assessing albuminemia
Time Frame
6 months
Title
Nutritional status determination
Description
Determination of nutritional status by assessing transthyretin
Time Frame
6 months
Title
Nutritional status determination
Description
Determination of nutritional status by assessing albuminemia
Time Frame
One year
Title
Nutritional status determination
Description
Determination of nutritional status by assessing transthyretin
Time Frame
One year
Title
Inflammatory status
Description
Determination of inflammatory status by assessing orosomucoid
Time Frame
3 months
Title
Inflammatory status
Description
Determination of inflammatory status by assessing CRP
Time Frame
3 months
Title
Inflammatory status
Description
Determination of inflammatory status by assessing orosomucoid
Time Frame
6 months
Title
Inflammatory status
Description
Determination of inflammatory status by assessing CRP
Time Frame
6 months
Title
Inflammatory status
Description
Determination of inflammatory status by assessing orosomucoid
Time Frame
one year
Title
Inflammatory status
Description
Determination of inflammatory status by assessing CRP
Time Frame
one year
Title
BMI calculation
Description
Calculation of BMI using height and weight
Time Frame
one year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Males or females older than 18 years
Performance Status 0 or 1 or 2
Locally advanced head and neck cancer treated with a curative intent treatment consisting of either concomitant chemo-radiotherapy or adjuvant radiation therapy or adjuvant chemo-radiotherapy.
Signed Informed Consent
Exclusion Criteria:
Other cancer or previous cancer within 2 years or evolutive cancer
Performance Status 3 or 4
NGT or PEG at screening period
Any legal, social, psychological reasons that could jeopardize the patient's compliance to the study constrains.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sebastien Thureau, MD
Organizational Affiliation
Centre Henri Becquerel
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Henri Becquerel
City
Rouen
ZIP/Postal Code
76038
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Nutritional Status Assessment in Head and Neck Cancer Patients Receiving Radiotherapy or Chemo-radiotherapy
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