Nutritional Supplementation in Head and Neck Cancers

Undernutrition Clinical Trial

Official title:

A Randomized Open Label Trial of Multimodal Oral Nutritional Supplementation Versus Standard Care, to Prevent / Attenuate Malnutrition in Patients With Cancers of the Head and Neck Receiving (Chemo)-Radiotherapy Treatment.

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05379712
• Other study ID #: IIT-0024
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: July 2024
• Est. completion date: October 2025

Study information

• Verified date: January 2024
• Source: AHS Cancer Control Alberta
• Contact: Vickie Baracos
• Phone: 780-432-8232
• Email: Vickie.Baracos[@]albertahealthservices.ca
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether multimodal nutrition therapy (primary nutrition intervention + adjuvant nutrition therapy) will support patients to optimize their total caloric intake during cancer treatment by measuring the difference in mean cumulative energy intake between the intervention and control group over the duration of cancer treatment.

Description:

This will be an randomized, open label, parallel assignment study during cancer treatment (Baseline - Week 7 for Primary endpoint) comparing multimodal oral nutrition therapy versus standard care. Starting at Week 8, all patients receive the intervention arm until study ends at Week 14. Patients in the intervention arm continue the intervention, patients on the standard care arm cross over to the intervention (deferred nutrition intervention).

The primary objective is to assess a multimodal nutrition therapy with two Medical Foods (primary nutrition intervention+ adjuvant nutrition therapy) with features adapted for patients with cancers of the head and neck receiving chemo-radiotherapy treatment, to maintain oral dietary intake during treatment.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 81
• Est. completion date: October 2025
• Est. primary completion date: October 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients must have the ability to read, understand, and sign an informed consent and must be willing to comply with study treatment and follow-up.

2. Male or female

3. =18 years of age

4. Histopathologically confirmed primary squamous cell carcinoma of the oral cavity and oropharynx, larynx or hypopharynx, who have agreed to receive radical intent radiotherapy as primary treatment or adjuvant treatment post-surgery, with or without platinum chemotherapy

5. Capable of volitional oral nutritional intake at baseline.

6. A diagnostic CT image taken with a maximum of 30 days before initiation of radical intent radiotherapy. If the CT scan history in the patient's clinical record does not include a study within this window, a baseline non-contrast enhanced CT abdomen will be conducted.

7. An Eastern Cooperative Oncology Group Performance Status of = 2

Exclusion Criteria:

1. Fed by nasogastric tube, gastrostomy or total parenteral nutrition

2. Cancer of the nasopharynx, thyroid or salivary gland

3. Life expectancy <6 months.

4. A known hypersensitivity / allergy to the investigational product or to any ingredient in their formulations (e.g. Milk/Lactose, Fish).

5. Enrolment in any other clinical protocol or investigational study with an interventional agent or assessments that may interfere with study procedures.

6. Patients with untreated brain metastases (patients with previously resected and/or radiated brain metastases without neurologic symptoms are permitted).

7. Poorly controlled chronic illnesses or other inflammatory diseases (e.g. COPD, uncontrolled non-insulin dependent diabetes, rheumatoid arthritis).

8. In the investigators' opinion, patients who have medical conditions that could interfere with nutrient metabolism or absorption (e.g., short bowel syndrome, Crohn's disease, etc.)

Related Conditions & MeSH terms

• Malnourishment
• Malnutrition
• Nutritional Deficiency
• Undernutrition

Intervention

Other:
• Resource® Support Plus
Nestlé Resource Support Plus® is a high energy- and protein-density Medical Food enriched with omega 3 polyunsaturated fatty acids. This is a nutritionally complete formula, in an easy to swallow, palatable, concentrated low volume, available in 2 flavours optimized for cancer patients undergoing chemotherapy and/or radiation in taste tests. It provides in a 125 mL serving: 250 kcal, 11.5 g protein and 0.95g of omega-3 fatty acid (eicosapentaenoic acid, EPA).

Locations

Country	Name	City	State
Canada	Cross Cancer Institute	Edmonton	Alberta

Sponsors (1)

Lead Sponsor	Collaborator
AHS Cancer Control Alberta

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in mean cumulative energy intake	Energy intake is calculated from a one-day diet record in which the patient lists the identity and quantity of all foods and beverages consumed in the designated 24 hour time period at the end of each week (Baseline - Week 14).	Up to 14 weeks
Secondary	Change in mean cumulative protein take	Energy intake is calculated from a one-day diet record in which the patient lists the identity and quantity of all foods and beverages consumed in the designated 24 hour time period at the end of each week (Baseline - Week 14)	Up to 14 Weeks
Secondary	Change in body weight (kg)	Change in weight (kg) from the previous week.	Baseline-Week 14
Secondary	Change in Nutritional blood biomarkers	A sample of blood will be collected for albumin, absolute neutrophil count, lymphocyte count, C-reactive protein, standard complete blood count-differential White Blood cell count and to measure serum CRP and albumin	Baseline measures will be compared to levels at weeks 7 and 14
Secondary	Head and Neck Symptom Checklist	A survey tool for HNC patient self-assessment of the presence and degree of interference with eating, over the past 3 days, of 17 symptoms known to impact dietary intake. Scores range from 34 to 170 pts, where higher scores reflect a greater presence and interference with eating. Completed at weeks 0, 4, 7, 11, 14	Up to 14 weeks
Secondary	Taste and smell survey	A survey tool for patient self-assessment of the presence, characterization and severity of taste and smell alterations. This tool yields a 'chemosensory complaint score' of up to 16 (greatest severity of taste and smell alterations). Completed at weeks 0, 4, 7, 11, 14.	Up to 14 weeks
Secondary	Medication use for pain	Use of pain medication will be captured weekly by a one- day pain medication log.	Up to 14 weeks
Secondary	Percent oral intake from oral nutritional supplements	The volume (mL) of study products consumed will be determined from the weekly one-day diet record.	Up to 14 weeks
Secondary	Product Sensory Assessment questionnaire	A product evaluation form for the Medical Nutrition products will be used to evaluate product overall sensory assessment, including acceptance and perception of characteristic product attributes that influence overall sensory acceptance. Medical Nutrition sensory acceptance will be evaluated by "overall liking" on the 9-point hedonic scale (1= dislike extremely; 9 = like extremely). Completed at weeks 0, 2, 4, 6, 8, 10, 12, 14.	Up to 14 weeks
Secondary	Functional Assessment of Anorexia-Cachexia Treatment (FAACT) 5 Question Anorexia/Cachexia subscale (AC/S)	The FAACT is a validated Quality of Life Scale to capture patient experience of cancer related cachexia - anorexia. Completed at weeks 0, 4, 7,11, 14	Up to 14 weeks
Secondary	Cumulative energy intake (kcal/kg BW)	Energy intake is calculated from a one-day diet record in which the patient lists the identity and quantity of all foods and beverages consumed in the designated 24 hour time period at the end of each week (Baseline - Week 14)	Up to 14 weeks
Secondary	Cumulative protein take (g pro/kg BW)	Protein intake is calculated from a one-day diet record in which the patient lists the identity and quantity of all foods and beverages consumed in the designated 24 hour time period at the end of each week (Baseline - Week 14)	Up to 14 weeks
Secondary	Change in computed-tomography (CT) defined skeletal muscle and fat mass)	Imaging for body composition (muscle, fat)	Within 30 days prior to start of treatment, Week 14
Secondary	Tertiary hospital admission	Review of patient medical records for instances of hospitalization with date(s) of admission falling between baseline and week 14 of study.	Up to 14 weeks