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Clinical Trials in Sweden / NCT03343236
Active, not recruiting Observational

Nutrition and Inflammation in Patients With Head and Neck Cancer

NCT03343236 · tracked via the Priya Life Science Sweden tracker
Phase
Observational
Started
2015-11-01
Last updated
2024-12-13

Condition(s) studied

Head and Neck NeoplasmsRadiotherapy Side EffectInflammationMetabolism

Investigational drug(s) / intervention(s)

Radiotherapy

Radiotherapy: All patients will undergo radiotherapy or surgery, or combined modality treatment

Study summary

An estimated 1500 people in Sweden will annually be diagnosed with head and neck cancer (HNC). Five year survival is approximately 69%. Long-term sequelae are common and in particular nutritional problems and fatigue. Radiotherapy (RT) is the cornerstone of treatment, either as single modality treatment or combined modality treatment. RT can induce immune responses at the site of tumor. It has been demonstrated that RT can lead to a strong systemic immune response . We have previously shown that an increase of conventional measures of systemic immune response to RT varied significantly across individuals. We predict that local immune response plays a major role in the antitumor effect. We also predict that a strong systemic immune response contributes to malnutrition and influence on survival. And malnutrition may lead to a worse response to RT.

The overall aim of this multicenter observational longitudinal study is to prospectively identify immunological and metabolic variables that affect the outcome of HNC patients. We will systematically investigate the local and systemic immune response induced by RT as well as explore alterations in metabolite composition induced by disease and treatment through global metabolite profiling. A platform for studies on immuno-metabolic changes in HNC patients has been established in the Uppsala-Orebro and Northern regions. Approximately 370 patients per year are eligible. Findings in this study can have implications on the development of personalized therapy in patients with HNC. The long-term benefit of the study will be the identification of measures for improved patient surveillance in order to improve the general and nutritional outcomes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Patients with newly diagnosed head and neck cancer Exclusion Criteria: Previous treatment for malignant disease except for skin cancer, severe alcohol abuse, psychiatric disorder, inability to understand Swedish

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Otolaryngology, Head & Neck Surgery, Uppsala University Hospital Uppsala Sweden

More Uppsala University trials in Sweden

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03343236 on ClinicalTrials.gov ↗ ← All trials in Sweden