West China Hospital, Sichuan University
Chengdu, Sichuan, China
NCT Number: NCT07029373
This prospective study investigates the dynamic changes in plasma calcitonin gene-related peptide (CGRP) levels during radiotherapy and their association with radiotherapy-related pain in patients with head and neck malignancies.
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Notify Me18 year and older
All sexes
Observational
Chengdu, Sichuan, China
Radiotherapy-related pain is a major clinical challenge that significantly affects the long-term quality of life and treatment adherence of patients with head and neck cancer. Current analgesic strategies offer limited efficacy, and reliable biomarkers for predicting pain risk are lacking. In recent years, calcitonin gene-related peptide (CGRP) has drawn increasing attention for its critical role in chronic pain regulation, as demonstrated in various pain models. However, no systematic studies have yet investigated the expression patterns and clinical relevance of CGRP in radiotherapy-induced pain among patients with head and neck malignancies. This single-center, prospective observational study aims to enroll patients with head and neck cancer receiving either definitive or postoperative adjuvant radiotherapy. Plasma samples will be collected before, during, and after radiotherapy for measurement of CGRP levels. Pain intensity will be simultaneously assessed using the Numeric Rating Scale (NRS) and the Brief Pain Inventory-Short Form (BPI-SF). The study seeks to explore the dynamic changes in plasma CGRP levels throughout the radiotherapy course and to analyze their correlation with patient-reported pain, thereby providing potential insights into biomarker-based pain prediction and management strategies in this patient population.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Histologically confirmed head and neck malignancy
Planned to receive definitive or postoperative adjuvant radiotherapy
Radiotherapy duration ≥ 4 weeks, with irradiation field involving the oral cavity, pharynx, or neck region
Able and willing to provide written informed consent
Able to complete pain assessments and blood sample collection
Exclusion criteria
Presence of uncontrolled hypertension, diabetes, or migraines
Presence of other active malignancies or major systemic diseases (e.g., severe hepatic or renal dysfunction)
Currently receiving or recently received treatments that may significantly affect pain perception (e.g., opioids, antidepressants)
Pregnant or breastfeeding
Inability to complete follow-up or poor treatment compliance
Time frame: Baseline (prior to the initiation of radiotherapy), At the end of the third week of radiotherapy (approximately 21±2 days after the 15th radiotherapy session), Within one week after the completion of radiotherapy.
To assess dynamic changes in CGRP levels during the course of radiotherapy.
Time frame: Baseline (prior to the initiation of radiotherapy), At the end of the third week of radiotherapy (approximately 21±2 days after the 15th radiotherapy session), Within one week after the completion of radiotherapy.
To evaluate the association between CGRP expression and radiotherapy-induced pain.
West China Hospital
Other
A Prospective Clinical Study for Analyzing Plasma Calcitonin Gene-Related Peptide (CGRP) Levels in Patients With Head and Neck Malignancies Undergoing Radiotherapy
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