Nasopharyngeal Carcinoma, Head and Neck Cancer, Toxicity Due to Radiotherapy
Conditions
Brief summary
The primary purpose of this study is to explore the association of high sensitivity C-reactive protein (hsCRP) and radiotherapy(RT)-induced toxicity in patients with nasopharyngeal carcinoma. In each patient, hsCRP levels in the pre- and post-RT plasma samples will be measured according to the schedule we set.
Interventions
Only clinical parameters were recorded, no intervention was made.
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients were pathologically newly diagnosed with nasopharyngeal carcinoma and had no previous history of other tumors * According to the treatment strategies of doctors, patients need to receive radiotherapy with or without chemotherapy (for example, neoadjuvant chemotherapy, concurrent chemotherapy, adjuvant chemotherapy) or targeted therapy * Willingness to sign the informed consent and return to enrolling institution for follow-up and data collection
Exclusion criteria
* Patients do not conform to the inclusion criteria * Pregnant or Nursing women * Men or women of childbearing potential who are unwilling to employ adequate contraception * Vital organs dysfunction(for example, kidneys, heart, liver, lungs, brain) * Other contraindications or unsuitable conditions for radiotherapy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of adverse events | Through treatments completion,12 weeks | All adverse events were recorded during treatment(for example, oral mucositis, dermatitis). |
| hsCRP levels | Through treatments completion,12 weeks | The hscrp levels in the plasma samples from each participant were measured at the following time points: 1. at the time of diagnosis completion/before the initiation of the first neoadjuvant chemotherapy 2. before the initiation of each neoadjuvant chemotherapy 3. before the initiation of the first radiotherapy 4. during radiotherapy, once a week 5. 1 week and 4weeks after the last radiotherapy |