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The Association of hsCRP and Radiotherapy-Induced Toxicity in Patients With Nasopharyngeal Carcinoma

An Explorative Study on the Association of High Sensitivity C-Reactive Protein (hsCRP) and Radiotherapy-Induced Toxicity in Patients With Nasopharyngeal Carcinoma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04303975
Enrollment
300
Registered
2020-03-11
Start date
2021-06-30
Completion date
2021-12-31
Last updated
2020-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nasopharyngeal Carcinoma, Head and Neck Cancer, Toxicity Due to Radiotherapy

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

Jiarong Chen, MD
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years

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

MeasureTime frameDescription
Incidence of adverse eventsThrough treatments completion,12 weeksAll adverse events were recorded during treatment(for example, oral mucositis, dermatitis).
hsCRP levelsThrough treatments completion,12 weeksThe 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

Contacts

Primary ContactJiarong Chen, PhD
garwingchan@163.com86-0750-3399003
Backup ContactYanghao Ruan
ruanyanghao@126.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026