Jiangsu Cancer Hospital
Nanjing, China
NCT Number: NCT05912582
This clinical research aims to explore potential biomarkers and validate molecular signatures' predictive and prognostic value in nasopharyngeal carcinoma.
Trial opening soon.
Get Notified18 year–80 year
All sexes
Observational
Nanjing, China
Primary endpoint: Evaluation of the major pathological response of nasopharyngeal carcinoma patients.
Secondary endpoint: Evaluation of failure-free survival and overall survival of nasopharyngeal carcinoma patients.
Outline: This is a prospective observational study. Patients of nasopharyngeal carcinoma undergo inductive chemotherapy and concurrent chemoradiotherapy. Whole blood is obtained from patients when recruited, completing 10, 20, 32 fractions of radiation therapy, 3 months after radiation therapy and disease progression. Tumor tissue specimens are obtained from patients when recruited and disease progression. The samples are analyzed for biomarkers and spatial transcriptomics. The biomarkers and spatial transcriptomics are correlated with clinical outcomes (major pathological response, progression-free survival, overall survival, tumor response to treatment, distant metastasis, recurrence and death).
The analysis aims to explore potential biomarkers and validate molecular signatures' predictive and prognostic value in nasopharyngeal carcinoma. This will lead to the definition of risk groups and stratification of patients and will help in precision medicine of nasopharyngeal carcinoma.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Treatment with palliative intent
Intensity modulated radiation therapy (IMRT) combined with chemotherapy
Other names: IMRT
Time frame: 3 months after radiation therapy
Time frame: 2 years after radiation therapy
Time frame: 2 years after radiation therapy
Contact information is provided by the study sponsor or research team.
Jiangsu Cancer Institute & Hospital
Other
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