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Molecular Research on Predictive Efficacy and New Therapeutic Targets for Nasopharyngeal Carcinoma

Molecular Research on Predictive Efficacy and New Therapeutic Targets for Nasopharyngeal Carcinoma Based on Tumor Immune Microenvironment

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07198802
Enrollment
600
Registered
2025-09-30
Start date
2025-10-31
Completion date
2028-12-31
Last updated
2025-09-30

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

Conditions

Nasopharyngeal Carcinoma (NPC)

Brief summary

To analyze the spatiotemporal dynamic evolution of nasopharyngeal carcinoma before and after immunotherapy and during tumor progression, 2\ 3 key cell subsets or node molecules were screened to predict the curative effect. Spatial metabolome and organoids were used to elucidate the mechanism of key factors leading to immunotherapy tolerance in NPC and identify new targets for intervention.

Interventions

OTHERNo Intervention

This project involves no therapeutic intervention for the subjects.

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 75 Years

Inclusion criteria

Before the trial, the participants must meet all of the following requirements to be eligible for inclusion. 1. Clearly diagnosed with nasopharyngeal carcinoma by pathology; 2. Patients who have received combined radiotherapy, chemotherapy and immunotherapy in our hospital; 3. Patients diagnosed in our hospital from January 2025 to December 2028; 4. Have relatively complete clinical data; 5. Age between 15 and 75 years old;

Exclusion criteria

Before the trial, the participants who meet any of the following requirements cannot be included. 1. The final diagnosis of the participants is other diseases, including lymphoma, or oropharyngeal cancer, etc.; 2. The participants failed to obtain pathological and imaging data for various reasons; 3. Due to physical conditions, they did not undergo relevant examinations, refused to accept examinations, or interrupted treatment for other reasons, and were unable to complete clinical assessment.

Design outcomes

Primary

MeasureTime frameDescription
Failure-free survival (FFS)3-yearFailure-free survival is measured from day of diagnosis until treatment failure, death from any cause, or last follow-up visit, whichever occurred first

Secondary

MeasureTime frameDescription
Overall survival (OS)5-yearOverall survival is measured from day of diagnosis until death due to any cause or the latest known date alive

Outcome results

None listed

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