Molecular Research on Predictive Efficacy and New Therapeutic Targets for Nasopharyngeal Carcinoma
1 other identifier
observational
600
0 countries
N/A
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2025
Typical duration for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 17, 2025
CompletedFirst Posted
Study publicly available on registry
September 30, 2025
CompletedStudy Start
First participant enrolled
October 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2028
September 30, 2025
September 1, 2025
3.2 years
July 17, 2025
September 22, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Failure-free survival (FFS)
Failure-free survival is measured from day of diagnosis until treatment failure, death from any cause, or last follow-up visit, whichever occurred first
3-year
Secondary Outcomes (1)
Overall survival (OS)
5-year
Study Arms (1)
Study Groups
Interventions
Eligibility Criteria
Patients with nasopharyngeal carcinoma who were admitted to our hospital
You may qualify if:
- Clearly diagnosed with nasopharyngeal carcinoma by pathology;
- Patients who have received combined radiotherapy, chemotherapy and immunotherapy in our hospital;
- Patients diagnosed in our hospital from January 2025 to December 2028;
- Have relatively complete clinical data;
- Age between 15 and 75 years old;
You may not qualify if:
- The final diagnosis of the participants is other diseases, including lymphoma, or oropharyngeal cancer, etc.;
- The participants failed to obtain pathological and imaging data for various reasons;
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 17, 2025
First Posted
September 30, 2025
Study Start
October 1, 2025
Primary Completion (Estimated)
December 1, 2028
Study Completion (Estimated)
December 1, 2028
Last Updated
September 30, 2025
Record last verified: 2025-09