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

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age15-75
SponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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;

Disqualifiers

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.

Trial population

Patients with nasopharyngeal carcinoma who were admitted to our hospital

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • No Intervention

    Other intervention

    This project involves no therapeutic intervention for the subjects.

Treatment groups

600 Participants
are divided into 1 treatment group
Group A: Study Groups1 intervention

Trial outcomes

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

Time frame
3-year

Secondary outcomes

1

Overall survival (OS)

Overall survival is measured from day of diagnosis until death due to any cause or the latest known date alive

Time frame
5-year

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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