International Collaborative Study on AJCC/UICC TNM-10 for Nasopharyngeal Cancer

NCT07013461 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 5000

Last updated 2026-05-04

No results posted yet for this study

Summary

The goal of this international, multicenter, prospective observational study is to improve prognostication and prediction of failure pattern for nasopharyngeal carcinoma (NPC), in order to provide more accurate guidance for personalized treatment decision. Firstly, we aim to improve the fundamental TNM staging system \[The American Joint Committee on Cancer(AJCC)/Union for International Cancer Control(UICC) TNM Version-Nine\] based on universally assessable anatomical parameters. Secondly, we aim to further refine prognostication for individual patients by integrating anatomical TNM parameters with non-anatomical factors and molecular biomarkers. In addition to the core group of participating centers from China (including Hong Kong) where NPC is most prevalent, the study will enrol patients from multiple countries/regions including those from non-endemic areas to provide global data. Patients treated with contemplary treatment methods during October 2025 to September 2026 will be recruited and they will be followed up for 5 years to generate detailed records for robust evaluation.

Key Questions:

* To achieve optimal improvement of anatomically based AJCC/UICC TNM Classification for global application
* To achieve precise prediction of failure pattern for individual patients by integration of TNM system and non-anatomical prognostic factors/molecular biomarkers Recruited patients with confirmed histological diagnosis of NPC will undergo standard clinical evaluations and receive treatment per institutional guidelines.

The anatomical extent of disease at presentation will be evaluated by experienced radiologists and oncologists. The patient will be followed up for 5 years and clinical outcome will be recorded for analyses on correlation with prognostic factors.

This study will be another important milestone for NPC staging because firstly, this is the first time that the data are based on prospective data to ensure comprehensive coverage of all essential evidence; and secondly, this is the first time that centers from non-endemic countries/regions will also participate to ensure that the final recommendations are globally applicable. The findings will provide valuable evidence for the development of the AJCC/UICC TNM Version-Ten staging system and prognostic system to improve risk stratification for designing personalized treatment strategy, ultimately leading to improvement of patient outcome and patient selection for future research worldwide.

Conditions

  • Nasopharyngeal Cancinoma (NPC)

Sponsors & Collaborators

  • Fujian Cancer Hospital

    collaborator OTHER_GOV
  • Chinese Academy of Medical Sciences

    collaborator OTHER
  • Jiangxi Provincial Cancer Hospital

    collaborator OTHER
  • Zhejiang Cancer Hospital

    collaborator OTHER
  • Chongqing University Cancer Hospital

    collaborator OTHER
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • Sichuan Cancer Hospital and Research Institute

    collaborator OTHER
  • First Affiliated Hospital of Fujian Medical University

    collaborator OTHER
  • Queen Mary Hospital, Hong Kong

    collaborator OTHER
  • The Queen Elizabeth Hospital

    collaborator OTHER
  • Pamela Youde Nethersole Eastern Hospital

    collaborator OTHER
  • Princess Margaret Hospital, Hong Kong

    collaborator OTHER_GOV
  • United Christian Hospital

    collaborator OTHER
  • Prince of Wales Hospital, Shatin, Hong Kong

    collaborator OTHER
  • Fudan University

    collaborator OTHER
  • Hunan Cancer Hospital

    collaborator OTHER
  • National Cancer Center Singapore, Singapore

    collaborator UNKNOWN
  • Sun Yat-Sen University Cancer Center

    collaborator OTHER
  • Tuen Mun Hospital

    collaborator OTHER_GOV
  • The University of Hong Kong-Shenzhen Hospital

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-01-09
Primary Completion
2031-12-31
Completion
2031-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07013461 on ClinicalTrials.gov