Nasopharyngeal Carcinoma Clinical Trials

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International Collaborative Study to Develop the AJCC/UICC TNM Version-Ten for Nasopharyngeal Cancer

Status: Recruiting
Location: See location...
Study Type: Observational
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• All histologically confirmed nasopharyngeal carcinoma treated between 1 Oct 2025 and 30 Sep 2026

Locations
Other Locations
China
The University of Hong Kong-Shenzhen Hospital
RECRUITING
Shenzhen
Time Frame
Start Date: 2026-01-09
Estimated Completion Date: 2031-12-31
Participants
Target number of participants: 5000
Treatments
Patients with histologically confirmed NPC
All enrolled patients will receive diagnosis and treatment according to the standard clinical practice of each participating center.
Related Therapeutic Areas
Sponsors
Collaborators: Jiangxi Provincial Cancer Hospital, Hunan Cancer Hospital, Tuen Mun Hospital, Queen Mary Hospital, Hong Kong, Sun Yat-Sen University Cancer Center, Fudan University, The Queen Elizabeth Hospital, United Christian Hospital, Princess Margaret Hospital, Hong Kong, National Cancer Centre, Singapore, First Affiliated Hospital of Fujian Medical University, Prince of Wales Hospital, Shatin, Hong Kong, Sichuan Cancer Hospital and Research Institute, Chinese Academy of Medical Sciences, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Pamela Youde Nethersole Eastern Hospital, Zhejiang Cancer Hospital, Fujian Cancer Hospital, Chongqing University Cancer Hospital
Leads: The University of Hong Kong-Shenzhen Hospital

This content was sourced from clinicaltrials.gov