International Collaborative Study on AJCC/UICC TNM-10 for Nasopharyngeal Cancer
NCT ID: NCT07013461
Last Updated: 2025-06-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
5000 participants
OBSERVATIONAL
2025-10-01
2031-12-31
Brief Summary
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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.
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Detailed Description
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Recent years have witnessed transformative changes in NPC treatment paradigms, including advancements in radiotherapy techniques, the integration of immune checkpoint inhibitors, and intensified treatment for metastatic disease. In addition, studies have demonstrated the independent prognostic value of non-anatomical factors such as circulating EBV DNA levels, and various hematologic biomarkers. These developments necessitate continual improvement of the TNM staging system to align with contemporary management with diagnostic and therapeutic advancements.
This international, multicenter, prospective observational study is designed to address these critical requirements to generate high-quality evidence for developing the next generation TNM staging system (AJCC/UICC Version-Ten). The study will enroll all consecutive histopathological confirmed NPC patients treated during October 2025 and September 2026 from leading cancer centers worldwide. Detailed data on clinicopathological characteristics, imaging findings, molecular markers (including EBV-DNA), treatment and outcome will be collected and analyzed.
The primary endpoint of the study is overall survival (OS), while secondary endpoints focus on the pattern of failure at different sites: local failure-free survival (L-FFS), regional nodal failure-free survival (N-FFS), and distant failure-free survival (D-FFS). Correlation of these outcomes to anatomical and non-anatomical factors will be analyzed.
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
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients with histologically confirmed NPC
All enrolled patients will receive diagnosis and treatment according to the standard clinical practice of each participating center.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Sun Yat-sen University Cancer Hosptial
UNKNOWN
Fujian Cancer Hospital
OTHER_GOV
Chinese Academy of Medical Sciences
OTHER
Jiangxi Provincial Cancer Hospital
OTHER
Zhejiang Cancer Hospital
OTHER
Chongqing University Cancer Hospital
OTHER
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
OTHER
Sichuan Cancer Hospital and Research Institute
OTHER
First Affiliated Hospital of Fujian Medical University
OTHER
Queen Mary Hospital, Hong Kong
OTHER
The Queen Elizabeth Hospital
OTHER
Pamela Youde Nethersole Eastern Hospital
OTHER
Tuen Mun Hospital, Hospital Authority, Hong Koong
UNKNOWN
Princess Margaret Hospital, Hong Kong
OTHER_GOV
United Christian Hospital
OTHER
Prince of Wales Hospital, Shatin, Hong Kong
OTHER
Fudan University
OTHER
The University of Hong Kong-Shenzhen Hospital
OTHER
Responsible Party
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Anne Wing-mui Lee
Consultant, Clinical Cancer Center
Other Identifiers
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hkuszh2025075
Identifier Type: -
Identifier Source: org_study_id
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