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A Bidirectional Study of Individualized Postoperative Adjuvant Treatment Decision Model for Locally Advanced Head and Neck Squamous Cell Carcinoma Based on Multimodal Dynamic Data

A Bidirectional Study of Individualized Postoperative Adjuvant Treatment Decision Model for Locally Advanced Head and Neck Squamous Cell Carcinoma Based on Multimodal Dynamic Data

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500107027
Enrollment
Unknown
Registered
2025-08-01
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Locally Advanced Head and Neck Squamous Cell Carcinoma

Interventions

Postoperative concurrent chemoradiotherapy group:N/A
Postoperative radiotherapy group:N/A
Postoperative observation group:N/A

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Retrospective Study: 1)Age >= 18 years; 2)Patients diagnosed and treated at Nanfang Hospital, Southern Medical University between January 2017 and June 2022, with no further clinical visits after June 2024 and lost to follow-up; 3)Newly diagnosed head and neck squamous cell carcinoma (HNSCC) confirmed by histopathology; 4)Locally advanced disease without distant metastasis; 5)Complete clinical data (including patient demographics, tumor characteristics, treatment details, and prognostic variables); 6)Availability of MRI, CT, or PET-CT images before and after radical treatment. 2.Prospective Study: 1) Voluntary provision of signed informed consent; 2) Age >= 18 years; 3) Newly diagnosed head and neck squamous cell carcinoma (HNSCC) confirmed by histopathology; 4) Locally advanced disease without distant metastasis; 5) Complete clinical data (including patient demographics, tumor characteristics, treatment details, and prognostic variables); 6) Availability of MRI, CT, or PET-CT images before and after radical treatment.

Exclusion criteria

Exclusion criteria: 1.History of or coexisting secondary malignancies. 2.Lack of definitive radical treatment. 3.Absence of baseline or follow-up imaging (MRI/CT/PET-CT). 4.Investigator-determined unsuitability for study participation.

Design outcomes

Primary

MeasureTime frame
3-year regional relapse-free survival;

Secondary

MeasureTime frame
3-year Progression free survival;3-year overall survival;

Countries

China

Contacts

Public ContactBei Chen

Southern Medical University Southern Hospital

bzcheese@126.com+86 158 8993 2906

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026