Skip to content

A Real-World Study Comparing the Efficacy of Nimotuzumab Combined with Concurrent Chemoradiotherapy and Concurrent Chemoradiotherapy Alone in Patients with High-Risk Locally Advanced Squamous Cell Carcinoma of the Head and Neck After Surgery

A Real-World Study Comparing the Efficacy of Nimotuzumab Combined with Concurrent Chemoradiotherapy and Concurrent Chemoradiotherapy Alone in Patients with High-Risk Locally Advanced Squamous Cell Carcinoma of the Head and Neck After Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111656
Enrollment
Unknown
Registered
2025-11-04
Start date
2025-11-10
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

High-Risk Locally Advanced Squamous Cell Carcinoma of the Head and Neck

Interventions

Concurrent Chemoradiotherapy:None
Nimotuzumab Combined with Concurrent Chemoradiotherapy:None

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Histopathological diagnosis of HNSCC. 2. Age between 20 and 70 years. 3. ECOG score of 0-1. 4. Adequate hematological, renal, and hepatic function. 5. All patients underwent radical surgical treatment. 6. All patients received adjuvant concurrent chemoradiotherapy or concurrent chemoradiotherapy combined with nimotuzumab. 7. AJCC (8th edition) locally advanced squamous cell carcinoma of the head and neck: III, IVA, and IVB. 8. All patients had one or more of the following high-risk factors, such as T3-4, N2-3, lymph nodes located in level IV or V, vascular invasion, perineural invasion, positive or close margins, and extracapsular spread of lymph nodes. 9. The clinical medical records of the patients were complete.

Exclusion criteria

Exclusion criteria: 1. Nasopharyngeal carcinoma. 2. Allergy to nimotuzumab or its components.

Design outcomes

Primary

MeasureTime frame
Overall survival;

Secondary

MeasureTime frame
Progression-free survival;Safety;

Countries

China

Contacts

Public ContactTong Gangling

Peking University Shenzhen Hospital

tgl221747@sohu.com+86 151 0755 9056

Outcome results

None listed

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