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A two-center single-arm clinical study of radiotherapy combined with anrotinib in the treatment of locally advanced unresectable adenoid cystic carcinoma of the head and neck

A two-center single-arm clinical study of radiotherapy combined with anrotinib in the treatment of locally advanced unresectable adenoid cystic carcinoma of the head and neck

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111505
Enrollment
Unknown
Registered
2025-10-31
Start date
2021-06-20
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

adenoid cystic carcinoma of the head and neck

Interventions

Intervention group:Radiotherapy combined with anlotinib

Sponsors

Eye, Ear, Nose & Throat Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged > 18 years old and 2000/mm^3, platelet count > 100,000/mm^3 9. Liver and renal function examinations before treatment meet the following criteria: bilirubin 60 ml/min 10. Signed informed consent form before the start of the study

Exclusion criteria

Exclusion criteria: 1. Head and neck malignant tumors with a pathological type other than adenoid cystic carcinoma 2. Cases not jointly discussed with head and neck surgeons 3. Early-stage head and neck adenoid cystic carcinoma (ACC) or head and neck ACC that can be completely resected by surgery 4. Evidence or suspicious evidence of distant metastasis found in clinical examination or imaging examination 5. Not receiving treatment for the first time (i.e., prior anti-tumor treatment history) 6. History of malignant tumors or concurrent multiple primary tumors (except basal cell carcinoma of the skin) 7. Positive pregnancy test result in women of childbearing age 8. Concurrent diseases or conditions that affect the patient’s normal enrollment or safety during the study 9. Active mental disorders or other psychological illnesses that affect the patient’s ability to sign the informed consent form and understand the study 10. Uncontrolled active infection

Design outcomes

Primary

MeasureTime frame
Local Control Rate;Distant Disease-Free Survival rate;Overall survival rate;

Secondary

MeasureTime frame
Eyeball retention rate;

Countries

China

Contacts

Public ContactShengzi Wang, Xiaoshen Wang, Li Wang

Eye, Ear, Nose & Throat Hospital of Fudan

xiaoshen.wang@fdeent.org+86 21 3423 3877

Outcome results

None listed

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