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A Single-Center Retrospective Clinical Study on Adenoid Cystic Carcinoma of the Head and Neck

A Single-Center Retrospective Clinical Study on Adenoid Cystic Carcinoma of the Head and Neck

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119106
Enrollment
Unknown
Registered
2026-02-23
Start date
2026-02-23
Completion date
Unknown
Last updated
2026-03-02

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

Postoperative concurrent chemoradiotherapy group:None
Postoperative radiotherapy alone group:None
Surgery-only group:None
Postoperative chemotherapy only group:None

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 15-80 years (inclusive of 15 and 80 years); 2. Histologically diagnosed with adenoid cystic carcinoma of the head and neck, without distant metastasis; 3. Radiotherapy methods include static or dynamic intensity-modulated radiotherapy, with a planned cumulative radiation dose of >= 60 Gy; the concurrent chemotherapy drug is cisplatin; 4. No previous radiotherapy or chemotherapy for head and neck tumors; 5. ECOG score: 0-2; 6. Good function of major organs, that is, within 14 days before randomization, the relevant test indicators meet the following requirements: a. Blood routine examination: hemoglobin >= 80 g/L (no blood transfusion within 14 days); neutrophil count > 1.5×10^9/L; platelet count >= 80×10^9/L; b. Biochemical examination: total bilirubin = 60 ml/min (Cockcroft-Gault formula); 7. Cardiac Doppler ultrasound assessment: left ventricular ejection fraction (LVEF) >= 50%

Exclusion criteria

Exclusion criteria: 1.Previously received radiation therapy or chemotherapy for head and neck tumors; 2.Patients receiving neoadjuvant therapy before surgery; 3.Complicated with serious heart, lung, liver, kidney, digestive system, hematopoietic system and nervous system diseases, acute infectious diseases, autoimmune diseases, HIV, Poor blood sugar control; 4.Pregnant or lactating female; 5.Allergic constitution (such as those known to be allergic to two or more drugs); 6.Patients with severe mental illness, a history of alcohol or drug abuse;

Design outcomes

Primary

MeasureTime frame
Overall Survival;

Secondary

MeasureTime frame
Progression-free survival;

Countries

China

Contacts

Public ContactKunyu Yang

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

yangkunyu1@hotmail.com+86 27 8587 1855

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026