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The value of definitive chemoradiotherapy in the treatment of advanced sinonasal squamous cell carcinoma with orbital preservation

The value of definitive chemoradiotherapy in the treatment of advanced sinonasal squamous cell carcinoma with orbital preservation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036029
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-11-01
Completion date
Unknown
Last updated
2020-08-31

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

Conditions

sinonasal squamous cell carcinoma

Interventions

Group 2:definitive chemotherapy

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. Voluntary participation and written informed consent; 2. Aged 18-70 years old, male or female; 3. Pathological proved primary sinonasal squamous cell carcinoma; 4. Clinical stage III-IVb, without distant metastasis; 5. Measurable tumor volume; 6. Karnofsky score >=70, expected survival time >=6 months; 7. Blood routine test, liver, renal function and heart function are tolerant to chemoradiotherapy; 8. No history of mental illness; no drug addiction; 9. Gestational age should take effective contraceptive measures; Patients with good compliance are expected.

Exclusion criteria

Exclusion criteria: 1. Patients with other malignant tumors; 2. Patients with a history of head and neck malignancy, unless they have not received radiotherapy and the disease has not progressed for more than 2 years; 3. Patients who have participated in other clinical trials within one month before the trial; 4. Patients with serious neurological or mental diseases; 5. Pregnant, lactating patients, patients in the reproductive period without taking effective contraceptive measures; 6. Persons without personal freedom or independent capacity for civil conduct7Patients is not suitable to participate evaluated by the researcher.

Design outcomes

Primary

MeasureTime frame
overall survival;progression-free survival;

Countries

China

Contacts

Public ContactXinmao Song

Eye, Ear, Nose & Throat Hospital of Fudan University

muqinger@sina.com+86 18917785084

Outcome results

None listed

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