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A Multi-Center Prospective Non-Interventional Observational Study on the Outcomes and Side Effects of Radical Multidisciplinary Treatment for Locally Advanced Head and Neck Malignancies

A Multi-Center Prospective Non-Interventional Observational Study on the Outcomes and Side Effects of Radical Multidisciplinary Treatment for Locally Advanced Head and Neck Malignancies

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000039813
Enrollment
Unknown
Registered
2020-11-10
Start date
2020-11-30
Completion date
Unknown
Last updated
2021-02-16

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

Conditions

Head and neck malignances

Interventions

group according to different treatment schemes:Nil

Sponsors

The First Medical Center of Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients are grouped by anatomic site and pathological types of the primary tumor(eg.Squamous cell carcinoma of the nasal cavity and sinuses, olfactory neuroblastoma, squamous cell carcinoma of the nasopharynx,oropharynx,hypopharynx and glottic larynx and so on); 2. Definitive pathological diagnosis locally advanced head and neck cancer; 3. KPS >= 70 or ECOC 0-1; 4. Patients are 18 to 70 years old; 5. Patients are supposed to survive over 2 years at least; 6. Imaging(MRI or enhanced MRI,or US)as a aid to identify the invision of surrounding tissue and lymph node metastesis; 7. The cervical and supraclavicular regional lymph node metastasis are allowed; 8. Patients are required to have normal hepatic, renal, and bone marrow function, without severe hematologic toxicity and severe complications. Surgery, induction chemotherapy, concurrent chemoradiotherapy, consolidation chemotherapy, targeted therapy and immunotherapy were allowed in the study; 9. Patients voluntarily participate in the study and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients have underwent palliative or incomplete tumor resection. 2. Patients who have poor hepatic and renal function, severe hematologic toxicity and complications can not tolerate surgery, induction chemotherapy, concurrent chemotherapy, consolidation chemotherapy, target therapy and immunotherapy and so on. 3. The area planed to be received radiotherapy had a history of irradiation. 4. Pregnant females.

Design outcomes

Primary

MeasureTime frame
acute side effects;late side effects;curative effect;

Countries

China

Contacts

Public ContactLin Ma

Department of Radiation Oncology, the First Medical Center of Chinese PLA General Hospital

malinpharm@sina.com+86 13911197589

Outcome results

None listed

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