Reduction of Postoperative Radiotherapy in Head and Neck Squamous Cell Carcinoma

Recruiting N/A Interventional Study
Head and Neck Squamous Cell Carcinoma (HNSCC)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 70
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
50 (estimated)
Sponsor
Sun Yat-sen University · Other
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About This Trial

To explore the control rate and quality of life of participants with late head and neck squamous cell carcinoma who have obtained postoperative pCR after cervical lymph node surgery with neoadjuvant chemotherapy combined with immunotherapy, and the cervical lymph node removal prophylactic irradiation ENI in the low-risk area.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Preoperative pathologically confirmed initial treatment of head and neck squamous cell carcinoma * Receive neoadjuvant chemotherapy combined with PD-1 monoclonal antibody immunotherapy, and meet one of the following conditions: Preoperative clinical stage was T3-T4 or N2-N3 (A…
Contacts

Chun-Yan Chen

020-87342926

chenchuny@sysucc.org.cn

CONTACT

Ya-Ni Zhang

020-87342926

zhangyn1@sysucc.org.cn

CONTACT