Clinical Trials Logo

Clinical Trial Summary

The response rate of HNSCC to immune checkpoint blockade was not satisfied. Improving the mPR rate of neoadjuvant immunotherapy through the combination with other treatment methods is an important way to further improve the prognosis of such patients. This study aims to explore the efficacy and safety of PD-1 monoclonal antibody with neoadjvant SBRT and chemotherapy. The triple mode not only can Increase the effectiveness of neoadjuvant therapy,meanwhile,the in situ tumor vaccine inoculation effect generated by enhancing the release of specific antigens after tumor radiotherapy with PD-1 monoclonal antibody achieves a sustained anti-tumor immune effect throughout the body, reducing postoperative adjuvant radiotherapy and chemotherapy. The triple mode has important exploratory value in achieving high quality and long-term survival for patients, and may provides a more efficient mode for locally advanced HNSCC.


Clinical Trial Description

locally advanced HNSCC patients would receive PD-1 antibody and chemotherapy with or without SBRT covering GTV of primary disease and metastatic nodes , followed by surgery. pathological response was measured .Neoadjuvant PD-1 antibody and chemotherapy with certuxmab was also tested ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06306846
Study type Interventional
Source Zhejiang Cancer Hospital
Contact Feng Jiang, MD
Phone 0086-571-88128202
Email jiangfeng@zjcc.org.cn
Status Recruiting
Phase Phase 2
Start date October 1, 2023
Completion date December 31, 2026

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05039606 - Clinical Study of Radiotherapy Combined With Nedaplatin Contrast and Cisplatin for the Treatment of Locally Advanced Head and Neck Squamous Carcinoma Phase 2
Completed NCT04361409 - Rituximab Plus Chemotherapy in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma Phase 1
Recruiting NCT00634595 - Trial of E10A in Head and Neck Cancer Phase 2
Recruiting NCT05552807 - SCT200 in Combination With SCT-I10A/Paclitaxel/Docetaxel in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma Phase 1