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Efficacy and safety analysis of PD-1 inhibitor advanced head and neck squamous cell carcinoma

Efficacy and safety analysis of PD-1 inhibitor advanced head and neck squamous cell carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091124
Enrollment
Unknown
Registered
2024-10-21
Start date
2021-04-05
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

Head and neck squamous cell carcinoma

Interventions

Group of patients with head and neck squamous cell carcinoma:None

Sponsors

Oral and Maxillofacial Surgery, Cangzhou central hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Pathological diagnosis (surgical pathological section or needle biopsy) for HNSCC; 2. The stage is stage IV (according to the 8th edition of the AJCC Cancer Staging Manual); 3. The clinical stage is stage I, II or III, local recurrence or distant metastasis after radical resection; 4. Presence of evaluable lesions on imaging; 5. ECOG score of 0-1 points; 6. Have not received chemoradiotherapy in the past, or have stopped treatment for at least 6 months; 7. Have complete clinical records and follow-up data

Exclusion criteria

Exclusion criteria: 1. Patients who have received immunotherapy such as CTLA-4 inhibitors and PD-1 inhibitors in the past; 2. ECOG > 2 points, expected survival time less than 3 months; 3. Recent systemic active infection or acute exacerbation of chronic diseases, unable to tolerate chemotherapy; 4. Previous autoimmune diseases and hematologic diseases; 5. Previous or concurrent malignant tumors or serious and uncontrollable diseases other than HNSCC.

Design outcomes

Primary

MeasureTime frame
Overall survival;Progression-free survival ;

Countries

China

Contacts

Public ContactQi Mengchun

Oral and Maxillofacial Surgery, Cangzhou central hospital

13931711222@163.com+86 139 3171 1222

Outcome results

None listed

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