None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ? Patients with larynx, oral cavity, oropharynx, nasal cavity, maxillary sinus, hypopharyngeal carcinoma confirmed histologically as squamous cell carcinoma ? Patients who have undergone palliative chemotherapy for relapse after surgery or initial metastasis ? Patients who have received immune checkpoint inhibitors
Exclusion criteria
Exclusion criteria: ? Nasopharyngeal cancer patients ? Patients who have not been observed after a single dose of immune checkpoint inhibitors (follow-up loss) are difficult to confirm the effects or adverse events
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Objective response rate | — |
Secondary
| Measure | Time frame |
|---|---|
| Progression Free Survival;Duration of response;Overall Survival;Incidence of Hyperprogression;Incidence of Immune related adverse events | — |
Countries
Korea, Republic of
Contacts
Chung-Ang Univerisity Hospital