Patients with gastrointestinal, hepatobilial, urological, or otorhinolaryngological cancer treated with an immune chekpoint inhibitor
Conditions
Interventions
None listed
Sponsors
Osaka General Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: patients whom written informed consents of the study are obtained from
Exclusion criteria
Exclusion criteria: patients with past history of an immune checkpoint inhibitor
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| overall survival | — |
Secondary
| Measure | Time frame |
|---|---|
| progression-free survival objective response rate adverse events during the treatment | — |
Countries
Japan
Contacts
Public ContactYoshimichi Haruna
Osaka General Medical Center Department of Laboratory Medicine
Outcome results
None listed