influenza
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1 Lung cancer patients aged 50 years or older receiving immune checkpoint inhibitors And 2 Who receive influenza vaccine at their own will and have voluntarily agreed to participate in this study
Exclusion criteria
Exclusion criteria: 1 Patients who have been vaccinated with influenza vaccine in the 2020/2021 season 2 Patients who have had anaphylaxis due to the components of influenza vaccine, or those who may have allergies 3 Patients with egg allergies 4 Influenza infected patients in 2020/2021 season 5 Patients who suffered from acute febrile illness or other serious illness at the timing of vaccination 6 Those who received a cytotoxic agent within 1 month of vaccination 7 Those who are taking steroids / immunosuppressants (excluding administration as antiemetics) 8 Others who are not suitable for vaccination
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| seroprotection rate 3 to 5 weeks after the vaccination | — |
Secondary
| Measure | Time frame |
|---|---|
| geometric mean titer before and 3 to 5 weeks after the vaccination mean fold rises, seroresponse rate, seroconversion rate 3 to 5 weeks after the vaccination presence of immune-related adverse events within 6 months of the vaccination | — |
Countries
Japan
Contacts
Kameda Medical Center Department of Pulmonology