About this trial
The study is designed as a prospective, single-arm observational, mixed-method study. Patients with stage IV NSCLC or inoperable mesothelioma will be included and will be treated with immunotherapy according to current guidelines and standard of care. Patients may receive either a PD1/L1 inhibitor monotherapy or, if indicated, together with a CTLA4 inhibitor. Immunotherapy may be administered alone or together with chemotherapy as per site standard/physician's choice. Patients will be given access to a mobile app. Patients will receive daily questions via the app to assess immune-related adverse events between clinic visits and their well-being.
Eligibility criteria
Qualifiers
Signed Informed Consent Form
Age > 18 years at the time of study entry
Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2
Life expectancy > 6 months
Disqualifiers
Previous systemic treatment for metastatic or locally advanced disease
Trial design
Treatments tested in this trial
- Not listed