Quality of life during adjuvant immunotherapy for locally advanced non-small cell lung cancer
Official title: Self-reported Health During Adjuvant Immunotherapy for Locally Advanced Lung Cancer - the ImmLungCare Project.
Run by Göteborg University · NCT07754409 · Data updated 2026-11-12
This study looks at how patients feel and cope during a year of immunotherapy after chemoradiotherapy for locally advanced non-small cell lung cancer.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 75 (estimated) |
| Sponsor | Göteborg University Academic / other |
| Drugs / interventions | immunotherapy |
| Locations | 1 site (Gothenburg) |
| Status | Recruiting |
| Started | September 1, 2026 |
| Main results expected | December 31, 2028 |
| Study ends | December 31, 2029 |
| Registry record updated | September 2, 2026 |
| Trial ID | NCT07754409 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) with locally advanced NSCLC treated at the participating centers and planned for 12 months of concurrent chemoradiotherapy plus immune checkpoint inhibitor therapy, with adequate Swedish language understanding.
✕Probably not a fit
Patients with significant comorbidities or language barriers that preclude informed consent may not experience or report the intended quality-of-life outcomes.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study follows adults with locally advanced NSCLC who are receiving concurrent chemoradiotherapy plus a year of immune checkpoint inhibitors. It aims to document self-reported health and quality of life during treatment, recognizing that immunotherapy can cause unique and late-appearing side effects. Data are collected at two specialized oncology centers in Sweden to understand how patients endure this additional therapy and what factors influence well-being. The results may guide supportive care and inform future patient management during adjuvant immunotherapy. No experimental interventions are being tested in this design; the focus is on observation of real-world experiences and outcomes.
Why it matters
Potential benefit: If successful, the study could identify patterns in quality of life and distress that inform better supportive care and patient counseling during adjuvant immunotherapy.
How similar studies have gone: Previous work in oncology has shown that patient-reported outcomes during immunotherapy are feasible to collect, though data in the adjuvant, locally advanced setting are limited and ongoing.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with locally advanced non-small lung cancer * cared for at either one of two specialized oncology centres * ≥ 18 years of age * planned for concurrent chemoradiotherapy including ICI for 12 months * performance status 0-2. Exclusion Criteria: * diseases or comorbidities that may have significant impact on the outcome variables * limited understanding of the Swedish language preventing the possibility to give oral and written informed consent.
Where it's running
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Department of Oncology, Sahlgrenska University Hospital
Gothenburg, Sweden Recruiting
Study contacts
- Study coordinator: Sofie Jakobsson, Associated professor
- Email: sofie.jakobsson@fhs.gu.se
- Phone: +46766182858
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.