Clinical trial Recruiting at 1 site Observational Ages 18 and up

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.

More Carcinoma, Non-Small-Cell Lung trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment75 (estimated)
SponsorGöteborg University
Academic / other
Drugs / interventionsimmunotherapy
Locations1 site (Gothenburg)
StatusRecruiting
StartedSeptember 1, 2026
Main results expectedDecember 31, 2028
Study endsDecember 31, 2029
Registry record updatedSeptember 2, 2026
Trial IDNCT07754409 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

  • Department of Oncology, Sahlgrenska University Hospital
    Gothenburg, Sweden
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.