Evidence map›Paper›PMID 41854264›Full record

Trial reportActa oncologica (Stockholm, Sweden)2026

How does pulmonary function impact QoL in patients with locally advanced NSCLC treated with chemoradiotherapy and durvalumab?

Frigg Å Sommervoll, Henrik Horndalsveen, Dag Einar Sommervoll, Jussi Koivonen, Tarje Onsøien Halvorsen, Bjørn Henning Grønberg, Marianne Aanerud, Saulius Cicenas, Nina Helbekkmo, Jarkko Ahvonen and 8 more

Registry-linked trialAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Acta oncologica (Stockholm, Sweden), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04392505 (Durvalumab), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04392505 phase2active not recruitingnot on this map

Durvalumab (MEDI4736) After chemoRadioTherapy (DART) for NSCLC Patients - a Phase II Translational and Biomarker Study Investigating PDL1 Positive and Negative Patients

TypeinterventionalSponsorOslo University HospitalRan2020 to 2033Enrolled100ConditionsCancer, Non Small Cell Lung Cancer, Non Small Cell Lung Cancer Stage III, NSCLCArmsDurvalumab Injection
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Frigg Å SommervollDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Henrik HorndalsveenDepartment of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway; Department of Oncology, Oslo University Hospital, Oslo, Norway; Department of Clinical Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0002-6806-6116
Dag Einar SommervollNMBU.
Jussi KoivonenDepartment of Oncology and Radiotherapy, Oulu University Hospital, Oulu, Finland; Medical Research Center Oulu, Oulu, Finland.ORCID 0000-0001-6425-1640
Tarje Onsøien HalvorsenDepartment of Clinical and Molecular Medicine, NTNU, Norwegian University of Science and Technology, Trondheim, Norway; Department of Oncology, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.ORCID 0000-0002-1181-921X
Bjørn Henning GrønbergDepartment of Clinical and Molecular Medicine, NTNU, Norwegian University of Science and Technology, Trondheim, Norway; Department of Oncology, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.ORCID 0000-0001-5744-1534
Marianne AanerudDepartment of Clinical Science, University of Bergen, Bergen, Norway; Department of Thoracic Medicine, Haukeland University Hospital, Bergen, Norway.
Saulius CicenasDepartment of Thoracic Surgery and Oncology, National Cancer Center, Affiliate of Vilnius University Hospital Santaros Klinikos, Lithuania.
Nina HelbekkmoDepartment of Pulmonology, University Hospital of North Norway, Tromsø, Norway.
Jarkko AhvonenTays Cancer Center, Department of Oncology, Tampere University Hospital, Tampere, Finland.ORCID 0000-0003-4335-5242
Maria SilvoniemiDepartment of Pulmonary Medicine, Turku University Hospital, Turku, Finland.ORCID 0000-0001-9203-7465
Gina BarreraDepartment of Pulmonology, Stavanger University Hospital, Stavanger, Norway.
Maria M BjaanæsDepartment of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway; Department of Oncology, Oslo University Hospital, Oslo, Norway.ORCID 0000-0003-0864-3628
Vilde Haakensen
Åsa ÖjlertDepartment of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway; Department of Oncology, Oslo University Hospital, Oslo, Norway.
Kersti OselinOncology and Haematology Clinic, North Estonia Medical Centre, Tallinn, Estonia.ORCID 0000-0002-3862-3882
Åslaug HellandDepartment of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway; Department of Oncology, Oslo University Hospital, Oslo, Norway; Department of Clinical Medicine, University of Oslo, Oslo, Norway. aslaug.helland@medisin.uio.no.ORCID 0000-0002-5520-0275
Tesfaye MadeboDepartment of Clinical Science, University of Bergen, Bergen, Norway; Department of Pulmonology, Stavanger University Hospital, Stavanger, Norway.ORCID 0000-0003-3043-5059

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImpaired pulmonary function is common among patients with lung cancer and may negatively affect health-related quality of life (HRQoL). The primary objective of the present sub-study of the DART-trial was to assess the overall quality of life changes during treatment and stratified by the presence of Chronic Obstructive Pulmonary Disease (COPD).

methodsThe investigator-initiated DART trial (NCT04392505) included patients with unresectable stage III non-small cell lung cancer (NSCLC) treated with chemoradiotherapy followed by durvalumab. Baseline pulmonary function was measured by spirometry, and patients were stratified by FEV1/FVC <70% (COPD) or ≥70% (non-COPD). HRQoL was assessed regularly using the EORTC QLQ-C30 and QLQ-LC13 questionnaires at screening and during treatment. A difference in mean score of ≥10 was defined as clinically significant.

resultsA total of 86 patients initiated durvalumab and completed at least one HRQoL assessment; pulmonary function data were available for 64 patients. For the overall cohort, quality of life scores remained stable throughout treatment. Patients with COPD consistently reported lower global health scores than those with preserved lung function. The global health score among patients with COPD was not significantly different at end of treatment compared to baseline, however significantly lower than patients without COPD. Symptom trajectories across QLQ-C30 scales were stable in both groups. Dyspnoea was more prevalent among patients with COPD. In the LC13 module, no clinically significant differences were observed except for dyspnoea, which was consistently higher among patients with COPD.

interpretationThe HRQoL remained stable during chemoradiotherapy and durvalumab treatment in stage III NSCLC patients. Impaired lung function was associated with modestly lower HRQoL, though larger studies are needed to confirm subgroup effects.

Indexed as

Antibodies, MonoclonalCarcinoma, Non-Small-Cell LungChemoradiotherapyLungLung NeoplasmsPulmonary Disease, Chronic ObstructiveQuality of LifeAgedAntineoplastic Agents, ImmunologicalFemaleHumansMaleMiddle AgedNeoplasm StagingRespiratory Function TestsAntibodies, MonoclonalAntineoplastic Agents, Immunologicaldurvalumab

Identifiers

PMID41854264
PMCPMC13006962

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.