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dc.contributor.authorHorndalsveen, Henrik
dc.contributor.authorAlver, Tine Norman
dc.contributor.authorDalsgaard, Astrid Marie
dc.contributor.authorHelbekkmo, Nina
dc.contributor.authorGrønberg, Bjørn Henning
dc.contributor.authorHalvorsen, Tarje Onsøien
dc.contributor.authorRamberg, Christina
dc.contributor.authorHaakensen, Vilde Drageset
dc.contributor.authorØjlert, Åsa Kristina
dc.contributor.authorBjaanæs, Maria Moksnes
dc.contributor.authorHelland, Åslaug
dc.contributor.authorRogg, Lotte Victoria
dc.date.accessioned2023-02-27T10:04:03Z
dc.date.available2023-02-27T10:04:03Z
dc.date.issued2022-11-04
dc.description.abstractThe introduction of immune checkpoint inhibitors has transformed the treatment landscape of metastatic non-small cell lung cancer. However, challenges remain to increase the fraction of patients achieving durable clinical responses to these drugs and to help monitor the treatment effect. In this phase II trial, we investigated the toxicity, systemic responses and circulating tumour DNA responses in patients (n = 21) with advanced non-small-cell lung cancer treated with atezolizumab and stereotactic body radiotherapy in the second or later line. We found the combined treatment to be safe with grade 3 toxicity reported in three patients. As the best overall response, four patients had a partial response, eight had stable disease and five had progressive disease. Median overall survival time was still not reached after a median follow-up of 26.5 months and 10/15 patients with programmed death-ligand 1 negative tumours were alive >18 months after the start of the study treatment. ctDNA was detectable at baseline in 11 patients. A rapid decline in ctDNA to <30% of baseline levels was seen in three patients, two of which were radiographic responders and one was considered clinically benefiting from therapy for almost 1 year.en_US
dc.identifier.citationHorndalsveen H, Alver TN, Dalsgaard, ROGG LV, Helbekkmo NH, Grønberg BH, Halvorsen T, Ramberg C, Haakensen V, Øjlert ÅK, Bjaanæs MM, Helland Å. Atezolizumab and stereotactic body radiotherapy in patients with advanced non-small cell lung cancer: safety, clinical activity and ctDNA responses—the ComIT-1 trial. Molecular Oncology. 2022en_US
dc.identifier.cristinIDFRIDAID 2070231
dc.identifier.doi10.1002/1878-0261.13330
dc.identifier.issn1574-7891
dc.identifier.issn1878-0261
dc.identifier.urihttps://hdl.handle.net/10037/28612
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.journalMolecular Oncology
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleAtezolizumab and stereotactic body radiotherapy in patients with advanced non-small cell lung cancer: safety, clinical activity and ctDNA responses—the ComIT-1 trialen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution 4.0 International (CC BY 4.0)