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dc.contributor.authorAhlborn, LBen
dc.contributor.authorTuxen, IVen
dc.contributor.authorMouliere, Florenten
dc.contributor.authorKinalis, Sen
dc.contributor.authorSchmidt, AYen
dc.contributor.authorRohrberg, KSen
dc.contributor.authorSantoni-Rugiu, Een
dc.contributor.authorNielsen, FCen
dc.contributor.authorLassen, Uen
dc.contributor.authorYde, CWen
dc.contributor.authorOestrup, Oen
dc.contributor.authorMau-Sorensen, Men
dc.description.abstractPurpose: We evaluated longitudinal tracking of BRAF V600E in circulating cellfree DNA (cfDNA) as a marker of treatment response to BRAF inhibitor (BRAFi) combination therapies in non-melanoma solid tumors included in the Copenhagen Prospective Personalized Oncology (CoPPO) program. Experimental design: Patients with BRAF V600E-mutated tumors were treated with combination therapies including BRAFi. Quantification of mutant cfDNA from plasma was determined and correlated to clinical outcomes. Exome sequencing was performed to identify possible resistance mutations. Results: Twenty-three patients had BRAF-mutated tumors out of 455 patients included in CoPPO and 17 started BRAFi combination (EGFRi/MEKi) therapy. Tumor responses were achieved in 8 out of 16 evaluable patients and the median overalland progression-free survival (OS and PFS) was 15 and 4.8 months, respectively. Longitudinal measurements of BRAF V600E-mutant cfDNA indicated disease progression prior to radiological evaluation and a reduction in the mutant fraction of more than 50% after 4 and 12 weeks of therapy was associated with a significantly longer PFS (p=0.003 and p=0.029) and OS (p=0.029 and p=0.017). Furthermore, the baseline mutant fraction and total level of cfDNA positively correlated with tumor burden (p=0.026 and p=0.024). Finally, analysis of cfDNA at progression revealed novel mutations potentially affecting the MAPK pathway. Conclusion: BRAFi combination therapies showed a response rate of 50% in BRAF V600E-mutated non-melanoma tumors. The fraction of BRAF-mutant cfDNA represent a sensitive indicator for clinical outcomes with plasma collected at week 4 and 12 as crucial time points for monitoring response and disease progression.
dc.description.sponsorshipThis study was supported by the Danish Cancer Society, The Harboe Foundation, and the Oncological Research Fund, Department of Oncology, Copenhagen University Hospital, Denmark.
dc.rightsAttribution 4.0 International
dc.titleCirculating tumor DNA as a marker of treatment response in BRAF V600E mutated non-melanoma solid tumorsen
dc.contributor.orcidMouliere, Florent [0000-0001-7043-0514]
rioxxterms.typeJournal Article/Reviewen

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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International