Evidence map›Paper›PMID 41275271›Full record

ArticleCancer imaging : the official publication of the International Cancer Imaging Society2025

Survival impact of a KEAP1-NFE2L2 radiomics model in PDL1 ≥ 50% non-small cell lung cancer treated with pembrolizumab: the PEMBROMIC study.

Coline Le Meur, Karim Amrane, Renaud Descourt, Matthieu Chasseray, Olivier Pradier, David Bourhis, Ronan Abgral, Vincent Bourbonne

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Article in Cancer imaging : the official publication of the International Cancer Imaging Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Coline Le MeurDepartment of Radiotherapy, University Hospital of Brest, Brest, France.
Karim AmraneDepartment of Oncology, Regional Hospital of Morlaix, Morlaix, France.
Renaud DescourtDepartment of Oncology, University Hospital of Brest, Brest, France.
Matthieu ChasserayDepartment of Radiotherapy, Pasteur Clinic, Brest, France.
Olivier PradierDepartment of Radiotherapy, University Hospital of Brest, Brest, France.
David BourhisDepartment of Nuclear Medicine, University Hospital of Brest, Brest, France.
Ronan AbgralDepartment of Nuclear Medicine, University Hospital of Brest, Brest, France.
Vincent BourbonneDepartment of Radiotherapy, University Hospital of Brest, Brest, France. vincent.bourbonne@chu-brest.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNew factors predicting response in patients with a PD-L1 tumor proportion score (TPS) ≥ 50% for locally advanced or metastatic non-small cell lung cancer (NSCLC) are needed to better select first-line therapy. Based on the literature, we previously developed a radiomic model predicting the KEAP1/NFE2L2 mutational status.

methodThis was a retrospective monocenter study including 94 consecutive patients with advanced or metastatic PD-L1 ≥ 50% NSCLC, treated with pembrolizumab, who underwent a pre-therapeutic FDG-PET/CT and were followed up for 1 year. Seventy-seven patients who did not progress within the first 60 days of treatment were analyzed. Each primary lesion was segmented by 2 physicians on PET and CT scans. Radiomic features were calculated using MIM software on both PET and CT imaging. A previously developed KEAP1/NFE2L2 radiomic prediction model (called MUT

resultsThe main characteristics of this cohort were: median age of 67.0 years [range, 48.0-84.0], sex ratio M/F = 60/17, 74.0% of patients with a histopathology of adenocarcinoma and 85.0% with a stage IV disease. The median follow-up was 20.0 months [range, 15.3-23.9]. Fifty-six (72.2%) patients experienced a disease progression with a median PFS of 11.8 months (CI95% 8.6-15.8) among which 51 (66.2%) died. In univariable analysis, MUT

conclusionIn PD-L1 TPS ≥ 50% NSCLC patients treated with pembrolizumab, our results suggest an improved PFS in patients predicted to be KEAP1/NFE2L2 mutated.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungKelch-Like ECH-Associated Protein 1Lung NeoplasmsNF-E2-Related Factor 2AgedAged, 80 and overB7-H1 AntigenFemaleHumansMaleMiddle AgedMutationPositron Emission Tomography Computed TomographyRadiomicsAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 AntigenCD274 protein, humanKEAP1 protein, humanKelch-Like ECH-Associated Protein 1NF-E2-Related Factor 2pembrolizumabFDG-PETImmune checkpoint inhibitorsKEAP1/NFE2L2Non-small cell lung cancerPembrolizumabRadiomic analysis

Identifiers

PMID41275271
PMCPMC12752150

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