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Case report: A persistently expanded T cell response in an exceptional responder to radiation and atezolizumab for metastatic non-small cell lung cancer

Most patients with advanced non-small cell lung cancer (NSCLC) do not achieve a durable remission after treatment with immune checkpoint inhibitors. Here we report the clinical history of an exceptional responder to radiation and anti-program death-ligand 1 (PD-L1) monoclonal antibody, atezolizumab,...

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Detalles Bibliográficos
Autores principales: Coffey, David G., Xu, Yuexin, Towlerton, Andrea M. H., Kowanetz, Marcin, Hegde, Priti, Darwish, Martine, Yadav, Mahesh, Blanchette, Craig, Ruppert, Shannon M., Bertino, Sarah, Xu, Qikai, Ferretti, Andrew, Weinheimer, Adam, Hellmann, Matthew, Qin, Angel, Thomas, Dafydd, Warren, Edus H., Ramnath, Nithya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500393/
https://www.ncbi.nlm.nih.gov/pubmed/36159875
http://dx.doi.org/10.3389/fimmu.2022.961105
Descripción
Sumario:Most patients with advanced non-small cell lung cancer (NSCLC) do not achieve a durable remission after treatment with immune checkpoint inhibitors. Here we report the clinical history of an exceptional responder to radiation and anti-program death-ligand 1 (PD-L1) monoclonal antibody, atezolizumab, for metastatic NSCLC who remains in a complete remission more than 8 years after treatment. Sequencing of the patient’s T cell repertoire from a metastatic lesion and the blood before and after anti-PD-L1 treatment revealed oligoclonal T cell expansion. Characterization of the dominant T cell clone, which comprised 10% of all clones and increased 10-fold in the blood post-treatment, revealed an activated CD8(+) phenotype and reactivity against 4 HLA-A2 restricted neopeptides but not viral or wild-type human peptides, suggesting tumor reactivity. We hypothesize that the patient’s exceptional response to anti-PD-L1 therapy may have been achieved by increased tumor immunogenicity promoted by pre-treatment radiation therapy as well as long-term persistence of oligoclonal expanded circulating T cells.