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. 2024 Oct 1;3:44. doi: 10.1186/s44215-024-00169-z

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 1 — Computed tomography (CT) and positron emission tomography (PET) before chemoradiotherapy (CRT) followed by durvalumab. a CT at the initial diagnosis revealed a tumor of 3.1 cm in diameter originating from the left upper lobe in the left superior sulcus that was in contact with the chest wall and enlarged hilar, periaortic, and left supraclavicular lymph nodes. b, c Fluorodeoxyglucose (FDG)-PET revealed uptake in the primary lesion, left supraclavicular lymph nodes, mediastinal lymph nodes, and periaortic lymph nodes. The maximum standardized uptake value on FDG-PET in the primary lesion was 14.1