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Prospective assessment using (18)F-FDG PET/CT as a novel predictor for early response to PD-1 blockade in non-small-cell lung cancer

Anti-programmed death-1 (PD-1) blockade is a standard treatment for advanced non-small-cell lung cancer (NSCLC). However, no appropriate modality exists for monitoring its therapeutic response immediately after initiation. Therefore, we aimed to elucidate the clinical relevance of (18)F-FDG PET/CT v...

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Autores principales: Yamaguchi, Ou, Kaira, Kyoichi, Naruse, Ichiro, Umeda, Yukihiro, Honda, Takeshi, Watanabe, Satoshi, Ichikawa, Kosuke, Tateishi, Kazunari, Kasahara, Norimitsu, Higuchi, Tetsuya, Hashimoto, Kosuke, Shinomiya, Shun, Miura, Yu, Shiono, Ayako, Mouri, Atsuto, Imai, Hisao, Iizuka, Kunihiko, Ishizuka, Tamotsu, Minato, Koichi, Suda, Satoshi, Kagamu, Hiroshi, Mori, Keita, Kuji, Ichiei, Seki, Nobuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276827/
https://www.ncbi.nlm.nih.gov/pubmed/35821395
http://dx.doi.org/10.1038/s41598-022-15964-3
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author Yamaguchi, Ou
Kaira, Kyoichi
Naruse, Ichiro
Umeda, Yukihiro
Honda, Takeshi
Watanabe, Satoshi
Ichikawa, Kosuke
Tateishi, Kazunari
Kasahara, Norimitsu
Higuchi, Tetsuya
Hashimoto, Kosuke
Shinomiya, Shun
Miura, Yu
Shiono, Ayako
Mouri, Atsuto
Imai, Hisao
Iizuka, Kunihiko
Ishizuka, Tamotsu
Minato, Koichi
Suda, Satoshi
Kagamu, Hiroshi
Mori, Keita
Kuji, Ichiei
Seki, Nobuhiko
author_facet Yamaguchi, Ou
Kaira, Kyoichi
Naruse, Ichiro
Umeda, Yukihiro
Honda, Takeshi
Watanabe, Satoshi
Ichikawa, Kosuke
Tateishi, Kazunari
Kasahara, Norimitsu
Higuchi, Tetsuya
Hashimoto, Kosuke
Shinomiya, Shun
Miura, Yu
Shiono, Ayako
Mouri, Atsuto
Imai, Hisao
Iizuka, Kunihiko
Ishizuka, Tamotsu
Minato, Koichi
Suda, Satoshi
Kagamu, Hiroshi
Mori, Keita
Kuji, Ichiei
Seki, Nobuhiko
author_sort Yamaguchi, Ou
collection PubMed
description Anti-programmed death-1 (PD-1) blockade is a standard treatment for advanced non-small-cell lung cancer (NSCLC). However, no appropriate modality exists for monitoring its therapeutic response immediately after initiation. Therefore, we aimed to elucidate the clinical relevance of (18)F-FDG PET/CT versus CT in predicting the response to PD-1 blockade in the early phase. This prospective study included a total of 54 NSCLC patients. (18)F-FDG PET/CT was performed at 4 weeks and 9 weeks after PD-1 blockade monotherapy. Maximum standardized uptake values (SUL(max)), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were evaluated. Among all patients, partial metabolic response and progressive metabolic disease after PD-1 blockade were observed in 35.2% and 11.1% on SUL(max), 22.2% and 51.8% on MTV, and 27.8% and 46.3% on TLG, respectively, whereas a partial response (PR) and progressive disease (PD), respectively, based on RECIST v1.1 were recognized in 35.2% and 35.2%, respectively. The predictive probability of PR (MTV: 57.9% vs. 21.1%, p = 0.044; TLG: 63.2% vs. 21.1%, p = 0.020) and PD (MTV: 78.9% vs. 47.3%, p = 0.002; TLG: 73.7% vs. 21.1%, p = 0.007) detected based on RECIST at 4 weeks after PD-1 blockade initiation was significantly higher using MTV or TLG on (18)F-FDG uptake than on CT. Multivariate analysis revealed that metabolic response by MTV or TLG at 4 weeks was an independent factor for response to PD-1 blockade treatment. Metabolic assessment by MTV or TLG was superior to morphological changes on CT for predicting the therapeutic response and survival at 4 weeks after PD-1 blockade.
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spelling pubmed-92768272022-07-14 Prospective assessment using (18)F-FDG PET/CT as a novel predictor for early response to PD-1 blockade in non-small-cell lung cancer Yamaguchi, Ou Kaira, Kyoichi Naruse, Ichiro Umeda, Yukihiro Honda, Takeshi Watanabe, Satoshi Ichikawa, Kosuke Tateishi, Kazunari Kasahara, Norimitsu Higuchi, Tetsuya Hashimoto, Kosuke Shinomiya, Shun Miura, Yu Shiono, Ayako Mouri, Atsuto Imai, Hisao Iizuka, Kunihiko Ishizuka, Tamotsu Minato, Koichi Suda, Satoshi Kagamu, Hiroshi Mori, Keita Kuji, Ichiei Seki, Nobuhiko Sci Rep Article Anti-programmed death-1 (PD-1) blockade is a standard treatment for advanced non-small-cell lung cancer (NSCLC). However, no appropriate modality exists for monitoring its therapeutic response immediately after initiation. Therefore, we aimed to elucidate the clinical relevance of (18)F-FDG PET/CT versus CT in predicting the response to PD-1 blockade in the early phase. This prospective study included a total of 54 NSCLC patients. (18)F-FDG PET/CT was performed at 4 weeks and 9 weeks after PD-1 blockade monotherapy. Maximum standardized uptake values (SUL(max)), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were evaluated. Among all patients, partial metabolic response and progressive metabolic disease after PD-1 blockade were observed in 35.2% and 11.1% on SUL(max), 22.2% and 51.8% on MTV, and 27.8% and 46.3% on TLG, respectively, whereas a partial response (PR) and progressive disease (PD), respectively, based on RECIST v1.1 were recognized in 35.2% and 35.2%, respectively. The predictive probability of PR (MTV: 57.9% vs. 21.1%, p = 0.044; TLG: 63.2% vs. 21.1%, p = 0.020) and PD (MTV: 78.9% vs. 47.3%, p = 0.002; TLG: 73.7% vs. 21.1%, p = 0.007) detected based on RECIST at 4 weeks after PD-1 blockade initiation was significantly higher using MTV or TLG on (18)F-FDG uptake than on CT. Multivariate analysis revealed that metabolic response by MTV or TLG at 4 weeks was an independent factor for response to PD-1 blockade treatment. Metabolic assessment by MTV or TLG was superior to morphological changes on CT for predicting the therapeutic response and survival at 4 weeks after PD-1 blockade. Nature Publishing Group UK 2022-07-12 /pmc/articles/PMC9276827/ /pubmed/35821395 http://dx.doi.org/10.1038/s41598-022-15964-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yamaguchi, Ou
Kaira, Kyoichi
Naruse, Ichiro
Umeda, Yukihiro
Honda, Takeshi
Watanabe, Satoshi
Ichikawa, Kosuke
Tateishi, Kazunari
Kasahara, Norimitsu
Higuchi, Tetsuya
Hashimoto, Kosuke
Shinomiya, Shun
Miura, Yu
Shiono, Ayako
Mouri, Atsuto
Imai, Hisao
Iizuka, Kunihiko
Ishizuka, Tamotsu
Minato, Koichi
Suda, Satoshi
Kagamu, Hiroshi
Mori, Keita
Kuji, Ichiei
Seki, Nobuhiko
Prospective assessment using (18)F-FDG PET/CT as a novel predictor for early response to PD-1 blockade in non-small-cell lung cancer
title Prospective assessment using (18)F-FDG PET/CT as a novel predictor for early response to PD-1 blockade in non-small-cell lung cancer
title_full Prospective assessment using (18)F-FDG PET/CT as a novel predictor for early response to PD-1 blockade in non-small-cell lung cancer
title_fullStr Prospective assessment using (18)F-FDG PET/CT as a novel predictor for early response to PD-1 blockade in non-small-cell lung cancer
title_full_unstemmed Prospective assessment using (18)F-FDG PET/CT as a novel predictor for early response to PD-1 blockade in non-small-cell lung cancer
title_short Prospective assessment using (18)F-FDG PET/CT as a novel predictor for early response to PD-1 blockade in non-small-cell lung cancer
title_sort prospective assessment using (18)f-fdg pet/ct as a novel predictor for early response to pd-1 blockade in non-small-cell lung cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276827/
https://www.ncbi.nlm.nih.gov/pubmed/35821395
http://dx.doi.org/10.1038/s41598-022-15964-3
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