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Serum Antibody Against NY-ESO-1 and XAGE1 Antigens Potentially Predicts Clinical Responses to Anti–Programmed Cell Death-1 Therapy in NSCLC

https://hiroshima.repo.nii.ac.jp/records/2007564
https://hiroshima.repo.nii.ac.jp/records/2007564
c85ef18f-ebda-47a4-a9a5-fd1b60ece0d7
名前 / ファイル ライセンス アクション
JThoracOncol_14_2071.pdf JThoracOncol_14_2071.pdf (889.0 KB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル Serum Antibody Against NY-ESO-1 and XAGE1 Antigens Potentially Predicts Clinical Responses to Anti–Programmed Cell Death-1 Therapy in NSCLC
言語 en
作成者 Ohue, Yoshihiro

× Ohue, Yoshihiro

en Ohue, Yoshihiro

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Kurose, Koji

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en Kurose, Koji

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Karasaki, Takahiro

× Karasaki, Takahiro

en Karasaki, Takahiro

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Isobe, Midori

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en Isobe, Midori

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Yamaoka, Takaaki

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en Yamaoka, Takaaki

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Futami, Junichiro

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en Futami, Junichiro

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Irei, Isao

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en Irei, Isao

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Masuda, Takeshi

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en Masuda, Takeshi

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Fukuda, Masaaki

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Kinoshita, Akitoshi

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Matsushita, Hirokazu

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Shimizu, Katsuhiko

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Nakata, Masao

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Hattori, Noboru

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Yamaguchi, Hiroyuki

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Fukuda, Minoru

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Nozawa, Ryohei

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Kakimi, Kazuhiro

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Oka, Mikio

× Oka, Mikio

en Oka, Mikio

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
権利情報 © 2019 International Association for the Study of Lung Cancer. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).
主題
主題Scheme Other
主題 Biomarker
主題
主題Scheme Other
主題 Anti–programmed death 1 therapy
主題
主題Scheme Other
主題 NSCLC
主題
主題Scheme Other
主題 Cancer-testis antigen
主題
主題Scheme Other
主題 Serum antibody
内容記述
内容記述 Introduction: Programmed cell death-1 (PD-1) inhibitors effectively treat NSCLC and prolong survival. Robust biomarkers for predicting clinical benefits of good response and long survival with anti–PD-1 therapy have yet to be identified; therefore, predictive biomarkers are needed to select patients with benefits. Methods: We conducted a prospective study to explore whether serum antibody against NY-ESO-1 and/or XAGE1 cancer-testis antigens predicted primarily good clinical response and secondarily long survival with anti–PD-1 therapy for NSCLC. The serum antibody was detected by enzyme-linked immunosorbent assay, and tumor immune microenvironment and mutation burden were analyzed by immunohistochemistry and next-generation sequencing. Results: In the discovery cohort (n ¼ 13), six antibodypositive NSCLC cases responded to anti–PD-1 therapy (two complete and four partial responses), whereas seven antibody-negative NSCLC cases did not. Antibody positivity was associated with good response and survival, regardless of tumor programmed death ligand 1 (PD-L1) expression, mutation burden, and CD8þ T-cell infiltration. In the validation cohort (n ¼ 75), 17 antibody-positive NSCLC cases responded well to anti–PD-1 therapy as compared with 58 negative NSCLC cases (objective response rate 65% versus 19%, p ¼ 0.0006) and showed significantly prolonged progression-free survival and overall survival. Antibody titers highly correlated with tumor reduction rates. In the multivariate analysis, response biomarkers were tumor programmed death ligand 1 expression and antibody positivity, and only antibody positivity was a significantly better predictive biomarker of progression-free survival (hazard ratio ¼ 0.4, p ¼ 0.01) and overall survival (hazard ratio ¼ 0.2, p ¼ 0.004). Conclusions: Our results suggest that NY-ESO-1 and/or XAGE1 serum antibodies are useful biomarkers for predicting clinical benefits in anti–PD-1 therapy for NSCLC and probably for other cancers.
言語 en
内容記述
内容記述タイプ Other
内容記述 This work was supported by grants from JSPS KAKENHI (15K09235, 16K18463, 16K21533, 18K15226, and 18K07306) to Drs. Oka, Ohue, and Kurose; by grants from the Takeda Science Foundation to Drs. Ohue and Kurose; by a grant from the Medical Research Encouragement Prize of The Japan Medical Association to Dr. Ohue; by a grant from the Okayama Health Foundation to Dr. Ohue; and by grants from Kawasaki Medical School to Drs. Oka, Ohue, and Kurose. Dr. Oka received collaborative research funds from the University of Tokyo and Thyas Co., Ltd. The Department of Immuno-Oncology is endowed by Pole Star Co., Ltd.
出版者
出版者 International Association for the Study of Lung Cancer
出版者
出版者 Elsevier
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連情報
識別子タイプ DOI
関連識別子 10.1016/j.jtho.2019.08.008
関連情報
識別子タイプ PMID
関連識別子 31449889
関連情報
識別子タイプ DOI
関連識別子 https://doi.org/10.1016/j.jtho.2019.08.008
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 1556-0864
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 1556-1380
開始ページ
開始ページ 2071
書誌情報 Journal of Thoracic Oncology
Journal of Thoracic Oncology

巻 14, 号 12, p. 2071-2083, 発行日 2019-12
旧ID 48637
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