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  1. C100 医学部/医学系研究科
  2. C100a 雑誌掲載論文
  3. 学術雑誌

Biomarkers for immune-related adverse events in cancer patients treated with immune checkpoint inhibitors

http://hdl.handle.net/2237/0002010870
http://hdl.handle.net/2237/0002010870
beebe0bf-ae56-4a44-aa85-889a72fa85b1
名前 / ファイル ライセンス アクション
irAE_manuscript_accepted_version.pdf irAE_manuscript_accepted_version.pdf (426 KB)
Table1.pdf Table1.pdf (153 KB)
Table2.pdf Table2.pdf (224 KB)
Figure Figure 1.pdf (232 KB)
アイテムタイプ itemtype_ver1(1)
公開日 2024-05-24
タイトル
タイトル Biomarkers for immune-related adverse events in cancer patients treated with immune checkpoint inhibitors
言語 en
著者 Liang, Yao

× Liang, Yao

en Liang, Yao

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Maeda, Osamu

× Maeda, Osamu

en Maeda, Osamu

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Ando, Yuichi

× Ando, Yuichi

en Ando, Yuichi

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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
権利情報 This is a pre-copyedited, author-produced version of an article accepted for publication in [Japanese Journal of Clinical Oncology] following peer review. The version of record [Yao Liang, Osamu Maeda, Yuichi Ando, Biomarkers for immune-related adverse events in cancer patients treated with immune checkpoint inhibitors, Japanese Journal of Clinical Oncology, Volume 54, Issue 4, April 2024, Pages 365–375, https://doi.org/10.1093/jjco/hyad184] is available online at: https://doi.org/10.1093/jjco/hyad184.
言語 en
内容記述
内容記述タイプ Abstract
内容記述 Although immune checkpoint inhibitors have greatly improved cancer therapy, they also cause immune-related adverse events, including a wide range of inflammatory side effects resulting from excessive immune activation. Types of immune-related adverse events are diverse and can occur in almost any organ, with different frequencies and severities. Furthermore, immune-related adverse events may occur within the first few weeks after treatment or even several months after treatment discontinuation. Predictive biomarkers include blood cell counts and cell surface markers, serum proteins, autoantibodies, cytokines/chemokines, germline genetic variations and gene expression profiles, human leukocyte antigen genotype, microRNAs and the gut microbiome. Given the inconsistencies in research results and limited practical utility, there is to date no established biomarker that can be used in routine clinical practice, and additional investigations are essential to demonstrate efficacy and subsequently facilitate integration into routine clinical use.
言語 en
出版者
出版者 Oxford University Press
言語 en
言語
言語 eng
資源タイプ
資源タイプresource http://purl.org/coar/resource_type/c_6501
タイプ journal article
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
関連情報
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1093/jjco/hyad184
収録物識別子
収録物識別子タイプ EISSN
収録物識別子 1465-3621
書誌情報 en : Japanese Journal of Clinical Oncology

巻 54, 号 4, p. 365-375, 発行日 2024-04
ファイル公開日
日付 2024-10-01
日付タイプ Available
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