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ID 69580
フルテキストURL
fulltext.pdf 1.15 MB
著者
Ikeda, Daisuke Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Nawada, Tomohiro The Center for Graduate Medical Education, Okayama University Hospital
Kondo, Takumi Department of Hematology and Oncology, Okayama University Hospital
Shinohara, Takayuki Department of Fungal Infection, National Institute of Infectious Diseases
Nagano, Tomohiro Department of Hematology and Oncology, Okayama University Hospital
Kubota, Saya Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Hiyama, Ryuichiro Department of Hematology and Oncology, Okayama University Hospital
Ueno, Masaya Department of Hematology and Oncology, Okayama University Hospital
Kobayashi, Hiroki Department of Hematology and Oncology, Okayama University Hospital
Seike, Keisuke Department of Hematology and Oncology, Okayama University Hospital
Fujiwara, Hideaki Department of Hematology and Oncology, Okayama University Hospital
Asada, Noboru Department of Hematology and Oncology, Okayama University Hospital Kaken ID researchmap
Ennishi, Daisuke Department of Hematology and Oncology, Okayama University Hospital
Fujii, Keiko Department of Hematology and Oncology, Okayama University Hospital Kaken ID researchmap
Fujii, Nobuharu Department of Hematology and Oncology, Okayama University Hospital Kaken ID publons researchmap
Makita, Masanori Department of Hematology, Chugoku Central Hospital
Maeda, Yoshinobu Department of Hematology and Oncology, Okayama University Hospital Kaken ID researchmap
抄録
Introduction: Invasive fungal infection (IFI) after chimeric antigen receptor (CAR) T-cell therapy is less common than bacterial and viral infections, but can be fatal once it develops. As most cases occur within 30 days after CAR T-cell infusion, late-onset IFI—particularly mould infection—appears to be under-recognised.
Discussion: We report an illustrative case of pituitary aspergillosis developing as late as one year after CD19 CAR T-cell therapy, highlighting a persistent risk in certain patients with delayed immune reconstitution.
Conclusion: This case underscores the need for continued vigilance and individualised antifungal strategies to prevent IFI beyond the early post-infusion period.
Trial Registration: The authors have confirmed clinical trial registration is not needed for this submission.
キーワード
aspergillosis
CD19 CAR T
invasive fungal infection
pituitary
発行日
2025-09-02
出版物タイトル
eJHaem
6巻
5号
出版者
Wiley
開始ページ
e70138
ISSN
2688-6146
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2025 The Author(s).
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1002/jha2.70138
ライセンス
http://creativecommons.org/licenses/by/4.0/
Citation
D. Ikeda, T. Nawada, T. Kondo, et al. “ Late-Onset Invasive Aspergillosis With Pituitary Involvement and Dysfunction Following CD19 Chimeric Antigen Receptor T-Cell Therapy.” eJHaem 6, no. 5 (2025): 6, e70138. https://doi.org/10.1002/jha2.70138