Non-bacterial cystitis with increased expression of programmed death-ligand 1 in the urothelium: An unusual immune-related adverse event during treatment with pembrolizumab for lung adenocarcinoma.

PD‐L1 cystitis immune checkpoint inhibitor immune‐related adverse event

Journal

IJU case reports
ISSN: 2577-171X
Titre abrégé: IJU Case Rep
Pays: Australia
ID NLM: 101764958

Informations de publication

Date de publication:
Nov 2020
Historique:
received: 21 02 2020
revised: 23 06 2020
accepted: 22 07 2020
entrez: 9 11 2020
pubmed: 10 11 2020
medline: 10 11 2020
Statut: epublish

Résumé

Immune checkpoint inhibitors are now a standard therapeutic option for lung adenocarcinoma. However, Immune checkpoint inhibitors often induce various immune-related adverse events. The patient was a 78-year-old woman with lung adenocarcinoma who had a partial response to pembrolizumab. During treatment, she complained of pollakiuria and nocturia with painful micturition. Histological analysis revealed infiltration of CD8-positive and/or TIA-1 cytotoxic granule-associated RNA binding protein-positive lymphocytes and programmed death-ligand 1 expression in the urothelium. A diagnosis of immune-related adverse event cystitis was made based on these clinical and pathological findings. The patient's subjective symptoms and findings on cystoscopy improved dramatically after treatment with prednisolone. Immune checkpoint inhibitors-induced cystitis is extremely rare. This report is the first to include an immunohistochemical analysis of the urothelial epithelium in immune-related adverse event cystitis and describes an instructive case.

Identifiants

pubmed: 33163921
doi: 10.1002/iju5.12211
pii: IJU512211
pmc: PMC7609190
doi:

Types de publication

Case Reports

Langues

eng

Pagination

266-269

Informations de copyright

© 2020 The Authors. IJU Case Reports published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Urological Association.

Déclaration de conflit d'intérêts

K. Matsuo is an employee of Sapporo Clinical Laboratory Inc. The other authors have no conflict of interest in regard to this report.

Références

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pubmed: 29290265
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pubmed: 31730012
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pubmed: 31149494
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pubmed: 29541592
Cell Rep. 2017 May 9;19(6):1189-1201
pubmed: 28494868

Auteurs

Yohei Ueki (Y)

Department of Urology NTT-East Corporation Sapporo Medical Center Sapporo Japan.

Masahiro Matsuki (M)

Department of Urology NTT-East Corporation Sapporo Medical Center Sapporo Japan.

Terufumi Kubo (T)

Department of Pathology School of Medicine Sapporo Medical University Sapporo Japan.

Rena Morita (R)

Department of Pathology School of Medicine Sapporo Medical University Sapporo Japan.

Yoshihiko Hirohashi (Y)

Department of Pathology School of Medicine Sapporo Medical University Sapporo Japan.

Syunsuke Sato (S)

Department of Urology NTT-East Corporation Sapporo Medical Center Sapporo Japan.

Ryota Horibe (R)

Department of Respiratory Medicine NTT-East Corporation Sapporo Medical Center Sapporo Japan.

Kazuhiko Matsuo (K)

Sapporo Clinical Laboratory Inc. Sapporo Japan.

Tomohide Tsukahara (T)

Department of Pathology School of Medicine Sapporo Medical University Sapporo Japan.

Takayuki Kanaseki (T)

Department of Pathology School of Medicine Sapporo Medical University Sapporo Japan.

Yasunari Takakuwa (Y)

Department of Clinical Pathology NTT-East Corporation Sapporo Medical Center Sapporo Hokkaido Japan.

Masaaki Satoh (M)

Department of Clinical Pathology NTT-East Corporation Sapporo Medical Center Sapporo Hokkaido Japan.

Naoki Itoh (N)

Department of Urology NTT-East Corporation Sapporo Medical Center Sapporo Japan.

Toshihiko Torigoe (T)

Department of Pathology School of Medicine Sapporo Medical University Sapporo Japan.

Classifications MeSH