PD-L1 expression in keratinocyte and infiltration of CD4 + T lymphocyte can predict a severe type of erythema multiforme major induced by the anti-PD-1 antibody, pembrolizumab.

Anti-PD-1 antibody CD8+ T cell Erythema multiforme major PD-L1 expression Severe cutaneous adverse reaction

Journal

International cancer conference journal
ISSN: 2192-3183
Titre abrégé: Int Cancer Conf J
Pays: Singapore
ID NLM: 101734231

Informations de publication

Date de publication:
Jul 2024
Historique:
received: 19 11 2023
accepted: 19 03 2024
medline: 4 7 2024
pubmed: 4 7 2024
entrez: 4 7 2024
Statut: epublish

Résumé

Skin toxicity is the most common adverse event of treatment with immune check point inhibitors. Among them, erythema multiforme is a rare occurrence with a frequency of 4%, with most of the cases developing grade 1/2 disease. We experienced high grade erythema multiforme major developing with pembrolizumab treatment for anal canal cancer with extensive skin metastases. Steroid ointment was ineffective, and the skin lesions with blisters expanded to > 45% of the body surface area. The patient was at risk for symptom aggravation, and a pulse therapy with methylprednisolone and increasing the dose of oral prednisolone (1 mg/kg) were started. The skin lesions improved in 1.8 months. Unless urgent and appropriate treatments such as high dose steroid administration were conducted, the skin toxicities could not be controlled. The presence of CD4 The online version contains supplementary material available at 10.1007/s13691-024-00676-4.

Identifiants

pubmed: 38962048
doi: 10.1007/s13691-024-00676-4
pii: 676
pmc: PMC11217243
doi:

Types de publication

Journal Article

Langues

eng

Pagination

268-274

Informations de copyright

© The Author(s) 2024.

Déclaration de conflit d'intérêts

Conflict of interestThe authors declare that they have no conflict of interest.

Auteurs

Ryohei Kadoi (R)

Department of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.

Taichi Yoshida (T)

Department of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.

Mai Noto (M)

Department of Dermatology and Plastic Surgery, Graduate School of Medicine, Akita University, Akita, Japan.

Aya Toyoshima (A)

Department of Dermatology and Plastic Surgery, Graduate School of Medicine, Akita University, Akita, Japan.

Sino Fujii (S)

Department of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.
Division of Nurse Practitioner, Akita University Hospital, Akita, Japan.

Koji Fukuda (K)

Department of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.

Kazuhiro Shimazu (K)

Department of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.

Daiki Taguchi (D)

Department of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.

Hanae Shinozaki (H)

Department of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.

Naoki Kodama (N)

Department of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.

Michihiro Kono (M)

Department of Dermatology and Plastic Surgery, Graduate School of Medicine, Akita University, Akita, Japan.

Hiroshi Nanjyo (H)

Department of Pathology, Akita University Hospital, Akita, Japan.

Hiroyuki Shibata (H)

Department of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.

Classifications MeSH