Osimertinib-Associated Toxic Epidermal Necrolysis in a Lung Cancer Patient Harboring an EGFR Mutation-A Case Report and a Review of the Literature.
Acrylamides
/ adverse effects
Adenocarcinoma
/ drug therapy
Aged, 80 and over
Aniline Compounds
/ adverse effects
Antineoplastic Agents
/ adverse effects
Asian People
/ genetics
ErbB Receptors
/ genetics
Female
Humans
Immunoglobulins, Intravenous
/ therapeutic use
Lung Neoplasms
/ drug therapy
Mutation
Protein Kinase Inhibitors
/ adverse effects
Stevens-Johnson Syndrome
/ drug therapy
EGFR tyrosine kinase inhibitor
ethnicity
non-small-cell lung cancer
osimertinib
toxic epidermal necrolysis
Journal
Medicina (Kaunas, Lithuania)
ISSN: 1648-9144
Titre abrégé: Medicina (Kaunas)
Pays: Switzerland
ID NLM: 9425208
Informations de publication
Date de publication:
11 Aug 2020
11 Aug 2020
Historique:
received:
12
06
2020
revised:
01
08
2020
accepted:
07
08
2020
entrez:
16
8
2020
pubmed:
17
8
2020
medline:
23
3
2021
Statut:
epublish
Résumé
Toxic epidermal necrolysis (TEN) and Stevens-Johnson syndrome (SJS) are life-threatening dermatologic adverse events in the same category, caused by a delayed-type drug hypersensitivity reaction. Although skin toxicity is common during treatment with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs), osimertinib-associated TEN is quite rare-thus far, only one report has been published from China. We report a case of an 80-year-old Japanese woman with lung adenocarcinoma harboring an EGFR-sensitizing mutation who was treated with osimertinib as the first-line treatment. Forty-six days after osimertinib induction, diffuse erythematous rash rapidly spread over the patient's trunk along with vesicles and purpuric macules; furthermore, she developed targetoid erythema on the face. Despite osimertinib discontinuation and corticosteroid treatment, diffuse erythema with Nikolsky's sign, general epidermal detachment, erosion and loose blisters developed over her entire body including the face. Based on her symptoms, TEN was diagnosed and thus, intravenous immunoglobulin was immediately administered for 4 days. The treatment ameliorated TEN-associated skin toxicity and caused epithelialization. Reports on osimertinib-associated SJS/TEN are scarce and only one report each on SJS and TEN from China is available. This is the first report of osimertinib-associated TEN from Japan. Cases of EGFR-TKI-associated SJS/TEN have been reported predominantly from Asian countries, suggesting ethnicity and genetic linkage play a role in the underlying mechanism.
Identifiants
pubmed: 32796633
pii: medicina56080403
doi: 10.3390/medicina56080403
pmc: PMC7466304
pii:
doi:
Substances chimiques
Acrylamides
0
Aniline Compounds
0
Antineoplastic Agents
0
Immunoglobulins, Intravenous
0
Protein Kinase Inhibitors
0
osimertinib
3C06JJ0Z2O
EGFR protein, human
EC 2.7.10.1
ErbB Receptors
EC 2.7.10.1
Types de publication
Case Reports
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
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