Diffuse lichen planus-like keratoses and clinical pseudo-progression associated with avelumab treatment for Merkel cell carcinoma, a case report.
Aged
Antibodies, Monoclonal
/ administration & dosage
Antibodies, Monoclonal, Humanized
Antineoplastic Agents
/ administration & dosage
B7-H1 Antigen
/ antagonists & inhibitors
Carcinoma, Merkel Cell
/ drug therapy
Cryotherapy
Disease Progression
Glucocorticoids
/ therapeutic use
Humans
Keratosis
/ drug therapy
Lichen Planus
/ pathology
Male
Positron Emission Tomography Computed Tomography
Programmed Cell Death 1 Receptor
/ antagonists & inhibitors
Skin Neoplasms
/ drug therapy
Treatment Outcome
Triamcinolone
/ therapeutic use
Drug reactions
Immune checkpoint
Immunology
Lichen planus-like keratosis
Merkel cell
Journal
BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800
Informations de publication
Date de publication:
04 Jun 2019
04 Jun 2019
Historique:
received:
01
05
2018
accepted:
27
05
2019
entrez:
6
6
2019
pubmed:
6
6
2019
medline:
18
12
2019
Statut:
epublish
Résumé
Avelumab is an anti-programmed cell death ligand 1 (PD-L1) antibody approved for treatment of Merkel cell carcinoma (MCC) and locally advanced or metastatic urothelial carcinoma. It shares a similar side effect profile to other immune checkpoint inhibitors, including immune-related adverse reactions in the skin. These adverse skin reactions can present as a morbilliform exanthem, lichenoid dermatitis, vitiligo, autoimmune bullous disorder, among others. We describe a patient with advanced MCC successfully treated with avelumab who developed acute onset diffuse lichen planus-like keratoses (LPLK) at sites of existing seborrheic keratoses (SK) and lentigines. Histopathology of an affected SK revealed papillomatous epidermal hyperplasia with lichenoid interface changes, numerous dyskeratotic keratinocytes and intermittent hypergranulosis. The findings resembled lichen planus (LP) arising in an SK. Onset of the skin symptoms corresponded with an inflammatory cancer response (clinical pseudo-progression), and the eruption improved as overall tumor burden decreased. The patient's pruritus was treated with topical steroids and cyrotherapy for individual symptomatic lesions. Diffuse LPLK is a distinct immune-related reaction pattern associated with PD-L1/PD-1 checkpoint blockade. This is an important side effect to be aware of as LPLK frequently mimic keratinocytic neoplasms. Further observation is needed to assess the prevalence and significance of this immune therapy-associated adverse reaction.
Sections du résumé
BACKGROUND
BACKGROUND
Avelumab is an anti-programmed cell death ligand 1 (PD-L1) antibody approved for treatment of Merkel cell carcinoma (MCC) and locally advanced or metastatic urothelial carcinoma. It shares a similar side effect profile to other immune checkpoint inhibitors, including immune-related adverse reactions in the skin. These adverse skin reactions can present as a morbilliform exanthem, lichenoid dermatitis, vitiligo, autoimmune bullous disorder, among others.
CASE PRESENTATION
METHODS
We describe a patient with advanced MCC successfully treated with avelumab who developed acute onset diffuse lichen planus-like keratoses (LPLK) at sites of existing seborrheic keratoses (SK) and lentigines. Histopathology of an affected SK revealed papillomatous epidermal hyperplasia with lichenoid interface changes, numerous dyskeratotic keratinocytes and intermittent hypergranulosis. The findings resembled lichen planus (LP) arising in an SK. Onset of the skin symptoms corresponded with an inflammatory cancer response (clinical pseudo-progression), and the eruption improved as overall tumor burden decreased. The patient's pruritus was treated with topical steroids and cyrotherapy for individual symptomatic lesions.
CONCLUSION
CONCLUSIONS
Diffuse LPLK is a distinct immune-related reaction pattern associated with PD-L1/PD-1 checkpoint blockade. This is an important side effect to be aware of as LPLK frequently mimic keratinocytic neoplasms. Further observation is needed to assess the prevalence and significance of this immune therapy-associated adverse reaction.
Identifiants
pubmed: 31164102
doi: 10.1186/s12885-019-5759-1
pii: 10.1186/s12885-019-5759-1
pmc: PMC6549366
doi:
Substances chimiques
Antibodies, Monoclonal
0
Antibodies, Monoclonal, Humanized
0
Antineoplastic Agents
0
B7-H1 Antigen
0
CD274 protein, human
0
Glucocorticoids
0
PDCD1 protein, human
0
Programmed Cell Death 1 Receptor
0
Triamcinolone
1ZK20VI6TY
avelumab
KXG2PJ551I
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
539Subventions
Organisme : National Cancer Institute
ID : ZIA BC 011450
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