Eruptive keratoacanthoma secondary to immune checkpoint inhibitors: a narrative review

Layna Mager1, Jose A Plaza2,3, Jennifer Sopkovich2

  • 1The Ohio State University College of Medicine, Columbus, OH, USA.

PubMed

Insights

Eruptive keratoacanthomas (KA) are rare side effects of cancer immunotherapy. Intralesional injections of triamcinolone or methotrexate effectively treated these lesions, offering a less invasive option than surgery.

Area of Science:

  • Dermatology
  • Oncology
  • Immunology

Background:

  • Cancer immunotherapy, particularly immune checkpoint inhibitors, is increasingly used for advanced malignancies.
  • Cutaneous adverse events are common, but rarer effects like eruptive keratoacanthomas (KA) are less understood.
  • Surgical excision is the standard treatment for KA, but less invasive options are sought.

Purpose of the Study:

  • To investigate the efficacy of intralesional injections for treating eruptive keratoacanthomas (KA) secondary to immune checkpoint inhibitor therapy.
  • To review existing literature and present novel case data on this specific adverse event.

Main Methods:

  • A PubMed database search was conducted for cases of eruptive KA linked to immune checkpoint inhibitors.
  • Three additional unpublished cases from the authors' institution were included.
  • Patient data on treatment modalities and outcomes were analyzed.

Main Results:

  • Nineteen patients with immunotherapy-induced eruptive KA were identified (mean age 78.9 years).
  • Treatments included intralesional injections (n=7), systemic agents (n=5), or alternative therapies (n=7).
  • An overall improvement rate of 89.5% was observed, with complete resolution in patients receiving intralesional triamcinolone or methotrexate.

Conclusions:

  • Intralesional injections represent a potentially effective and less invasive treatment for eruptive keratoacanthomas caused by immunotherapy.
  • This approach may allow for the continuation or reinitiation of crucial cancer immunotherapy.
  • Further research into intralesional therapies for managing immune-related adverse events is warranted.

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