Medical treatment for ocular surface squamous neoplasia

David Monroy1, Andres Serrano2, Anat Galor1,3

  • 1Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, USA.

Eye (London, England)
|February 8, 2023
PubMed

Insights

Topical medications like interferon alpha-2b and 5-fluorouracil are effective first-line treatments for ocular surface squamous neoplasia (OSSN). Mitomycin C is a second-line option, while newer agents show promise for OSSN management.

Area of Science:

  • Ophthalmology
  • Oncology
  • Dermatology

Background:

  • Ocular surface squamous neoplasia (OSSN) is the most common non-melanoma tumor affecting the eye's surface.
  • Historically, surgical excision was the primary treatment, but topical therapies have emerged as effective alternatives.
  • Advancements in diagnostic tools like high-resolution optical coherence tomography (HR-OCT) aid in OSSN detection and monitoring.

Purpose of the Study:

  • To provide an updated literature review on medical treatments for OSSN.
  • To compare the efficacy and safety profiles of various topical agents for OSSN.
  • To discuss emerging therapies for OSSN.

Main Methods:

  • Literature review of medical treatments for OSSN.
  • Analysis of topical agents including interferon alpha-2b (IFNα-2b), 5-fluorouracil (5-FU), and mitomycin C (MMC).
  • Exploration of newer agents like immune checkpoint inhibitors, retinoic acid, and anti-VEGF therapies.

Main Results:

  • Interferon alpha-2b (IFNα-2b) and 5-fluorouracil (5-FU) are effective and well-tolerated first-line topical treatments for OSSN.
  • Mitomycin C (MMC) is effective but considered a second-line option due to its toxicity.
  • Emerging agents demonstrate potential anti-neoplastic properties for OSSN treatment.

Conclusions:

  • Topical medications offer a viable and often preferred alternative to surgery for OSSN.
  • The choice of topical agent depends on efficacy, side effect profile, and treatment line.
  • Further research into newer agents may expand therapeutic options for OSSN.

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