Abstract

BackgroundHerein, we describe the use of systemic immunotherapy for both locally advanced and metastatic conjunctival melanoma. Current treatments for advanced conjunctival melanoma typically result in poor local control leading to disfiguring orbital exenteration surgery. Locoregional spread of conjunctival malignant melanoma typically requires pre-auricular and cervical lymph node dissection with post-operative adjuvant radiation therapy. In addition, classic systemic chemotherapy has been unsuccessful in the treatment of metastatic disease.MethodsThis is a retrospectively analyzed clinical case series of 5 patients with biopsy proven conjunctival melanoma who were treated with checkpoint inhibition therapy. Of these, 3 patients were treated for residual ocular disease present after failing multiple local therapies and refusing orbital exenteration surgery and two (with local ocular control) for metastatic conjunctival melanoma. Both those with locally advanced disease and patients with metastatic disease received an anti-PD1 agent in combination with another immunotherapeutic agent. All 5 were given multiple cycles of systemic anti-PD1 therapy, 1 was initially treated with single agent ipilimumab (3 mg/kg) prior to approval of anti-PD1 agents and two received interferon eye drops. As part of each ophthalmic examination, photographs of all conjunctival and eyelid surfaces were obtained. Systemic evaluations involved initial staging scans as well as periodic re-imaging.ResultsAll cases have shown responses. Of the 2 complete responses, 1 was a patient with systemic disease. No patients developed ocular toxicity or loss of vision. However, systemic adverse effects included adrenal insufficiency, Grade-III colitis, Grade-II dermatitis, Grade-II hepatotoxicity and Grade-II pneumonitis.ConclusionsThis report suggests that systemic immunotherapy with or without topical interferon is effective in treatment of malignant melanoma of the conjunctiva. Therefore, it can be considered for patients with advanced local conjunctival melanoma, those who refuse orbital exenteration surgery and those with systemic metastasis.

Highlights

  • Conjunctival malignant melanoma (CMM) is epidemiologically, molecularly and genetically different from intraocular “uveal” melanoma [1]

  • Conjunctival melanomas eventually grow in a vertical phase, both invading beneath the conjunctival epithelium and develop nodules [1, 4]

  • Ophthalmic examination revealed 20/20 vision, diffuse, multifocal CMM extended onto the cornea, caruncle and eyelid skin (AJCC-T3bN0M0)

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Summary

Introduction

Conjunctival malignant melanoma (CMM) is epidemiologically, molecularly and genetically different from intraocular “uveal” melanoma [1]. More closely related to mucosal melanomas, early stage CMM tend to start as localized, “in situ,” relatively flat and superficial spreading tumors of the epithelium [1, 4]. They commonly extend onto the corneal epithelium and rarely invade the eye. Conjunctival melanomas eventually grow in a vertical phase, both invading beneath the conjunctival epithelium and develop nodules [1, 4] Metastasis to both regional pre-auricular and cervical lymph nodes is Finger and Pavlick Journal for ImmunoTherapy of Cancer (2019) 7:83 typically followed by more widespread systemic disease [4, 5]. Classic systemic chemotherapy has been unsuccessful in the treatment of metastatic disease

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