Intravitreous Cutaneous Metastatic Melanoma in the Era of Checkpoint Inhibition: Unmasking and Masquerading.


Journal

Ophthalmology
ISSN: 1549-4713
Titre abrégé: Ophthalmology
Pays: United States
ID NLM: 7802443

Informations de publication

Date de publication:
02 2020
Historique:
received: 07 07 2019
revised: 10 09 2019
accepted: 17 09 2019
pubmed: 12 11 2019
medline: 13 6 2020
entrez: 12 11 2019
Statut: ppublish

Résumé

Cutaneous melanoma metastatic to the vitreous is very rare. This study investigated the clinical findings, treatment, and outcome of patients with metastatic cutaneous melanoma to the vitreous. Most patients received checkpoint inhibition for the treatment of systemic disease, and the significance of this was explored. Multicenter, retrospective cohort study. Fourteen eyes of 11 patients with metastatic cutaneous melanoma to the vitreous. Clinical records, including fundus photography and ultrasound results, were reviewed retrospectively, and relevant data were recorded for each patient eye. Clinical features at presentation, ophthalmic and systemic treatments, and outcomes. The median age at presentation of ophthalmic disease was 66 years (range, 23-88 years), and the median follow-up from diagnosis of ophthalmic disease was 23 months. Ten of 11 patients were treated with immune checkpoint inhibition at some point in the treatment course. The median time from starting immunotherapy to ocular symptoms was 17 months (range, 4.5-38 months). Half of eyes demonstrated amelanotic vitreous debris. Five eyes demonstrated elevated intraocular pressure, and 4 eyes demonstrated a retinal detachment. Six patients showed metastatic disease in the central nervous system. Ophthalmic treatment included external beam radiation (30-40 Gy) in 6 eyes, intravitreous melphalan (10-20 μg) in 4 eyes, enucleation of 1 eye, and local observation while receiving systemic treatment in 2 eyes. Three eyes received intravitreous bevacizumab for neovascularization. The final Snellen visual acuity ranged from 20/20 to no light perception. The differential diagnosis of vitreous debris in the context of metastatic cutaneous melanoma includes intravitreal metastasis, and this seems to be particularly apparent during this era of treatment with checkpoint inhibition. External beam radiation, intravitreous melphalan, and systemic checkpoint inhibition can be used in the treatment of ophthalmic disease. Neovascular glaucoma and retinal detachments may occur, and most eyes show poor visual potential. Approximately one quarter of patients demonstrated ocular disease that preceded central nervous system metastasis. Patients with visual symptoms or vitreous debris in the context of metastatic cutaneous melanoma would benefit from evaluation by an ophthalmic oncologist.

Identifiants

pubmed: 31708274
pii: S0161-6420(19)32085-8
doi: 10.1016/j.ophtha.2019.09.018
pmc: PMC7003537
mid: NIHMS1543224
pii:
doi:

Substances chimiques

Antineoplastic Agents, Alkylating 0
Melphalan Q41OR9510P

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

240-248

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

Copyright © 2019 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.

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Auteurs

Jasmine H Francis (JH)

Ophthalmic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, New York; Weill Cornell Medical Center, New York, New York. Electronic address: francij1@mskcc.org.

Duncan Berry (D)

Department of Ophthalmology, Emory University School of Medicine, Atlanta, Georgia.

David H Abramson (DH)

Ophthalmic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, New York; Weill Cornell Medical Center, New York, New York.

Christopher A Barker (CA)

Weill Cornell Medical Center, New York, New York; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.

Chris Bergstrom (C)

Retina Consultants of Carolina, Greenville, South Carolina.

Hakan Demirci (H)

Department of Ophthalmology and Visual Sciences, Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan.

Michael Engelbert (M)

Vitreous Retina Macula Consultant of New York, New York, New York; Department of Ophthalmology, New York University Langone Health, New York, New York.

Hans Grossniklaus (H)

Department of Ophthalmology, Emory University School of Medicine, Atlanta, Georgia.

Baker Hubbard (B)

Department of Ophthalmology, Emory University School of Medicine, Atlanta, Georgia.

Codrin E Iacob (CE)

Department of Pathology, The New York Eye and Ear Infirmary of Mount Sinai, New York, New York.

Korey Jaben (K)

Ophthalmic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, New York; Weill Cornell Medical Center, New York, New York.

Madhavi Kurli (M)

Advanced Retina & Eye Cancer Center, Phoenix, Arizona.

Michael A Postow (MA)

Weill Cornell Medical Center, New York, New York; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Jedd D Wolchok (JD)

Weill Cornell Medical Center, New York, New York; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Ivana K Kim (IK)

Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts.

Jill R Wells (JR)

Department of Ophthalmology, Emory University School of Medicine, Atlanta, Georgia.

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Classifications MeSH