In a study of vemurafenib recipients, about 10% were referred for ocular symptoms.
Although various adverse effects have been associated with vemurafenib and dabrafenib treatment of advanced melanoma, ocular symptoms have not been reported in the literature. Uveitis can now be added to a long list of potential complications resulting from selective BRAF inhibitors.
To characterize the risk for developing uveitis and its effects in vemurafenib recipients, these researchers collected data on metastatic melanoma patients referred for ocular symptoms (pain, redness, vision loss, blurred vision, and floaters) to a French department of ophthalmology. Eight of 78 vemurafenib recipients were referred for ocular symptoms, and 7 received a uveitis diagnosis. Time from treatment initiation to symptom onset ranged from 3 weeks to 7 mo…
Reviewing Author
DisclosuresConsultant / advisory board Lubax; WorldCare Clinical
EquityLubax
Grant / Research support NIH; Department of Defense; American Skin Association; Piramal
Editorial boardsBritish Journal of Dermatology; Journal of the American Academy of Dermatology; Journal of Investigative Dermatology
Leadership positions in professional societies American Academy of Dermatology (Chair, Skin Cancer and Melanoma Committee); American Board of Dermatology (Director)
DisclosuresConsultant / advisory board Lubax; WorldCare Clinical
EquityLubax
Grant / Research support NIH; Department of Defense; American Skin Association; Piramal
Editorial boardsBritish Journal of Dermatology; Journal of the American Academy of Dermatology; Journal of Investigative Dermatology
Leadership positions in professional societies American Academy of Dermatology (Chair, Skin Cancer and Melanoma Committee); American Board of Dermatology (Director)