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Systemic Treatment of Metastatic Conjunctival Melanoma

dc.contributor.authorPinto Torres, S
dc.contributor.authorAndré, T
dc.contributor.authorGouveia, E
dc.contributor.authorCosta, L
dc.contributor.authorPassos, MJ
dc.date.accessioned2023-03-01T11:53:52Z
dc.date.available2023-03-01T11:53:52Z
dc.date.issued2017
dc.description.abstractConjunctival melanoma (CM) is an exceptionally rare tumor, with a propensity for local and distant recurrence, with the lungs, skin, liver, and brain being the most common sites of metastasis. Recent progress in systemic treatments, with checkpoint inhibitors and targeted therapies blocking BRAF and MEK, has redefined the standard of care of advanced unresectable and metastatic melanoma. Although most trials did not include patients with conjunctival melanoma, its close molecular and genetic relationship to cutaneous melanoma might suggest a similar response to these novel agents. The authors describe two uncommon cases of metastatic conjunctival melanomas with distinct genetic profiles and, as such, submitted to different systemic treatments.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationCase Rep Oncol Med . 2017;2017:4623964.pt_PT
dc.identifier.doi10.1155/2017/4623964pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4426
dc.language.isoengpt_PT
dc.publisherHindawipt_PT
dc.subjectCHLC OFTpt_PT
dc.subjectConjunctival Melanomapt_PT
dc.titleSystemic Treatment of Metastatic Conjunctival Melanomapt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage3pt_PT
oaire.citation.startPage1pt_PT
oaire.citation.titleCase Reports in Oncological Medicinept_PT
oaire.citation.volume2017pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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