Publication:
New Hopes in Retinoblastoma Treatment

dc.contributor.authorÇEKİÇ, OSMAN
dc.contributor.authorAKKAYA TURHAN, SEMRA
dc.contributor.authorsTurhan, Semra A.; Cekic, Osman
dc.date.accessioned2022-03-10T11:40:20Z
dc.date.accessioned2026-01-10T20:22:50Z
dc.date.available2022-03-10T11:40:20Z
dc.date.issued2014-09-01
dc.description.abstractSurvival rates of retinoblastoma have increased dramatically during the last decade. The current major treatment modalities for retinoblastoma include enucleation, intravenous chemoreduction, external beam therapy, focal treatments (such as brachytherapy and transpupillary thermotherapy), subconjunctival chemotherapy and selective ophthalmic artery chemotherapy. Although current treatment modalities have improved survival rates as well as eye salvage, new treatment modalities are expected to arise in the near future, since above mentioned non-targeted treatments have extensive side effects. Recent advances in genetic analysis of retinoblastoma 1 (RB1) mutations and pathways leading to retinoblastoma may provide vital information for the development of new targeted therapies which are less toxic.
dc.identifier.doi10.4999/uhod.14222
dc.identifier.issn1306-133X
dc.identifier.urihttps://hdl.handle.net/11424/219989
dc.identifier.wosWOS:000342543200009
dc.language.isoeng
dc.publisherAKAD DOKTORLAR YAYINEVI
dc.relation.ispartofUHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectGenetics
dc.subjectRetinoblastoma
dc.subjectRB1 mutation
dc.subjectTargeted treatments
dc.subjectGENOMIC INSTABILITY
dc.subjectTARGETING HYPOXIA
dc.subjectP53 PATHWAY
dc.subjectTUMOR
dc.subjectPROTEIN
dc.subjectPROGRESSION
dc.subjectINHIBITORS
dc.subjectRETINOMA
dc.subjectTHERAPY
dc.subjectP21
dc.titleNew Hopes in Retinoblastoma Treatment
dc.typereview
dspace.entity.typePublication
oaire.citation.endPage207
oaire.citation.issue3
oaire.citation.startPage202
oaire.citation.titleUHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI
oaire.citation.volume24

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