Please use this identifier to cite or link to this item: http://hdl.handle.net/11434/1548
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dc.contributor.authorPrince, Miles-
dc.contributor.otherQuerfeld, C.-
dc.date.accessioned2018-10-31T04:34:21Z-
dc.date.available2018-10-31T04:34:21Z-
dc.date.issued2018-09-
dc.identifier.citationBest Pract Res Clin Haematol. 2018 Sep;31(3):322-335.en_US
dc.identifier.issn1521-6926en_US
dc.identifier.issn1532-1924en_US
dc.identifier.urihttp://hdl.handle.net/11434/1548-
dc.description.abstractNovel systemic therapies are generally prescribed to patients with advanced-stage disease or those with early-stage disease refractory to skin-directed therapies. In general, systemic chemotherapy should be reserved for patients who fail to respond to biological agents. Such biological agents include interferon alfa, bexarotene, histone deacetylase inhibitors (vorinostat, romidepsin), brentuximab vedotin and mogamulizumab. Extracorporeal photopheresis is particularly effective for patients with Sézary Syndrome. Allogeneic transplantation is becoming increasing used for younger patients. Novel agents in advanced development include the monoclonal antibody IPH4102,duvelisib,and the new modified formulation of denileukin diftitox. The choice of agents for patients is typically a balance of patient factors (age, co-morbidities, geographic location), relative efficacy and toxicity.en_US
dc.publisherBailliere Tindall Ltden_US
dc.subjectNovel Systemic Therapiesen_US
dc.subjectAdvanced-Stage Diseaseen_US
dc.subjectEarly-Stage Diseaseen_US
dc.subjectSkin-Directed Therapiesen_US
dc.subjectSystemic Chemotherapyen_US
dc.subjectBiological Agentsen_US
dc.subjectInterferon Alfaen_US
dc.subjectBexaroteneen_US
dc.subjectHistone Deacetylase Inhibitorsen_US
dc.subjectBrentuximab Vedotinen_US
dc.subjectMogamulizumaben_US
dc.subjectExtracorporeal Photopheresisen_US
dc.subjectSézary Syndromeen_US
dc.subjectAllogeneic Transplantationen_US
dc.subjectNovel Agentsen_US
dc.subjectMonoclonal Antibody IPH4102en_US
dc.subjectDuvelisiben_US
dc.subjectDenileukin Diftitoxen_US
dc.subjectPatient Factorsen_US
dc.subjectEfficacyen_US
dc.subjectToxicityen_US
dc.subjectBiological Agentsen_US
dc.subjectLymphomaen_US
dc.subjectCutaneousen_US
dc.subjectCancer Services Clinical Institute, Epworth HealthCare, Victoria, Australiaen_US
dc.titleIntegrating novel systemic therapies for the treatment of mycosis fungoides and Sézary syndrome.en_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.beha.2018.07.007en_US
dc.identifier.journaltitleBest Practice & Research Clinical Haematologyen_US
dc.description.pubmedurihttps://www.ncbi.nlm.nih.gov/pubmed/30213403en_US
dc.description.affiliatesSir Peter MacCallum Department of Oncology, University of Melbourne, Victoria, Australiaen_US
dc.description.affiliatesCity of Hope National Medical Center, Beckman Research Institute, California, USAen_US
dc.type.studyortrialReviewen_US
dc.type.contenttypeTexten_US
Appears in Collections:Cancer Services

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