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DC Field | Value | Language |
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dc.contributor.author | Prince, Miles | - |
dc.contributor.other | Querfeld, C. | - |
dc.date.accessioned | 2018-10-31T04:34:21Z | - |
dc.date.available | 2018-10-31T04:34:21Z | - |
dc.date.issued | 2018-09 | - |
dc.identifier.citation | Best Pract Res Clin Haematol. 2018 Sep;31(3):322-335. | en_US |
dc.identifier.issn | 1521-6926 | en_US |
dc.identifier.issn | 1532-1924 | en_US |
dc.identifier.uri | http://hdl.handle.net/11434/1548 | - |
dc.description.abstract | Novel 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.publisher | Bailliere Tindall Ltd | en_US |
dc.subject | Novel Systemic Therapies | en_US |
dc.subject | Advanced-Stage Disease | en_US |
dc.subject | Early-Stage Disease | en_US |
dc.subject | Skin-Directed Therapies | en_US |
dc.subject | Systemic Chemotherapy | en_US |
dc.subject | Biological Agents | en_US |
dc.subject | Interferon Alfa | en_US |
dc.subject | Bexarotene | en_US |
dc.subject | Histone Deacetylase Inhibitors | en_US |
dc.subject | Brentuximab Vedotin | en_US |
dc.subject | Mogamulizumab | en_US |
dc.subject | Extracorporeal Photopheresis | en_US |
dc.subject | Sézary Syndrome | en_US |
dc.subject | Allogeneic Transplantation | en_US |
dc.subject | Novel Agents | en_US |
dc.subject | Monoclonal Antibody IPH4102 | en_US |
dc.subject | Duvelisib | en_US |
dc.subject | Denileukin Diftitox | en_US |
dc.subject | Patient Factors | en_US |
dc.subject | Efficacy | en_US |
dc.subject | Toxicity | en_US |
dc.subject | Biological Agents | en_US |
dc.subject | Lymphoma | en_US |
dc.subject | Cutaneous | en_US |
dc.subject | Cancer Services Clinical Institute, Epworth HealthCare, Victoria, Australia | en_US |
dc.title | Integrating novel systemic therapies for the treatment of mycosis fungoides and Sézary syndrome. | en_US |
dc.type | Journal Article | en_US |
dc.identifier.doi | 10.1016/j.beha.2018.07.007 | en_US |
dc.identifier.journaltitle | Best Practice & Research Clinical Haematology | en_US |
dc.description.pubmeduri | https://www.ncbi.nlm.nih.gov/pubmed/30213403 | en_US |
dc.description.affiliates | Sir Peter MacCallum Department of Oncology, University of Melbourne, Victoria, Australia | en_US |
dc.description.affiliates | City of Hope National Medical Center, Beckman Research Institute, California, USA | en_US |
dc.type.studyortrial | Review | en_US |
dc.type.contenttype | Text | en_US |
Appears in Collections: | Cancer Services |
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