Please use this identifier to cite or link to this item: http://hdl.handle.net/11434/2043
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dc.contributor.authorPrince, Miles-
dc.contributor.otherCampbell, Belinda-
dc.contributor.otherRyan, Gail-
dc.contributor.otherMcCormack, Christopher-
dc.contributor.otherTangas, Eleanor-
dc.contributor.otherBressel, Mathias-
dc.contributor.otherTwigger, Robert-
dc.contributor.otherBuelens, Odette-
dc.contributor.othervan der Weyden, Carrie-
dc.date2019-11-
dc.date.accessioned2021-11-23T00:36:51Z-
dc.date.available2021-11-23T00:36:51Z-
dc.date.issued2019-11-
dc.identifier.citationCancers, 11(11), 1758.en_US
dc.identifier.issn2072-6694en_US
dc.identifier.urihttp://hdl.handle.net/11434/2043-
dc.description.abstractMycosis fungoides (MF) and Sezary syndrome (SS) are multi-relapsing, morbid, cutaneous T-cell lymphomas. Optimal treatment sequencing remains undefined. Total skin electron therapy (TSE) is a highly technical, skin-directed treatment, uniquely producing symptom-free and treatment-free intervals. Recent publications favour low-dose TSE for reduced toxicity, but early data support conventional-dose TSE (cdTSE) for longer disease control. Patient selection requires weighing-up tolerability against response durability. We investigated duration of benefit from cdTSE in patients with poorer prognosis diseases: SS and heavily pre-treated MF. Endpoints were overall survival, and “time to next treatment” (TTNT) as surrogate for clinical benefit duration. Seventy patients (53 MF, 17 SS) were eligible: median prior treatments, 4; median cdTSE dose, 30 Gy; median follow-up, 5.8 years. SS patients had worse prognosis (HR = 5.0, p < 0.001) and shorter TTNT (HR = 4.5, p < 0.001) than MF patients; median TTNT was only 3.7 months. Heavily pre-treated MF patients had inferior prognosis (HR = 1.19 per additional line, p = 0.005), and shorter TTNT (HR = 1.13 per additional line, p = 0.031). Median TTNT for MF patients with ≥3 prior treatments was 7.1 months, versus 23.2 months for 0–2 prior treatments. In conclusion, cdTSE has a limited role in SS. TTNT is reduced in heavily pre-treated MF patients, suggesting greater benefit when utilized earlier in treatment sequencing.en_US
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)en_US
dc.subjectDurable Remissionen_US
dc.subjectConventional-Doseen_US
dc.subjectTotal Skin Electron Therapy (TSE)en_US
dc.subjectSezary Syndromeen_US
dc.subjectMultiply Relapsed Mycosis Fungoides (MF)en_US
dc.subjectCutaneous T-cell Lymphomasen_US
dc.subjectConventional-dose TSE (cdTSE)en_US
dc.subjectSymptom Controlen_US
dc.subjectTolerability Against Response Durabilityen_US
dc.subjectOverall Survival (OS)en_US
dc.subjectInferior Prognosisen_US
dc.subjectSkin-Directed Therapyen_US
dc.subjectTime to Next Treatment (TTNT)en_US
dc.subjectSystemic Treatmentsen_US
dc.subjectHaematopoietic Stem Cell Transplantation (HSCT)en_US
dc.subjectHigh-Grade Transformationen_US
dc.subjectAutologous Stem Cell Transplant (SCT)en_US
dc.subjectAllogeneic Haematopoietic SCT (HSCT)en_US
dc.subjectChemotherapyen_US
dc.subjectRotary-Dual Techniqueen_US
dc.subjectSurrogate endpointen_US
dc.subjectEpworth Centre for Immunotherapies and Snowdome Laboratoriesen_US
dc.subjectMolecular Oncology and Cancer Immunologyen_US
dc.subjectCancer Services Clinical Institute, Epworth HealthCare, Victoria, Australiaen_US
dc.titleLack of durable remission with conventional-dose total skin electron therapy for the management of Sezary syndrome and multiple relapsed mycosis fungoides.en_US
dc.typeJournal Articleen_US
dc.identifier.doi10.3390/cancers11111758en_US
dc.identifier.journaltitleCancers (Basel)en_US
dc.description.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/31717353en_US
dc.description.affiliatesDepartment of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne 3000, Victoria, Australiaen_US
dc.description.affiliatesDepartment of Clinical Pathology, The University of Melbourne, Parkville 3010, Victoria, Australiaen_US
dc.description.affiliatesDepartment of Surgical Oncology, Peter MacCallum Cancer Centre, Melbourne 3000, Victoria, Australiaen_US
dc.description.affiliatesDepartment of Dermatology, St Vincent’s Hospital Melbourne, Fitzroy 3065, Victoria, Australiaen_US
dc.description.affiliatesMelbourne Clinical School, School of Medicine, University of Notre Dame, Werribee 3030, Victoria, Australiaen_US
dc.description.affiliatesCentre for Biostatics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne 3000, Victoren_US
dc.description.affiliatesDepartment of Clinical Haematology, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne 3000, Victoria, Australiaen_US
dc.description.affiliatesSir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville 3010, Victoria, Australiaen_US
dc.type.studyortrialClinical Trialen_US
dc.type.contenttypeTexten_US
Appears in Collections:Cancer Services
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