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http://hdl.handle.net/11434/2043
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DC Field | Value | Language |
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dc.contributor.author | Prince, Miles | - |
dc.contributor.other | Campbell, Belinda | - |
dc.contributor.other | Ryan, Gail | - |
dc.contributor.other | McCormack, Christopher | - |
dc.contributor.other | Tangas, Eleanor | - |
dc.contributor.other | Bressel, Mathias | - |
dc.contributor.other | Twigger, Robert | - |
dc.contributor.other | Buelens, Odette | - |
dc.contributor.other | van der Weyden, Carrie | - |
dc.date | 2019-11 | - |
dc.date.accessioned | 2021-11-23T00:36:51Z | - |
dc.date.available | 2021-11-23T00:36:51Z | - |
dc.date.issued | 2019-11 | - |
dc.identifier.citation | Cancers, 11(11), 1758. | en_US |
dc.identifier.issn | 2072-6694 | en_US |
dc.identifier.uri | http://hdl.handle.net/11434/2043 | - |
dc.description.abstract | Mycosis 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.publisher | Multidisciplinary Digital Publishing Institute (MDPI) | en_US |
dc.subject | Durable Remission | en_US |
dc.subject | Conventional-Dose | en_US |
dc.subject | Total Skin Electron Therapy (TSE) | en_US |
dc.subject | Sezary Syndrome | en_US |
dc.subject | Multiply Relapsed Mycosis Fungoides (MF) | en_US |
dc.subject | Cutaneous T-cell Lymphomas | en_US |
dc.subject | Conventional-dose TSE (cdTSE) | en_US |
dc.subject | Symptom Control | en_US |
dc.subject | Tolerability Against Response Durability | en_US |
dc.subject | Overall Survival (OS) | en_US |
dc.subject | Inferior Prognosis | en_US |
dc.subject | Skin-Directed Therapy | en_US |
dc.subject | Time to Next Treatment (TTNT) | en_US |
dc.subject | Systemic Treatments | en_US |
dc.subject | Haematopoietic Stem Cell Transplantation (HSCT) | en_US |
dc.subject | High-Grade Transformation | en_US |
dc.subject | Autologous Stem Cell Transplant (SCT) | en_US |
dc.subject | Allogeneic Haematopoietic SCT (HSCT) | en_US |
dc.subject | Chemotherapy | en_US |
dc.subject | Rotary-Dual Technique | en_US |
dc.subject | Surrogate endpoint | en_US |
dc.subject | Epworth Centre for Immunotherapies and Snowdome Laboratories | en_US |
dc.subject | Molecular Oncology and Cancer Immunology | en_US |
dc.subject | Cancer Services Clinical Institute, Epworth HealthCare, Victoria, Australia | en_US |
dc.title | Lack of durable remission with conventional-dose total skin electron therapy for the management of Sezary syndrome and multiple relapsed mycosis fungoides. | en_US |
dc.type | Journal Article | en_US |
dc.identifier.doi | 10.3390/cancers11111758 | en_US |
dc.identifier.journaltitle | Cancers (Basel) | en_US |
dc.description.pubmeduri | https://pubmed.ncbi.nlm.nih.gov/31717353 | en_US |
dc.description.affiliates | Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne 3000, Victoria, Australia | en_US |
dc.description.affiliates | Department of Clinical Pathology, The University of Melbourne, Parkville 3010, Victoria, Australia | en_US |
dc.description.affiliates | Department of Surgical Oncology, Peter MacCallum Cancer Centre, Melbourne 3000, Victoria, Australia | en_US |
dc.description.affiliates | Department of Dermatology, St Vincent’s Hospital Melbourne, Fitzroy 3065, Victoria, Australia | en_US |
dc.description.affiliates | Melbourne Clinical School, School of Medicine, University of Notre Dame, Werribee 3030, Victoria, Australia | en_US |
dc.description.affiliates | Centre for Biostatics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne 3000, Victor | en_US |
dc.description.affiliates | Department of Clinical Haematology, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne 3000, Victoria, Australia | en_US |
dc.description.affiliates | Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville 3010, Victoria, Australia | en_US |
dc.type.studyortrial | Clinical Trial | en_US |
dc.type.contenttype | Text | en_US |
Appears in Collections: | Cancer Services MOCI |
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