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Title: | Lack of durable remission with conventional-dose total skin electron therapy for the management of Sezary syndrome and multiple relapsed mycosis fungoides. |
Epworth Authors: | Prince, Miles |
Other Authors: | Campbell, Belinda Ryan, Gail McCormack, Christopher Tangas, Eleanor Bressel, Mathias Twigger, Robert Buelens, Odette van der Weyden, Carrie |
Keywords: | Durable Remission Conventional-Dose Total Skin Electron Therapy (TSE) Sezary Syndrome Multiply Relapsed Mycosis Fungoides (MF) Cutaneous T-cell Lymphomas Conventional-dose TSE (cdTSE) Symptom Control Tolerability Against Response Durability Overall Survival (OS) Inferior Prognosis Skin-Directed Therapy Time to Next Treatment (TTNT) Systemic Treatments Haematopoietic Stem Cell Transplantation (HSCT) High-Grade Transformation Autologous Stem Cell Transplant (SCT) Allogeneic Haematopoietic SCT (HSCT) Chemotherapy Rotary-Dual Technique Surrogate endpoint Epworth Centre for Immunotherapies and Snowdome Laboratories Molecular Oncology and Cancer Immunology Cancer Services Clinical Institute, Epworth HealthCare, Victoria, Australia |
Issue Date: | Nov-2019 |
Publisher: | Multidisciplinary Digital Publishing Institute (MDPI) |
Citation: | Cancers, 11(11), 1758. |
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. |
URI: | http://hdl.handle.net/11434/2043 |
DOI: | 10.3390/cancers11111758 |
PubMed URL: | https://pubmed.ncbi.nlm.nih.gov/31717353 |
ISSN: | 2072-6694 |
Journal Title: | Cancers (Basel) |
Type: | Journal Article |
Affiliated Organisations: | Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne 3000, Victoria, Australia Department of Clinical Pathology, The University of Melbourne, Parkville 3010, Victoria, Australia Department of Surgical Oncology, Peter MacCallum Cancer Centre, Melbourne 3000, Victoria, Australia Department of Dermatology, St Vincent’s Hospital Melbourne, Fitzroy 3065, Victoria, Australia Melbourne Clinical School, School of Medicine, University of Notre Dame, Werribee 3030, Victoria, Australia Centre for Biostatics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne 3000, Victor Department of Clinical Haematology, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne 3000, Victoria, Australia Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville 3010, Victoria, Australia |
Type of Clinical Study or Trial: | Clinical Trial |
Appears in Collections: | Cancer Services MOCI |
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