Insights into treatment of patients with mycosis fungoides or Sézary syndrome using mogamulizumab

Purpose Mogamulizumab demonstrated improved outcomes vs. vorinostat across a range of disease and patient characteristics in patients with mycosis fungoides or Sézary syndrome in the MAVORIC trial.Materials and methods This post-hoc analysis further examined MAVORIC data to assess factors associated...

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Main Authors: Francine Foss, Youn H. Kim, Julia Scarisbrick, Oleg Akilov, Robert Ristuccia, Karen Dwyer, Wende Wu, Martine Bagot
Format: Article
Language:English
Published: Taylor & Francis Group 2025-12-01
Series:Journal of Dermatological Treatment
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Online Access:https://www.tandfonline.com/doi/10.1080/09546634.2024.2438794
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author Francine Foss
Youn H. Kim
Julia Scarisbrick
Oleg Akilov
Robert Ristuccia
Karen Dwyer
Wende Wu
Martine Bagot
author_facet Francine Foss
Youn H. Kim
Julia Scarisbrick
Oleg Akilov
Robert Ristuccia
Karen Dwyer
Wende Wu
Martine Bagot
author_sort Francine Foss
collection DOAJ
description Purpose Mogamulizumab demonstrated improved outcomes vs. vorinostat across a range of disease and patient characteristics in patients with mycosis fungoides or Sézary syndrome in the MAVORIC trial.Materials and methods This post-hoc analysis further examined MAVORIC data to assess factors associated with long-term response (ORR >12 months), time to next treatment (TTNT), and impact of concomitant steroid use, lymphopenia, and mogamulizumab-associated rash (MAR) on patient response.Results A higher proportion of patients achieved ORR lasting ≥4, 6, 8, or 12 months in the mogamulizumab vs. vorinostat arm. Long-term response was also observed in mogamulizumab-treated patients with more advanced disease (stage IVA1 [17/20], B2 blood involvement [18/20], and SS [14/20]). PFS was significantly longer (9.4 vs. 3.1 months; p < 0.0001) in mogamulizumab vs. vorinostat-treated patients taking concomitant steroids. Mogamulizumab-treated patients experienced longer TTNT vs. vorinostat. Lymphopenia and MAR were associated with response to mogamulizumab.Conclusions MAVORIC demonstrated greater efficacy with mogamulizumab vs. vorinostat in relapsed/refractory patients with CTCL, including those with more advanced disease. Concomitant steroid use improved ORR and PFS but did not impact vorinostat outcomes. Overall responses occurred more frequently in mogamulizumab-treated patients that developed lymphopenia than those that did not. A higher percentage of patients with MAR had an overall response than those without MAR.
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spelling doaj-art-eb78ed5180e54eb4908ac51a854068112025-02-03T01:01:43ZengTaylor & Francis GroupJournal of Dermatological Treatment0954-66341471-17532025-12-0136110.1080/09546634.2024.2438794Insights into treatment of patients with mycosis fungoides or Sézary syndrome using mogamulizumabFrancine Foss0Youn H. Kim1Julia Scarisbrick2Oleg Akilov3Robert Ristuccia4Karen Dwyer5Wende Wu6Martine Bagot7Yale Cancer Center, Yale University School of Medicine, New Haven, CT, USAStanford University, Stanford, CA, USAInstitute of Immunology and Immunotherapy, University Hospitals Birmingham, University of Birmingham, Birmingham, UKDepartment of Dermatology, University of Pittsburgh, Pittsburgh, PA, USAKyowa Kirin, Inc., Princeton, NJ, USAKyowa Kirin, Inc., Princeton, NJ, USAKyowa Kirin, Inc., Princeton, NJ, USAHôpital Saint Louis, APHP, Inserm U976, Université Paris Cité, Paris, FrancePurpose Mogamulizumab demonstrated improved outcomes vs. vorinostat across a range of disease and patient characteristics in patients with mycosis fungoides or Sézary syndrome in the MAVORIC trial.Materials and methods This post-hoc analysis further examined MAVORIC data to assess factors associated with long-term response (ORR >12 months), time to next treatment (TTNT), and impact of concomitant steroid use, lymphopenia, and mogamulizumab-associated rash (MAR) on patient response.Results A higher proportion of patients achieved ORR lasting ≥4, 6, 8, or 12 months in the mogamulizumab vs. vorinostat arm. Long-term response was also observed in mogamulizumab-treated patients with more advanced disease (stage IVA1 [17/20], B2 blood involvement [18/20], and SS [14/20]). PFS was significantly longer (9.4 vs. 3.1 months; p < 0.0001) in mogamulizumab vs. vorinostat-treated patients taking concomitant steroids. Mogamulizumab-treated patients experienced longer TTNT vs. vorinostat. Lymphopenia and MAR were associated with response to mogamulizumab.Conclusions MAVORIC demonstrated greater efficacy with mogamulizumab vs. vorinostat in relapsed/refractory patients with CTCL, including those with more advanced disease. Concomitant steroid use improved ORR and PFS but did not impact vorinostat outcomes. Overall responses occurred more frequently in mogamulizumab-treated patients that developed lymphopenia than those that did not. A higher percentage of patients with MAR had an overall response than those without MAR.https://www.tandfonline.com/doi/10.1080/09546634.2024.2438794Cutaneous T-cell lymphomamycosis fungoidesSézary syndromemogamulizumabC-C chemokine receptor 4
spellingShingle Francine Foss
Youn H. Kim
Julia Scarisbrick
Oleg Akilov
Robert Ristuccia
Karen Dwyer
Wende Wu
Martine Bagot
Insights into treatment of patients with mycosis fungoides or Sézary syndrome using mogamulizumab
Journal of Dermatological Treatment
Cutaneous T-cell lymphoma
mycosis fungoides
Sézary syndrome
mogamulizumab
C-C chemokine receptor 4
title Insights into treatment of patients with mycosis fungoides or Sézary syndrome using mogamulizumab
title_full Insights into treatment of patients with mycosis fungoides or Sézary syndrome using mogamulizumab
title_fullStr Insights into treatment of patients with mycosis fungoides or Sézary syndrome using mogamulizumab
title_full_unstemmed Insights into treatment of patients with mycosis fungoides or Sézary syndrome using mogamulizumab
title_short Insights into treatment of patients with mycosis fungoides or Sézary syndrome using mogamulizumab
title_sort insights into treatment of patients with mycosis fungoides or sezary syndrome using mogamulizumab
topic Cutaneous T-cell lymphoma
mycosis fungoides
Sézary syndrome
mogamulizumab
C-C chemokine receptor 4
url https://www.tandfonline.com/doi/10.1080/09546634.2024.2438794
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