Mogamulizumab in combination improves clinical outcomes in relapsed and refractory Sézary syndrome

Introduction Sézary syndrome (SS) is an aggressive variant of cutaneous T-cell lymphoma (CTCL) that presents with generalized erythroderma, lymphadenopathy, peripheral blood involvement, and severe pruritus. Unfortunately, the disease can relapse or progress and generally has a poor prognosis. Mogamulizumab is a targeted monoclonal antibody that has been shown to be effective in relapsed disease, with particular benefit in the blood compartment, and has received the U.S. Food and Drug Administration (FDA) approval for CTCL. Data regarding the combination of mogamulizumab with other systemic treatments for CTCL are limited. Here, we present clinical outcomes in a real-world setting where patients with SS were treated using a mogamulizumab-based multi-agent approach. Methods and results We conducted a retrospective chart review of patients in a Cutaneous Lymphoma Clinic and identified 10 patients that met the International Society for Cutaneous Lymphomas (ISCL)/European Organization of Research and Treatment of Cancer (EORTC) diagnostic criteria for SS and were treated with mogamulizumab. These patients received at least four prior therapies, including systemics and topicals. All patients received mogamulizumab in addition to other systemic therapies. Responses were commonly observed in the blood after the first cycle. Global response, determined by assessment in four compartments including the skin, blood, viscera, and lymph nodes, identified four patients that achieved complete remission, three with partial response, two that maintained a stable disease, and one patient that experienced disease progression. The therapies most frequently used in combination were bexarotene and interferon. The median duration of response in our patient population was 23.5 months. Conclusion In this case series, a multi-agent approach combining mogamulizumab with traditional CTCL systemic agents was well tolerated and was effective in the treatment of relapsed or refractory SS and led to a period of extended clinical improvement.

Authors

Institutions

Publication Details

Journal
Frontiers in Hematology
Published
2025-05-14
DOI
https://doi.org/10.3389/frhem.2025.1557641
Primary Topic
Cutaneous lymphoproliferative disorders research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Mogamulizumab in combination improves clinical outcomes in relapsed and refractory Sézary syndrome

Jordan Pilkington, Delice Kayishunge, Cesar Gentille, Henry K. Wong et al.
Frontiers in Hematology
Cutaneous lymphoproliferative disorders research
article

Mogamulizumab in combination improves clinical outcomes in relapsed and refractory Sézary syndrome

Jordan Pilkington, Delice Kayishunge, Cesar Gentille, Henry K. Wong, Sophia Ly
article en

Abstract

Introduction Sézary syndrome (SS) is an aggressive variant of cutaneous T-cell lymphoma (CTCL) that presents with generalized erythroderma, lymphadenopathy, peripheral blood involvement, and severe pruritus. Unfortunately, the disease can relapse or progress and generally has a poor prognosis. Mogamulizumab is a targeted monoclonal antibody that has been shown to be effective in relapsed disease, with particular benefit in the blood compartment, and has received the U.S. Food and Drug Administration (FDA) approval for CTCL. Data regarding the combination of mogamulizumab with other systemic treatments for CTCL are limited. Here, we present clinical outcomes in a real-world setting where patients with SS were treated using a mogamulizumab-based multi-agent approach. Methods and results We conducted a retrospective chart review of patients in a Cutaneous Lymphoma Clinic and identified 10 patients that met the International Society for Cutaneous Lymphomas (ISCL)/European Organization of Research and Treatment of Cancer (EORTC) diagnostic criteria for SS and were treated with mogamulizumab. These patients received at least four prior therapies, including systemics and topicals. All patients received mogamulizumab in addition to other systemic therapies. Responses were commonly observed in the blood after the first cycle. Global response, determined by assessment in four compartments including the skin, blood, viscera, and lymph nodes, identified four patients that achieved complete remission, three with partial response, two that maintained a stable disease, and one patient that experienced disease progression. The therapies most frequently used in combination were bexarotene and interferon. The median duration of response in our patient population was 23.5 months. Conclusion In this case series, a multi-agent approach combining mogamulizumab with traditional CTCL systemic agents was well tolerated and was effective in the treatment of relapsed or refractory SS and led to a period of extended clinical improvement.

Frontiers in HematologyVol. 4
Winthrop Rockefeller Foundation (US), University of Arkansas for Medical Sciences (US)
Openalex Percentile: Top 80%
Cutaneous lymphoproliferative disorders research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.