Romidepsin and mogamulizumab sequential treatment for advanced cutaneous T-cell lymphoma

Management of advanced stage cutaneous T-cell lymphoma (CTCL) can be challenging due to lack of durable responses to currently available therapies and their side effects and toxicities. Romidepsin, a histone deacetylase inhibitor, and mogamulizumab, an anti-CCR4 monoclonal antibody, have demonstrated some efficacy as monotherapies, however, survival outcomes remain poor. This retrospective study evaluates the effectiveness of sequential romidepsin-mogamulizumab (Romi-Moga) therapy in 18 patients with advanced CTCL. The overall response rate was 67% in our cohort and time to next treatment was 15 months, which compared favorably to clinical trials of monotherapies. Patients who transitioned to mogamulizumab within one month of romidepsin discontinuation exhibited superior responses in skin, blood, and lymph nodes and longer time to next treatment. These findings suggest a potential beneficial effect of Romi-Moga therapy when administered in close sequence. Prospective studies are needed to validate these results and optimize treatment strategies.

Authors

Institutions

Publication Details

Journal
Leukemia & lymphoma/Leukemia and lymphoma
Published
2025-08-11
DOI
https://doi.org/10.1080/10428194.2025.2542941
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

Romidepsin and mogamulizumab sequential treatment for advanced cutaneous T-cell lymphoma

Larisa J. Geskin, Barbara Pro, Susan E. Bates, Oluwaseyi Adeuyan et al.
Leukemia & lymphoma/Leukemia and lymphoma
Cutaneous lymphoproliferative disorders research
article

Romidepsin and mogamulizumab sequential treatment for advanced cutaneous T-cell lymphoma

Larisa J. Geskin, Barbara Pro, Susan E. Bates, Oluwaseyi Adeuyan, Brigit A. Lapolla, Manuel A. Pazos, Ted B. Piorczynski, Megan H. Trager, David M. DeStephano, Emily R. Gordon, Seda S. Tolu, Jennifer E. Amengual
article en

Abstract

Management of advanced stage cutaneous T-cell lymphoma (CTCL) can be challenging due to lack of durable responses to currently available therapies and their side effects and toxicities. Romidepsin, a histone deacetylase inhibitor, and mogamulizumab, an anti-CCR4 monoclonal antibody, have demonstrated some efficacy as monotherapies, however, survival outcomes remain poor. This retrospective study evaluates the effectiveness of sequential romidepsin-mogamulizumab (Romi-Moga) therapy in 18 patients with advanced CTCL. The overall response rate was 67% in our cohort and time to next treatment was 15 months, which compared favorably to clinical trials of monotherapies. Patients who transitioned to mogamulizumab within one month of romidepsin discontinuation exhibited superior responses in skin, blood, and lymph nodes and longer time to next treatment. These findings suggest a potential beneficial effect of Romi-Moga therapy when administered in close sequence. Prospective studies are needed to validate these results and optimize treatment strategies.

Leukemia & lymphoma/Leukemia and lymphomaVol. 66(12)
Columbia University Irving Medical Center (US), Columbia College (CA), Royal College of Physicians (GB), Columbia University (US)
Openalex Percentile: Top 64%
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.

Romidepsin and mogamulizumab sequential treatment for advanced cutaneous T-cell lymphoma — Larisa J. Geskin, Barbara Pro, et al. · Leukemia & lymphoma/Leukemia and lymphoma (2025) | TGRS Research Map | TGRS