Emily R Gordon, Seda Tolu, Brigit A Lapolla, Megan H Trager, Oluwaseyi Adeuyan, Manuel A Pazos, Ted Piorczynski, David DeStephano, Susan E Bates, Barbara Pro, Jennifer E Amengual, Larisa J Geskin
{"title":"罗米地辛和莫加单抗序贯治疗晚期皮肤t细胞淋巴瘤。","authors":"Emily R Gordon, Seda Tolu, Brigit A Lapolla, Megan H Trager, Oluwaseyi Adeuyan, Manuel A Pazos, Ted Piorczynski, David DeStephano, Susan E Bates, Barbara Pro, Jennifer E Amengual, Larisa J Geskin","doi":"10.1080/10428194.2025.2542941","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":18047,"journal":{"name":"Leukemia & Lymphoma","volume":" ","pages":"1-8"},"PeriodicalIF":2.2000,"publicationDate":"2025-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Romidepsin and mogamulizumab sequential treatment for advanced cutaneous T-cell lymphoma.\",\"authors\":\"Emily R Gordon, Seda Tolu, Brigit A Lapolla, Megan H Trager, Oluwaseyi Adeuyan, Manuel A Pazos, Ted Piorczynski, David DeStephano, Susan E Bates, Barbara Pro, Jennifer E Amengual, Larisa J Geskin\",\"doi\":\"10.1080/10428194.2025.2542941\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":18047,\"journal\":{\"name\":\"Leukemia & Lymphoma\",\"volume\":\" \",\"pages\":\"1-8\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-08-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Leukemia & Lymphoma\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/10428194.2025.2542941\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Leukemia & Lymphoma","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/10428194.2025.2542941","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"HEMATOLOGY","Score":null,"Total":0}
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.
期刊介绍:
Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor