Maintenance therapy with romidepsin after autologous stem-cell transplant for peripheral T-cell lymphoma

Patients with peripheral T-cell lymphoma (PTCL) have suboptimal outcomes. Autologous hematopoietic stem-cell transplantation (AHCT) is a therapeutic strategy for patients in first complete remission (CR1) or first partial remission (PR1), with median intent-to-treat progression-free survival (PFS) of 36% to 48%. Romidepsin is a histone deacetylase inhibitor used for treatment of relapsed/refractory PTCL. We present a multicenter study to evaluate the PFS of patients receiving maintenance therapy with romidepsin after AHCT. Twenty-six patients who underwent AHCT in CR1 or PR1 were evaluated for the primary end point of 2-year PFS. The exploratory cohort enrolled patients who underwent transplantation during or after CR/PR2 (n = 5) or high-risk histologies (n = 2). Patients underwent AHCT with carmustine, etoposide, cytarabine, and melphalan conditioning. Romidepsin 14 mg/m2 was started on days 42 to 80 after -AHCT every other week until 6 months of -AHCT, every 3 weeks between 6 months and 1-year of -AHCT, and every 4 weeks between 1 and 2 years of -AHCT. PFS was estimated using the Kaplan-Meier analysis. Forty-seven patients consented and 13 did not receive romidepsin. With a median progression-free follow-up of 32 months (range, 24-36), 15 of the first 25 patients in cohort 1 were progression-free after 2 years. The estimated 2-year PFS was 62% (95% confidence interval, 45-83). The most common toxicities were fatigue (n = 24, 73%), decreased platelets (n = 16, 48%), and anemia (n = 16, 48%). Although the study did not meet its desired primary efficacy end point, maintenance romidepsin was feasible, with a favorable estimated 2-year PFS of 62%. This trial was registered at www.ClinicalTrials.gov as #NCT01908777.

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Journal
Blood Advances
Published
2025-04-04
DOI
https://doi.org/10.1182/bloodadvances.2024014263
Citations
1
Primary Topic
T-cell and Retrovirus Studies
Type
article
Field-Weighted Citation Impact
0.80

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article

Maintenance therapy with romidepsin after autologous stem-cell transplant for peripheral T-cell lymphoma

David J. Straus, Ariela Noy, Farhad Khimani, Gunjan L. Shah et al.
1 citations
Blood Advances
T-cell and Retrovirus Studies
0.80
article

Maintenance therapy with romidepsin after autologous stem-cell transplant for peripheral T-cell lymphoma

David J. Straus, Ariela Noy, Farhad Khimani, Gunjan L. Shah, Helen Hancock, Craig S. Sauter, Koen van Besien, Parastoo Bahrami Dahi, Esther N Drill, Matthew J. Matasar, Mazyar Shadman, Jia Ruan, Pamela R. Drullinsky, Andrei R. Shustov, Andrew David Zelenetz, Alison J. Moskowitz, Natasha Galasso, Sergio A. Giralt, Theresa Davey, Niloufer Khan, Anita Kumar, Sarah McCue Horwitz, Nivetha Ganesan, Audrey M. Hamilton
article en
1 citations

Abstract

Patients with peripheral T-cell lymphoma (PTCL) have suboptimal outcomes. Autologous hematopoietic stem-cell transplantation (AHCT) is a therapeutic strategy for patients in first complete remission (CR1) or first partial remission (PR1), with median intent-to-treat progression-free survival (PFS) of 36% to 48%. Romidepsin is a histone deacetylase inhibitor used for treatment of relapsed/refractory PTCL. We present a multicenter study to evaluate the PFS of patients receiving maintenance therapy with romidepsin after AHCT. Twenty-six patients who underwent AHCT in CR1 or PR1 were evaluated for the primary end point of 2-year PFS. The exploratory cohort enrolled patients who underwent transplantation during or after CR/PR2 (n = 5) or high-risk histologies (n = 2). Patients underwent AHCT with carmustine, etoposide, cytarabine, and melphalan conditioning. Romidepsin 14 mg/m2 was started on days 42 to 80 after -AHCT every other week until 6 months of -AHCT, every 3 weeks between 6 months and 1-year of -AHCT, and every 4 weeks between 1 and 2 years of -AHCT. PFS was estimated using the Kaplan-Meier analysis. Forty-seven patients consented and 13 did not receive romidepsin. With a median progression-free follow-up of 32 months (range, 24-36), 15 of the first 25 patients in cohort 1 were progression-free after 2 years. The estimated 2-year PFS was 62% (95% confidence interval, 45-83). The most common toxicities were fatigue (n = 24, 73%), decreased platelets (n = 16, 48%), and anemia (n = 16, 48%). Although the study did not meet its desired primary efficacy end point, maintenance romidepsin was feasible, with a favorable estimated 2-year PFS of 62%. This trial was registered at www.ClinicalTrials.gov as #NCT01908777.

Blood AdvancesVol. 9(18)
City Of Hope National Medical Center (US), Memorial Sloan Kettering Cancer Center (US), University of Washington (US), Cornell University (US), Moffitt Cancer Center (US), City of Hope (US)
AstraZeneca, Gilead Sciences, Celgene, TG Therapeutics, BeiGene, Incyte, MorphoSys, National Institutes of Health, Genentech, Pharmacyclics
Good health and well-being
Openalex Percentile: Top 30%
T-cell and Retrovirus Studies
0.80
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