Effects of tucidinostat in adult T-cell leukemia/lymphoma in clinical practice

Adult T-cell leukemia/lymphoma (ATL) is a peripheral T-cell malignancy with a poor prognosis. We conducted a retrospective study across six institutions in Miyazaki Prefecture, Japan, to assess the efficacy of tucidinostat in patients with relapsed/refractory ATL who had not undergone transplantation. Between October 2021 and July 2023, 24 patients aged 41 to 88 years (median, 73.4 years) who had undergone prior therapies, including intensive chemotherapy (79.2%) and mogamulizumab immunotherapy (79.2%), received tucidinostat. Objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), and overall survival (OS) were evaluated as key outcomes. ORR and DCR reached 54.2% and 91.7%, respectively. The median PFS was 3.95 months, and OS was 8.04 months, which were not inferior to the results of a phase IIb study. The influential factors for PFS were age ≥ 75 years and high soluble IL-2 receptor (sIL-2R) levels above 5000 U/mL at the start of treatment. Favorable patients without these factors achieved a PFS of 11.4 months. Treatment-related adverse events were mainly hematologic but were managed over the course of treatment. Our findings indicate that tucidinostat provides survival benefits in patients with relapsed/refractory ATL in clinical practice and highlight key clinical factors for better outcomes.

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Publication Details

Journal
International Journal of Hematology
Published
2025-03-11
DOI
https://doi.org/10.1007/s12185-025-03963-9
Citations
2
Primary Topic
T-cell and Retrovirus Studies
Type
article
Field-Weighted Citation Impact
1.59

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article

Effects of tucidinostat in adult T-cell leukemia/lymphoma in clinical practice

Keiichi Akizuki, Ayako Kamiunten, Taisuke Uchida, Kengo Matsumoto et al.
2 citations
International Journal of Hematology
T-cell and Retrovirus Studies
1.59
article

Effects of tucidinostat in adult T-cell leukemia/lymphoma in clinical practice

Keiichi Akizuki, Ayako Kamiunten, Taisuke Uchida, Kengo Matsumoto, Takuro Kameda, Yoko Kubuki, Aki Kuroki, Tomonori Hidaka, Kotaro Shide, Kentaro Nagamine, Haruko Shimoda, Kiyoshi Yamashita, Masayoshi Karasawa, Junzo Ishizaki, Yuki Tahira, Masaaki Sekine, Seiichi Sato, Kazuya Shimoda, Kouichi Maeda, Hiroshi Kawano, Hideki Yamaguchi, Masanori Takeuchi, Takanori Toyama, Ryoma Ikeda, Noriaki Kawano
article en
2 citations

Abstract

Adult T-cell leukemia/lymphoma (ATL) is a peripheral T-cell malignancy with a poor prognosis. We conducted a retrospective study across six institutions in Miyazaki Prefecture, Japan, to assess the efficacy of tucidinostat in patients with relapsed/refractory ATL who had not undergone transplantation. Between October 2021 and July 2023, 24 patients aged 41 to 88 years (median, 73.4 years) who had undergone prior therapies, including intensive chemotherapy (79.2%) and mogamulizumab immunotherapy (79.2%), received tucidinostat. Objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), and overall survival (OS) were evaluated as key outcomes. ORR and DCR reached 54.2% and 91.7%, respectively. The median PFS was 3.95 months, and OS was 8.04 months, which were not inferior to the results of a phase IIb study. The influential factors for PFS were age ≥ 75 years and high soluble IL-2 receptor (sIL-2R) levels above 5000 U/mL at the start of treatment. Favorable patients without these factors achieved a PFS of 11.4 months. Treatment-related adverse events were mainly hematologic but were managed over the course of treatment. Our findings indicate that tucidinostat provides survival benefits in patients with relapsed/refractory ATL in clinical practice and highlight key clinical factors for better outcomes.

International Journal of HematologyVol. 122(1)
University of Miyazaki (JP), Miyazaki Prefectural Hospital (JP), Koga Hospital (JP), National Institute of Technology, Miyakonojo College (JP)
University of Miyazaki Hospital, University of Miyazaki
Good health and well-being
Openalex Percentile: Top 19%
T-cell and Retrovirus Studies
1.59
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