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. 2024 Dec;120(6):694-704.
doi: 10.1007/s12185-024-03857-2. Epub 2024 Oct 10.

Improved survival among elderly patients with aggressive adult T-cell leukemia/lymphoma: Impact of mogamulizumab-containing chemotherapy

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Improved survival among elderly patients with aggressive adult T-cell leukemia/lymphoma: Impact of mogamulizumab-containing chemotherapy

Miki Hashimoto et al. Int J Hematol. 2024 Dec.

Abstract

Due to the poor prognosis of adult T-cell leukemia/lymphoma (ATL), new treatments are urgently needed, especially for elderly patients with aggressive ATL. The anti-CCR4 antibody drug mogamulizumab (MOG) has been approved for the treatment of untreated ATL. To analyze the impact of MOG on elderly patients, we conducted a retrospective analysis of patients aged 70 years and older with aggressive ATL diagnosed at our institution between 2015 and 2021. Among 32 patients, including those who received best supportive care, the median survival time (MST) and 2-year overall survival (OS) rate were 14.6 months (range, 0.0-83.7), and 34.7% [95% confidence interval (CI), 18.2-51.9], respectively, which were better than outcomes in our previous study. The MST and 2-year OS for patients treated with MOG-containing chemotherapy were 18.1 months (range, 4.0-83.7) and 45.0% (95%CI, 23.1-64.7), respectively, demonstrating clear improvement. Adverse events observed with MOG-containing treatment, such as myelosuppression and skin rash, were similar to those reported previously. Univariate analysis identified comorbidity as a predictor of poor outcomes, but not intensity of MOG-containing treatment, suggesting a different mechanism of action than that of classical chemotherapy. Our study suggests that MOG-containing treatments are an option for elderly patients with ATL.

Keywords: ATL; Chemotherapy; Elderly; Mogamulizumab.

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Conflict of interest statement

Declarations. Conflict of interest: Yasushi Miyazaki is an associate editor of International Journal of Hematology. Yasushi Miyazaki has received honoraria from Astellas Pharma, Chugai, Kyowa Kirin, Nippon Shinyaku, Novartis, Abbvie, Bristol-Myers Squibb, Sumitomo Pharma, SymBio, Daiichi Sankyo, and has received research funding from Chugai. Y. Imaizumi has received honoraria from Chugai, Sanofi, Daiichi Sankyo, SymBio, Meiji Seika Pharma, Astra Zeneca, Bristol-Myers Squibb, Kyowa Kirin. All the remaining authors declare no conflict of interest.

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