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Clinical factors to predict outcome following mogamulizumab in adult T-cell leukemia-lymphoma
被引:0
|作者:
Jun Nakashima
Yoshitaka Imaizumi
Hiroaki Taniguchi
Koji Ando
Masako Iwanaga
Hidehiro Itonaga
Shinya Sato
Yasuhi Sawayama
Tomoko Hata
Shinichiro Yoshida
Yukiyoshi Moriuchi
Yasushi Miyazaki
机构:
[1] Nagasaki University Graduate School of Biomedical Sciences,Atomic Bomb Disease and Hibakusha Medicine Unit, Department of Hematology
[2] National Hospital Organization Nagasaki Medical Center,Department of Hematology
[3] Nagasaki University Hospital,Department of Hematology
[4] Sasebo City General Medical Center,Department of Hematology
[5] Nagasaki University Graduate School of Biomedical Science,Department of Frontier Life Science
来源:
International Journal of Hematology
|
2018年
/
108卷
关键词:
ATL;
Mogamulizumab;
Prognostic factors;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
Adult T-cell leukemia–lymphoma (ATL) is a distinct T-cell malignancy caused by human T-cell leukemia virus type-1; the prognosis is very poor. Mogamulizumab (Moga), an antibody drug for CC chemokine receptor type 4, has been introduced for the treatment of ATL. However, the prognosis of relapsed or refractory ATL remains poor and the characteristics of patients who derive clinical benefit from treatment with Moga remain poorly understood. We analyzed the associations of clinical factors with the outcome after Moga treatment. Forty-five patients treated with Moga monotherapy were evaluated. The median age of the patients was 69 years, and 40% were female. The median overall survival (OS) time was 17.6 months and the 2-year OS rate was 43.2%. Number of prior therapies and response to prior therapy were predictive clinical features in univariate analysis for OS. Performance status, corrected serum calcium level, serum lactate dehydrogenase level, Japan Clinical Oncology Group-prognostic index (PI), and simplified ATL-PI at Moga treatment were also associated with the prognosis after Moga monotherapy. Improved understanding of the clinical factors predicting the prognosis after Moga may contribute to improved treatment strategies for ATL.
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页码:516 / 523
页数:7
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