Long-term study of indolent adult T-cell leukemia-lymphoma

Author:

Takasaki Yumi12,Iwanaga Masako23,Imaizumi Yoshitaka2,Tawara Masayuki12,Joh Tatsuro12,Kohno Tomoko4,Yamada Yasuaki5,Kamihira Shimeru5,Ikeda Schuichi6,Miyazaki Yasushi2,Tomonaga Masao1,Tsukasaki Kunihiro2

Affiliation:

1. Third Department of Internal Medicine, Japanese Red Cross Nagasaki Genbaku Hospital, Nagasaki;

2. Department of Molecular Medicine and Hematology, Molecular Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki;

3. Department of Nutritional Health, Faculty of Wellness Studies, Kwassui Women's College, Nagasaki;

4. Division of Cytokine Signaling, Department of Molecular Microbiology and Immunology and

5. Department of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki; and

6. Department of Hematology, Hirado Municipal Hospital, Nagasaki, Japan

Abstract

Abstract The long-term prognosis of indolent adult T-cell leukemia-lymphoma (ATL) is not clearly elucidated. From 1974 to 2003, newly diagnosed indolent ATL in 90 patients (65 chronic type and 25 smoldering type) was analyzed. The median survival time was 4.1 years; 12 patients remained alive for more than 10 years, 44 progressed to acute ATL, and 63 patients died. The estimated 5-, 10-, and 15-year survival rates were 47.2%, 25.4%, and 14.1%, respectively, with no plateau in the survival curve. Although most patients were treated with watchful waiting, 12 patients were treated with chemotherapy. Kaplan-Meier analyses showed that advanced performance status (PS), neutrophilia, high concentration of lactate dehydrogenase, more than 3 extranodal lesions, more than 4 total involved lesions, and receiving chemotherapy were unfavorable prognostic factors for survival. Multivariate Cox analysis showed that advanced PS was a borderline significant independent factor in poor survival (hazard ratio, 2.1, 95% confidence interval, 1.0-4.6; P = .06), but it was not a factor when analysis was limited to patients who had not received chemotherapy. The prognosis of indolent ATL in this study was poorer than expected. These findings suggest that even patients with indolent ATL should be carefully observed in clinical practice. Further studies are required to develop treatments for indolent ATL.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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