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Early-onset Therapy-related Myelodysplastic Syndrome Originating from Prolonged Myelosuppression after Fludarabine-based Therapy
被引:4
作者:

Yamazaki, Sho
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h-index: 0
机构:
Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan

Nakamura, Fumihiko
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Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan

Nannya, Yasuhito
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h-index: 0
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Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan

Nakagawa, Masahiro
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Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan

Ichikawa, Motoshi
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h-index: 0
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Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan

Kurokawa, Mineo
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h-index: 0
机构:
Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan
Tokyo Univ Hosp, Dept Cell Therapy & Transplantat Med, Tokyo, Japan Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan
机构:
[1] Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo 1138654, Japan
[2] Tokyo Univ Hosp, Dept Cell Therapy & Transplantat Med, Tokyo, Japan
关键词:
chronic lymphocytic leukemia;
fludarabine-based therapy;
prolonged myelosuppression;
therapy-related myelodysplastic syndrome;
CHRONIC LYMPHOCYTIC-LEUKEMIA;
COMBINATION CHEMOTHERAPY;
CYCLOPHOSPHAMIDE;
D O I:
10.2169/internalmedicine.51.8310
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Fludarabine-based therapy is widely approved as a first-line treatment for chronic lymphocytic leukemia (CLL). This treatment is occasionally associated with prolonged myelosuppression. We herein describe the cases of CLL who underwent fludarabine, cyclophosphamide and rituximab (FCR) therapy. Bone marrow examinations performed during periods of prolonged myelosuppression revealed definite myelodysplastic changes in the myeloid and erythroid lineages. G-banded karyotyping analyses revealed cytogenetic abnormalities. The patients were diagnosed with therapy-related myelodysplastic syndrome (t-MDS). Further administration of cytotoxic therapy was aborted, and no progression of t-MDS was recorded throughout the follow-up period in either case. In these cases, the t-MDS was characterized by a short latency interval and a benign clinical course. Because typical t-MDS with aggressive outcomes also occurs during prolonged myelosuppression, the transition of the clinical course in this setting should therefore be carefully watched.
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页码:3427 / 3430
页数:4
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