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低剂量口服依托泊苷治疗骨髓增生异常综合征患者。

Treatment with low-dose oral etoposide in patients with myelodysplastic syndromes.

作者信息

Doll D C, Kasper L M, Taetle R, List A F

机构信息

Department of Medicine, Harry S. Truman Memorial Veterans Hospital, University of Missouri, Columbia 65212, USA.

出版信息

Leuk Res. 1998 Jan;22(1):7-12. doi: 10.1016/s0145-2126(97)00149-5.

DOI:10.1016/s0145-2126(97)00149-5
PMID:9585073
Abstract

Forty-three patients with myelodysplastic syndromes (MDS) received treatment with oral etoposide 50 mg/day for 21 consecutive days every 4 weeks. Eighteen patients (42%) experienced hematological responses, including 12 of 17 (70%) patients with chronic myelomonocytic leukemia (CMML). Three of five CMML patients who failed treatment with hydroxyurea experienced major hematological responses with oral etoposide. Median response duration exceeded 9 months (range: 4-49 + months), and one patient remains in an unmaintained complete remission for 4 years. Toxicity included nausea/vomiting in five patients, fever (four patients), infection (three patients), mucositis (two patients), and anorexia (two patients). Two patients had grade 4 neutropenia with sepsis necessitating treatment withdrawal. We conclude that low-dose oral etoposide has remitting activity in MDS and is an effective treatment alternative for patients with CMML.

摘要

43例骨髓增生异常综合征(MDS)患者接受口服依托泊苷治疗,剂量为50mg/天,每4周连续用药21天。18例患者(42%)出现血液学反应,其中17例慢性粒单核细胞白血病(CMML)患者中有12例(70%)出现反应。5例接受羟基脲治疗失败的CMML患者中有3例口服依托泊苷后出现主要血液学反应。中位反应持续时间超过9个月(范围:4 - 49 +个月),1例患者持续未维持完全缓解达4年。毒性反应包括5例患者出现恶心/呕吐、4例发热、3例感染、2例黏膜炎和2例厌食。2例患者出现4级中性粒细胞减少伴败血症,需要停药。我们得出结论,低剂量口服依托泊苷对MDS有缓解活性,是CMML患者的一种有效治疗选择。

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The topoisomerase II inhibitor voreloxin causes cell cycle arrest and apoptosis in myeloid leukemia cells and acts in synergy with cytarabine.拓扑异构酶 II 抑制剂沃利替尼可引起髓系白血病细胞的细胞周期停滞和凋亡,并与阿糖胞苷协同作用。
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Pathogenesis, classification, and treatment of myelodysplastic syndromes (MDS).
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