首页> 外文期刊>International journal of hematology >Long-term pattern of pleural effusion from chronic myeloid leukemia patients in second-line dasatinib therapy.
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Long-term pattern of pleural effusion from chronic myeloid leukemia patients in second-line dasatinib therapy.

机译:达沙替尼二线治疗对慢性粒细胞白血病患者的长期胸腔积液。

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Dasatinib is a potent second-generation tyrosine kinase inhibitor approved for the treatment of chronic myeloid leukemia after imatinib failure. However, some patients treated with dasatinib experience pleural effusions (PEs). The determinants of pleural effusion in long-term dasatinib treatment (median 35 months, range 1-55) were investigated in single-center data of 65 patients enrolled in global phase 2 and phase 3 trials. Of the 65 patients, 35 (54%) developed dasatinib-induced pleural effusion (a median onset time, 20 months; range 0.2-54). The first pleural effusion developed in 15 (43%) patients within 12 months of dasatinib therapy. Disease phase (P = 0.02), dose schedule (P = 0.002) and actual daily mean dose (P = 0.0002) were significantly associated with an increased risk of pleural effusion. Twice-daily administration of dasatinib resulted in significantly more patients developing pleural effusions compared with the once-daily dosing schedule, particularly in advanced disease. In addition, a strong correlation was found between actual daily mean dose and time to onset of pleural effusions in patients treated with a daily mean dose >100 mg/day of dasatinib (P = 0.01). These data emphasize the need for dasatinib dose and schedule optimization and long-term monitoring of dasatinib-treated patients to prevent the negative clinical implications of pleural effusion.
机译:达沙替尼是一种有效的第二代酪氨酸激酶抑制剂,已批准用于伊马替尼治疗失败后的慢性粒细胞白血病。但是,某些接受达沙替尼治疗的患者会出现胸腔积液(PEs)。在全球2期和3期试验的65名患者的单中心数据中,调查了长期达沙替尼治疗(中位数35个月,范围1-55)中胸腔积液的决定因素。在65例患者中,有35例(54%)发生了达沙替尼诱导的胸腔积液(中位发作时间为20个月;范围为0.2-54)。在达沙替尼治疗后的12个月内,有15位(43%)患者发生了首次胸腔积液。疾病阶段(P = 0.02),给药方案(P = 0.002)和实际每日平均剂量(P = 0.0002)与胸腔积液风险增加显着相关。与每日一次的给药方案相比,达沙替尼的每日两次给药导致出现胸腔积液的患者明显增多,尤其是在晚期疾病中。此外,在每日平均剂量大于100毫克/天的达沙替尼治疗的患者中,实际每日平均剂量与发生胸腔积液的时间之间存在很强的相关性(P = 0.01)。这些数据强调需要达沙替尼剂量和时间表的优化以及对达沙替尼治疗的患者的长期监测,以防止胸腔积液的不良临床影响。

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