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Nationwide survey on the use of eltrombopag in patients with severe aplastic anemia: a report on behalf of the French Reference Center for Aplastic Anemia

机译:全国关于严重再生障碍性贫血患者使用Eltrombopag的调查:代表法国再生障碍性贫血参考中心的一份报告

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Few therapeutic options are available for patients with aplastic anemia who are ineligible for transplantation or refractory to immunosuppressive therapy. Eltrombopag was recently shown to produce trilineage responses in refractory patients. However, the effects of real-life use of this drug remain unknown. This retrospective study (2012–2016) was conducted by the French Reference Center for Aplastic Anemia on patients with relapsed/refractory aplastic anemia, and patients ineligible for antithymocyte globulin or transplantation, who received eltrombopag for at least 2 months. Forty-six patients with aplastic anemia were given eltrombopag without prior antithymocyte globulin treatment (n=11) or after antithymocyte globulin administration (n=35) in a relapsed/refractory setting. Eltrombopag (median daily dose 150 mg) was introduced 17 months (range, 8–50) after the diagnosis of aplastic anemia. At last followup, 49% were still receiving treatment, 9% had stopped due to a robust response, 2% due to toxicity and 40% due to eltrombopag failure. Before eltrombopag treatment, all patients received regular transfusions. The overall rates of red blood cell and platelet transfusion independence were 7%, 33%, 46% and 46% at 1, 3, 6 months and last follow-up. Responses were slower to develop in antithymocyte treatment-na?ve patients. In patients achieving transfusion independence, hemoglobin concentration and platelet counts improved by 3 g/dL (interquartile range, 1.4–4.5) and 42×10~(9)/L (interquartile range, 11–100), respectively. Response in at least one lineage (according to National Institutes of Health criteria) was observed in 64% of antithymocyte treatment-na?ve and 74% of relapsed/refractory patients, while trilineage improvement was observed in 27% and 34%, respectively. We found high rates of hematologic improvement and transfusion independence in refractory aplastic anemia patients but also in patients ineligible for antithymocyte globulin receiving first-line treatment. In conclusion, elderly patients unfit for antithymocyte globulin therapy may benefit from eltrombopag.
机译:对于再生障碍性贫血不适合移植或免疫抑制治疗无效的患者,几乎没有治疗选择。最近显示Eltrombopag在难治性患者中产生三联反应。但是,该药物在现实生活中的使用效果仍然未知。这项回顾性研究(2012-2016年)是由法国再生障碍性贫血参考中心对复发/难治性再生障碍性贫血以及没有资格接受抗胸腺细胞球蛋白或移植治疗且接受Eltrombopag至少2个月的患者进行的。 46例再生障碍性贫血患者在复发/难治性环境中接受了未经预先给予抗胸腺细胞球蛋白治疗(n = 11)或给予抗胸腺细胞球蛋白治疗(n = 35)后的Eltrombopag。在诊断再生障碍性贫血后17个月(范围8–50)引入Eltrombopag(每日平均剂量150 mg)。在最后一次随访中,仍有49%的患者仍在接受治疗,有9%的患者因反应强烈而停止治疗,有2%的患者因毒性反应而40%的患者因Eltrombopag衰竭而停药。在接受Eltrombopag治疗之前,所有患者均接受定期输血。在1、3、6个月和最后一次随访时,红细胞和血小板输注独立性的总发生率分别为7%,33%,46%和46%。初次接受抗胸腺细胞治疗的患者反应较慢。在达到输血独立性的患者中,血红蛋白浓度和血小板计数分别提高了3 g / dL(四分位间距为1.4-4.5)和42×10〜(9)/ L(四分位间距为11-100)。至少有64%的初次接受抗胸腺细胞治疗的患者和74%的复发/难治性患者观察到了至少一种谱系的反应(根据美国国立卫生研究院的标准),而三谱系的改善分别达到了27%和34%。我们发现难治性再生障碍性贫血患者以及不适合接受一线治疗的抗胸腺细胞球蛋白的患者血液学改善和输血独立性较高。总之,不适合抗胸腺细胞球蛋白治疗的老年患者可从厄洛托巴糖中获益。

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