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首页> 外文期刊>Haematologica >Phase II trial of vorinostat and gemtuzumab ozogamicin as induction and post-remission therapy in older adults with previously untreated acute myeloid leukemia | Haematologica
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Phase II trial of vorinostat and gemtuzumab ozogamicin as induction and post-remission therapy in older adults with previously untreated acute myeloid leukemia | Haematologica

机译:伏立诺他和吉妥珠单抗奥佐米星在先前未经治疗的急性髓性白血病的老年人中的诱导和缓解后治疗的II期试验|血液学

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Histone deacetylase inhibitors such as vorinostat enhance gemtuzumab ozogamicin efficacy in vitro. We, therefore, investigated vorinostat+gemtuzumab ozogamicin for adults aged 60 years and over with untreated acute myeloid leukemia. We stratified patients into 2 groups (group 1: patients aged ≥70 years and performance status 2–3; group 2: aged 60–69 years with performance status 0–3 or aged ≥70 years and performance status 0–1). Responses were monitored separately in group 2 patients with normal or favorable cytogenetics (group 2A) and other cytogenetics (group 2B). Among 31 patients, 6 (19.4%) achieved complete remission, and one (3.2%) achieved complete remission with incomplete platelet recovery; these patients had a higher median overall survival than non-responders (553 vs. 131 days, P=0.0026). Response rates were: group 1, one of 10 (10.0%); group 2A, 6 of 13 (46.2%); and group 2B, none of 8 (0%). These data indicate that vorinostat+gemtuzumab ozogamicin has activity that is mostly confined to patients with normal karyotype disease. ClinicalTrial.gov: NCT00673153.
机译:组蛋白脱乙酰基酶抑制剂(例如伏立诺他)在体外增强吉妥单抗ozogamicin的功效。因此,我们对未治疗的急性髓细胞性白血病的60岁及以上成年人进行了伏立诺他+吉妥单抗ozogamicin的研究。我们将患者分为两组(第1组:年龄≥70岁且机能状态为2-3的患者;第2组:60-69岁的患者,机能状态为0-3或≥70岁的患者,机能状态为0-1)。分别对第2组细胞遗传学正常或良好(第2A组)和其他细胞遗传学(第2B组)的患者进行反应监测。在31例患者中,有6例(19.4%)实现了完全缓解,其中1例(3.2%)实现了完全缓解,血小板恢复不完全。这些患者的中位总体生存率高于无反应者(553天与131天,P = 0.0026)。回应率是:第一组,10个中的一个(10.0%);第2A组,共13个中的6个(46.2%);和2B组,全无8(0%)。这些数据表明伏立诺他+吉妥单抗ozogamicin的活性主要局限于正常核型患者。 ClinicalTrial.gov:NCT00673153。

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