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Autologous transplantation gives encouraging results for young adults with favorable-risk acute myeloid leukemia, but is not improved with gemtuzumab ozogamicin

机译:自体移植为年轻人带来了有利风险的急性髓性白血病,但令人欣喜的结果,但吉妥单抗ozogamicin并不能改善

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摘要

We report the results of a prospective, randomized phase 3 trial evaluating the use of gemtuzumab ozogamicin (GO) in an intensive consolidation approach in 657 patients 17-60 years of age. Patients in first complete remission (CR1) after cytarabine and standard- or high-dose daunorubicin induction received 2 cycles of consolidation with high-dose cytarabine followed by peripheral blood progenitor cell collection. The 352 patients who entered consolidation were randomized to receive GO (n = 132) or not (n = 138) and then proceeded to autologous hematopoietic cell transplantation (HCT). GO was given to 67 patients. Median follow-up was 50.9 months. Results of the intention-to-treat analysis demonstrated a 4-year disease-free survival (DFS) of 33.6% versus 35.9% (P = .54) and an overall survival (OS) of 41.3% versus 41.9% (P = .52) for those randomized to receive GO versus no GO, respectively. Patients with favorable- and intermediate-risk acute myeloid leukemia (AML) treated with high-dose daunorubicin and autologous HCT had 4-year DFS rates of 60% and 40% and OS rates of 80% and 49.3%, respectively. For younger AML patients in CR1, autologous HCT should be considered in favorable- and intermediate-cytogenetic risk patients who do not have an allogeneic donor. The addition of a single dose of GO in this setting did not improve outcomes. This trial is registered at http://www.clinicaltrials.gov as NCT00049517.
机译:我们报告了一项前瞻性,随机第3期试验的结果,该试验评估了657名17-60岁的患者在强化强化治疗中使用吉妥单抗ozogamicin(GO)的情况。阿糖胞苷和标准剂量或大剂量柔红霉素诱导后首次完全缓解(CR1)的患者接受2次大剂量阿糖胞苷巩固治疗,然后收集外周血祖细胞。 352名进入巩固期的患者被随机分配接受GO(n = 132)或不接受GO(n = 138),然后进行自体造血细胞移植(HCT)。 GO被给予67例患者。中位随访时间为50.9个月。意向治疗分析结果显示4年无病生存率(DFS)为33.6%,而同期为35.9%(P = .54),总生存期(OS)为41.3%对41.9%(P =。 52)分别随机分配接受GO和不接受GO。大剂量柔红霉素和自体HCT治疗的具有中危和急性危险的急性髓细胞白血病(AML)患者的4年DFS率分别为60%和40%,OS率分别为80%和49.3%。对于CR1中较年轻的AML患者,对于没有同基因异体供体的有利和中等细胞遗传风险的患者,应考虑自体HCT。在这种情况下,单剂量的GO并不能改善预后。该试验已在http://www.clinicaltrials.gov上注册为NCT00049517。

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