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首页> 外文期刊>Haematologica >Comparison of intensive chemotherapy, allogeneic or autologous stem cell transplantation as post-remission treatment for adult patients with high-risk acute lymphoblastic leukemia. Results of the PETHEMA ALL-93 trial | Haematologica
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Comparison of intensive chemotherapy, allogeneic or autologous stem cell transplantation as post-remission treatment for adult patients with high-risk acute lymphoblastic leukemia. Results of the PETHEMA ALL-93 trial | Haematologica

机译:成人高危急性淋巴细胞白血病成人患者接受强化化疗,同种异体或自体干细胞移植作为缓解后治疗的比较。 PETHEMA ALL-93试验的结果|血液学

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BACKGROUND AND OBJECTIVES: The optimal post-remission therapy for adults with high-risk acute lymphoblastic leukemia (ALL) is not well established. This multicenter randomized trial by the Spanish PETHEMA Group was addressed to compare three options of post-remission therapy in adults with high-risk ALL: chemotherapy, allogeneic stem cell transplantation (SCT) and autologous SCT. DESIGN AND METHODS: A total of 222 valid high-risk ALL patients entered the trial. All received a standard five-drug/five-week induction course. Patients in complete remission with an HLA-identical family donor were assigned to allogeneic SCT (n=84) and the remaining were randomized to autologous SCT (n=50) or to delayed intensification followed by maintenance chemotherapy up to 2 years in complete remission (n=48). RESULTS: Overall, 183 patients achieved complete remission (82%). With a median follow-up of 70 months, the median disease-free survival and overall survival were 17 and 23 months, respectively. The 5-year disease-free survival and overall survival were 35% (95% CI, 30%-41%) and 34% (95% CI, 28%-39%), respectively. Patients allocated to the chemotherapy, allogeneic and autologous SCT were comparable in the main pre-treatment ALL characteristics and the rate of response to therapy. Intention-to-treat analysis showed no differences between patients according to whether they had or did not have a donor in disease-free survival (39%, 95% CI 30-48% vs. 33%, 95% CI 23-41%) and overall survival (44%, 95% CI 35-52% vs. 35%, 95% CI 25-44%), as well as for autologous SCT vs. chemotherapy comparisons (disease-free survival: 40%, 95% CI 28-52% vs. 51%, 95% CI 37-67%; overall survival: 43%, 95% CI 29-58% vs. 52%, 95% CI 39-65%). No differences were observed when the analysis was made on the basis of the treatment actually performed. INTERPRETATION AND CONCLUSIONS: This study failed to prove that, when a family donor is available, allogeneic SCT produces a better outcome than autologous SCT or chemotherapy in adults with high-risk ALL.
机译:背景与目的:对于成人高危急性淋巴细胞白血病(ALL)的最佳缓解后治疗方法尚不完善。西班牙PETHEMA集团进行的这项多中心随机试验旨在比较高危ALL患者缓解后治疗的三种选择:化学疗法,同种异体干细胞移植(SCT)和自体SCT。设计与方法:共有222名有效的高危ALL患者进入了试验。所有人都接受了标准的五药/五周诱导课程。 HLA完全相同的家庭供者完全缓解的患者被分配到同种异体SCT(n = 84),其余患者被随机分配到自体SCT(n = 50)或延迟强化治疗,然后维持化疗直至完全缓解2年( n = 48)。结果:总体上,有183例患者完全缓解(82%)。中位随访70个月,中位无病生存期和总生存期分别为17个月和23个月。 5年无病生存期和总生存期分别为35%(95%CI,30%-41%)和34%(95%CI,28%-39%)。分配给化疗,同种异体和自体SCT的患者在主要的治疗前ALL特征和对治疗的反应率方面具有可比性。意向治疗分析显示,根据患者是否有供体,无病生存期之间无差异(39%,95%CI 30-48%,33%,95%CI 23-41% )和总体生存率(44%,95%CI 35-52%vs. 35%,95%CI 25-44%),以及自体SCT与化疗的比较(无疾病生存期:40%,95% CI 28-52%对比51%,95%CI 37-67%;总生存期:43%,95%CI 29-58%与52%,95%CI 39-65%)。当基于实际进行的处理进行分析时,未观察到差异。解释和结论:这项研究未能证明,在有家庭供体的情况下,同种异体SCT的结果比自体SCT或高危ALL成人化疗效果更好。

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