首页> 外文期刊>Journal of Clinical Oncology >High-dose therapy and autologous blood stem-cell transplantation compared with conventional treatment in myeloma patients aged 55 to 65 years: long-term results of a randomized control trial from the Group Myelome-Autogreffe.
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High-dose therapy and autologous blood stem-cell transplantation compared with conventional treatment in myeloma patients aged 55 to 65 years: long-term results of a randomized control trial from the Group Myelome-Autogreffe.

机译:在55至65岁的骨髓瘤患者中,大剂量疗法和自体血干细胞移植与常规疗法相比:Myelome-Autogreffe组的一项随机对照试验的长期结果。

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PURPOSE: To study the impact of high-dose therapy (HDT) with autologous stem-cell support in patients with symptomatic multiple myeloma (MM) between the ages of 55 and 65 years. PATIENTS AND METHODS: One hundred ninety patients between 55 and 65 years old who had newly diagnosed stage II or III MM were randomly assigned to receive either conventional chemotherapy (CCT; ie, monthly courses of a regimen of vincristine, melphalan, cyclophosphamide, and prednisone) or HDT and autologous blood stem-cell transplantation (using either melphalan alone 200 mg/m(2) intravenous [IV] or melphalan 140 mg/m(2) IV plus busulfan 16 mg/kg orally as pretransplantation cytoreduction). RESULTS: Within a median follow-up of 120 months, median event-free survival (EFS) times were 25 and 19 months in the HDT and CCT groups, respectively. Median overall survival (OS) time was 47.8 months in the HDT group compared with 47.6 months in the CCT group. A trend to better EFS (P = .07) was observed in favor of HDT, whereas OS curves were not statistically different (P = .91). The period of time without symptoms, treatment, and treatment toxicity (TwiSTT) was significantly longer for the HDT patients than for the CCT patients (P = .03). CONCLUSION: With a median follow-up time of approximately 10 years, this randomized trial confirmed a benefit of HDT in terms of EFS and TwiSTT but did not provide evidence for superiority of HDT over CCT in OS of patients aged 55 to 65 years with symptomatic newly diagnosed MM.
机译:目的:研究自体干细胞支持大剂量治疗(HDT)对55岁至65岁有症状多发性骨髓瘤(MM)患者的影响。患者与方法:随机将新诊断为II或III期MM的190名55至65岁的患者随机分配接受常规化疗(CCT;即长春新碱,美法仑,环磷酰胺和泼尼松方案的每月疗程) )或HDT和自体血干细胞移植(单独使用美法仑200 mg / m(2)静脉注射[IV]或美法仑140 mg / m(2)IV加白消安16 mg / kg口服作为移植前的细胞减少作用)。结果:在平均随访120个月内,HDT和CCT组的无事件生存(EFS)时间中位数分别为25和19个月。 HDT组中位总生存(OS)时间为47.8个月,而CCT组为47.6个月。观察到EFS改善的趋势(P = .07),有利于HDT,而OS曲线无统计学差异(P = .91)。 HDT患者的无症状,治疗和治疗毒性(TwiSTT)的时间明显长于CCT患者(P = .03)。结论:平均随访时间约为10年,该随机试验证实了HDT在EFS和TwiSTT方面的益处,但未提供证据表明55至65岁有症状患者的HDT优于CCT新诊断的MM。

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