首页> 美国卫生研究院文献>Haematologica >Age is a prognostic factor even among patients with multiple myeloma younger than 66 years treated with high-dose melphalan: the IFM experience on 2316 patients
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Age is a prognostic factor even among patients with multiple myeloma younger than 66 years treated with high-dose melphalan: the IFM experience on 2316 patients

机译:即使在接受大剂量美法仑治疗的多发性骨髓瘤小于66岁的患者中年龄也是预后因素:IFM在2316名患者中的经验

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摘要

Age is a strong prognostic factor in multiple myeloma. The overall survival is shorter in patients older than 66 years, and even shorter in those older than 75 years. Whether age is also a prognostic parameter in patients younger than 66 years treated homogeneously with intensive approaches is unknown. To address this issue, we retrospectively analyzed a series of 2316 patients treated homogeneously with 3–4 cycles of induction chemotherapy followed by a high-dose melphalan course, without any consolidation or maintenance. We show that patients older than 60 years have a statistically significant shorter overall survival. The analysis of prognostic parameters did not show a higher incidence of high-risk cytogenetics, but a higher incidence of International Staging System (ISS) stages 2 and 3, mainly due to higher β2-microglobulin levels. This study is the first to demonstrate the impact of age in the outcome of ‘young’ patients with multiple myeloma, and suggests that this parameter should be included in the stratification factors for future prospective clinical trials.
机译:年龄是多发性骨髓瘤的重要预后因素。超过66岁的患者的总生存期较短,而超过75岁的患者的总生存期甚至更短。不知道年龄是否也是接受强化治疗的66岁以下患者的预后参数。为了解决这个问题,我们回顾性分析了2316例接受3-4周期诱导化疗,随后大剂量美法仑疗程,没有任何巩固或维持的均等治疗的患者。我们显示,年龄超过60岁的患者的总体生存期在统计学上显着缩短。预后参数分析未显示高风险细胞遗传学的发生率较高,但国际分期系统(ISS)2和3期的发生率较高,这主要是由于较高的β2-微球蛋白水平所致。这项研究是第一个证明年龄对“年轻”多发性骨髓瘤患者预后的影响,并建议该参数应纳入分层因素中,以进行未来的前瞻性临床试验。

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