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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Complete response correlates with long-term progression-free and overall survival in elderly myeloma treated with novel agents: analysis of 1175 patients.
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Complete response correlates with long-term progression-free and overall survival in elderly myeloma treated with novel agents: analysis of 1175 patients.

机译:完全缓解与使用新型药物治疗的老年骨髓瘤的长期无进展生存率和总体生存率相关:分析1175例患者。

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摘要

Complete response (CR) was an uncommon event in elderly myeloma patients until novel agents were combined with standard oral melphalan-prednisone. This analysis assesses the impact of treatment response on progression-free survival (PFS) and overall survival (OS). We retrospectively analyzed 1175 newly diagnosed myeloma patients, enrolled in 3 multicenter trials, treated with melphalan-prednisone alone (n = 332), melphalan-prednisone-thalidomide (n = 332), melphalan-prednisone-bortezomib (n = 257), or melphalan-prednisone-bortezomib-thalidomide (n = 254). After a median follow-up of 29 months, the 3-year PFS and OS were 67% and 27% (hazard ratio = 0.16; P < .001), and 91% and 70% (hazard ratio = 0.15; P < .001) in patients who obtained CR and in those who achieved very good partial response, respectively. Similar results were observed in patients older than 75 years. Multivariate analysis confirmed that the achievement of CR was an independent predictor of longer PFS and OS, regardless of age, International Staging System stage, and treatment. These findings highlight a significant association between the achievement of CR and long-term outcome, and support the use of novel agents to achieve maximal response in elderly patients, including those more than 75 years. This trial was registered at www.clinicaltrials.gov as #NCT00232934, #ISRCTN 90692740, and #NCT01063179.
机译:完全缓解(CR)在老年骨髓瘤患者中很少见,直到将新型药物与标准口服美法仑-泼尼松联合使用为止。该分析评估了治疗反应对无进展生存期(PFS)和总体生存期(OS)的影响。我们回顾性分析了1175例新诊断的骨髓瘤患者,这些患者参加了3项多中心试验,分别接受美法仑-泼尼松-n = 332,美法仑-泼尼松-沙利度胺(n = 332),美法仑-泼尼松-硼替佐米(n = 257)或美法仑-泼尼松-硼替佐米-沙利度胺(n = 254)。中位随访29个月后,3年PFS和OS分别为67%和27%(危险比= 0.16; P <.001),91%和70%(危险比= 0.15; P <)。 001)获得CR的患者和获得非常良好的部分缓解的患者。在75岁以上的患者中观察到类似的结果。多变量分析证实,无论年龄,国际分期系统的分期和治疗情况如何,CR的获得是PFS和OS更长的独立预测指标。这些发现强调了CR的实现与长期结局之间的显着关联,并支持使用新型药物在包括75岁以上的老年患者中获得最大的反应。该试验已在www.clinicaltrials.gov上注册为#NCT00232934,#ISRCTN 90692740和#NCT01063179。

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