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二十一世纪多发性骨髓瘤患者生存率提高的模式:一项基于人群的研究。

Patterns of improved survival in patients with multiple myeloma in the twenty-first century: a population-based study.

机构信息

Department of Medicine, Section of Hematology, Malmö University Hospital, S-2052 Malmö, Sweden.

出版信息

J Clin Oncol. 2010 Feb 10;28(5):830-4. doi: 10.1200/JCO.2009.25.4177. Epub 2009 Dec 28.

Abstract

PURPOSE Randomized multiple myeloma (MM) studies show improved response rates and better progression-free survival for newer therapies. However, a less pronounced effect has been found for overall survival (OS). Using population-based data including detailed treatment information for individual patients, we assessed survival patterns for all patients diagnosed with MM in Malmö, Sweden from 1950 to 2005. PATIENTS AND METHODS We identified 773 patients with MM (48% males). On the basis of the age limit used for treatment with high-dose melphalan with autologous stem-cell support (HDM-ASCT; < or = 65 years old) in Sweden, we constructed Kaplan-Meier curves and used the Breslow generalized Wilcoxon test to evaluate OS patterns (diagnosed in six calendar periods) for patients 65 years old or younger and patients older than 65 years. Results Including all age groups, patients diagnosed from 1960 to 1969 had a better survival than patients diagnosed from 1950 to 1959. In subsequent 10-year calendar periods, median OS increased from 24.3 to 56.3 months (P = .036) in patients < or = 65 years old. In contrast, OS did not improve among patients older than age 65 years (21.2 to 26.7 months, P = .7). CONCLUSION With the establishment of HDM-ASCT as the standard therapy for younger patients with MM, OS has improved significantly for this age group in the general MM population. With novel therapies being commonly used at disease progression, presumably it becomes increasingly difficult to confirm survival differences between defined induction, consolidation, and maintenance therapies in the future. Consequently, in the era of novel MM therapies, population-based studies will serve as a necessary complement to randomized trials.

摘要

目的

随机多发性骨髓瘤(MM)研究表明,新型疗法可提高缓解率和无进展生存期,但对总生存期(OS)的影响较小。利用包括个体患者详细治疗信息的基于人群的数据,我们评估了 1950 年至 2005 年在瑞典马尔默诊断为 MM 的所有患者的生存模式。

患者和方法

我们确定了 773 例 MM 患者(48%为男性)。基于在瑞典使用大剂量美法仑联合自体干细胞支持(HDM-ASCT;<或=65 岁)治疗的年龄限制,我们构建了 Kaplan-Meier 曲线,并使用 Breslow 广义 Wilcoxon 检验评估了 65 岁及以下和>65 岁患者的 OS 模式(在六个日历期间诊断)。

结果

包括所有年龄组,1960 年至 1969 年诊断的患者比 1950 年至 1959 年诊断的患者生存更好。在随后的 10 年日历期间,<或=65 岁的患者的中位 OS 从 24.3 个月增加到 56.3 个月(P=0.036)。相比之下,>65 岁的患者的 OS 并未改善(21.2 至 26.7 个月,P=0.7)。

结论

随着 HDM-ASCT 作为年轻 MM 患者的标准治疗方法的确立,该年龄组在一般 MM 人群中的 OS 显著改善。随着新型疗法在疾病进展时普遍使用,未来可能越来越难以确认明确的诱导、巩固和维持治疗之间的生存差异。因此,在新型 MM 疗法时代,基于人群的研究将成为随机试验的必要补充。

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