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卡非佐米、来那度胺和地塞米松治疗复发多发性骨髓瘤。

Carfilzomib, lenalidomide, and dexamethasone for relapsed multiple myeloma.

机构信息

The authors' affiliations are listed in the Appendix.

出版信息

N Engl J Med. 2015 Jan 8;372(2):142-52. doi: 10.1056/NEJMoa1411321. Epub 2014 Dec 6.

Abstract

BACKGROUND

Lenalidomide plus dexamethasone is a reference treatment for relapsed multiple myeloma. The combination of the proteasome inhibitor carfilzomib with lenalidomide and dexamethasone has shown efficacy in a phase 1 and 2 study in relapsed multiple myeloma.

METHODS

We randomly assigned 792 patients with relapsed multiple myeloma to carfilzomib with lenalidomide and dexamethasone (carfilzomib group) or lenalidomide and dexamethasone alone (control group). The primary end point was progression-free survival.

RESULTS

Progression-free survival was significantly improved with carfilzomib (median, 26.3 months, vs. 17.6 months in the control group; hazard ratio for progression or death, 0.69; 95% confidence interval [CI], 0.57 to 0.83; P=0.0001). The median overall survival was not reached in either group at the interim analysis. The Kaplan-Meier 24-month overall survival rates were 73.3% and 65.0% in the carfilzomib and control groups, respectively (hazard ratio for death, 0.79; 95% CI, 0.63 to 0.99; P=0.04). The rates of overall response (partial response or better) were 87.1% and 66.7% in the carfilzomib and control groups, respectively (P<0.001; 31.8% and 9.3% of patients in the respective groups had a complete response or better; 14.1% and 4.3% had a stringent complete response). Adverse events of grade 3 or higher were reported in 83.7% and 80.7% of patients in the carfilzomib and control groups, respectively; 15.3% and 17.7% of patients discontinued treatment owing to adverse events. Patients in the carfilzomib group reported superior health-related quality of life.

CONCLUSIONS

In patients with relapsed multiple myeloma, the addition of carfilzomib to lenalidomide and dexamethasone resulted in significantly improved progression-free survival at the interim analysis and had a favorable risk-benefit profile. (Funded by Onyx Pharmaceuticals; ClinicalTrials.gov number, NCT01080391.).

摘要

背景

来那度胺联合地塞米松是复发性多发性骨髓瘤的标准治疗方案。蛋白酶体抑制剂卡非佐米与来那度胺和地塞米松联合应用在复发性多发性骨髓瘤的 1 期和 2 期研究中显示出疗效。

方法

我们将 792 例复发性多发性骨髓瘤患者随机分为卡非佐米联合来那度胺和地塞米松(卡非佐米组)或来那度胺和地塞米松单药治疗(对照组)。主要终点是无进展生存期。

结果

卡非佐米组的无进展生存期显著改善(中位无进展生存期 26.3 个月,对照组为 17.6 个月;进展或死亡风险比为 0.69;95%置信区间[CI],0.57 至 0.83;P=0.0001)。中期分析时,两组均未达到中位总生存期。卡非佐米组和对照组的 Kaplan-Meier 24 个月总生存率分别为 73.3%和 65.0%(死亡风险比为 0.79;95%CI,0.63 至 0.99;P=0.04)。卡非佐米组和对照组的总缓解率(部分缓解或更好)分别为 87.1%和 66.7%(P<0.001;分别有 31.8%和 9.3%的患者获得完全缓解或更好;分别有 14.1%和 4.3%的患者获得严格的完全缓解)。卡非佐米组和对照组分别有 83.7%和 80.7%的患者发生 3 级或更高级别的不良事件;分别有 15.3%和 17.7%的患者因不良事件停止治疗。卡非佐米组患者的健康相关生活质量更好。

结论

在复发性多发性骨髓瘤患者中,与来那度胺和地塞米松联合应用卡非佐米可显著提高无进展生存期,并具有良好的风险效益比。(由 Onyx Pharmaceuticals 资助;ClinicalTrials.gov 编号,NCT01080391。)

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