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Carfilzomib, Lenalidomide, and Dexamethasone for Relapsed Multiple Myeloma

Carfilzomib公司 来那度胺 医学 地塞米松 多发性骨髓瘤 肿瘤科 蛋白酶体抑制剂 内科学 药理学
作者
A. Keith Stewart,S. Vincent Rajkumar,Meletios Α. Dimopoulos,Tamás Masszi,Ivan Špıčka,Albert Oriol,Roman Hájek,Laura Rosiñol,David S. Siegel,Georgi Mihaylov,Vesselina Goranova‐Marinova,Péter Rajnics,Aleksandr Suvorov,Rubén Niesvizky,Andrzej Jakubowiak,Jesús F. San Miguel,Heinz Ludwig,Michael Wang,Vladimír Maisnar,Jiří Minařík,William I. Bensinger,María-Victoria Mateos,Dina Ben‐Yehuda,Vishal Kukreti,Naseem J. Zojwalla,Margaret Tonda,Xinqun Yang,Biao Xing,Philippe Moreau,Antonio Palumbo
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:372 (2): 142-152 被引量:1168
标识
DOI:10.1056/nejmoa1411321
摘要

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.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.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.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.).
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