INSURE: a pooled analysis of ixazomib-lenalidomide-dexamethasone for relapsed/refractory myeloma in routine practice

被引:1
|
作者
Leleu, Xavier [1 ]
Lee, Hans C. [2 ]
Zonder, Jeffrey A. [3 ]
Macro, Margaret [4 ]
Ramasamy, Karthik [5 ]
Hulin, Cyrille [6 ]
Silar, Jiri [7 ]
Kuhn, Matyas [7 ]
Ren, Kaili [8 ]
Bent-Ennakhil, Nawal [9 ]
Cherepanov, Dasha [8 ]
Stull, Dawn Marie [10 ]
Terpos, Evangelos [11 ]
机构
[1] CHU La Miletrie Poitiers, Dept Hematol, Pole Reg Cancerol, F-86000 Poitiers, France
[2] MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] Wayne State Univ, Barbara Ann Karmanos Canc Inst, Sch Med, Detroit, MI 48201 USA
[4] CHU Caen, F-14000 Caen, France
[5] Oxford Univ Hosp NHS Fdn Trust, Dept Haematol, Oxford OX3 7LE, Oxon, England
[6] CHU Bordeaux, F-33000 Bordeaux, France
[7] Inst Biostat & Anal Ltd, Brno 60200, Czech Republic
[8] Takeda Dev Ctr Amer Inc TDCA, Lexington, MA 02421 USA
[9] Takeda Pharmaceut Int AG, CH-8152 Opfikon, Switzerland
[10] Takeda Pharmaceut USA Inc, Lexington, MA 02421 USA
[11] Natl & Kapodistrian Univ Athens, Sch Med, Dept Clin Therapeut, Athens, Greece
关键词
effectiveness; ixazomib; ixazomib-lenalidomide-dexamethasone; IRd; multiple myeloma; pooled analysis; progression-free survival; proteasome inhibitor; relapsed/refractory; routine clinical practice; time-to-next treatment; MULTIPLE-MYELOMA; SURVIVAL; BORTEZOMIB; DURATION; THERAPY;
D O I
10.2217/fon-2023-0604
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: We pooled data from three observational studies (INSIGHT MM, UVEA-IXA and REMIX) to investigate the real-world effectiveness of ixazomib-lenalidomide-dexamethasone (IRd) in relapsed/refractory myeloma. Materials & methods: INSIGHT MM was a prospective study conducted in countries across Europe, Asia and North/Latin America while UVEA-IXA and REMIX were multicenter, retrospective/prospective studies conducted in Europe. Patients who had received IRd as >= 2nd line of therapy were analyzed. Primary outcomes were time-to-next treatment (TTNT) and progression-free survival (PFS). Results: Overall, 564 patients were included (median follow-up: 18.5 months). Median TTNT and PFS were 18.4 and 19.9 months; both outcomes were numerically longer for earlier versus later lines. Median treatment duration was 14.0 months. Overall response rate was 64.6%. No new safety concerns were noted. Conclusion: The effectiveness of IRd in routine practice appears similar to the efficacy observed in TOURMALINE-MM1. IRd benefit in earlier versus later lines was consistent with previous reports.
引用
收藏
页码:935 / 950
页数:16
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