The effects of different schedules of bortezomib, melphalan, and prednisone for patients with newly diagnosed multiple myeloma who are transplant ineligible: a matching-adjusted indirect comparison

被引:10
|
作者
Mateos, Maria-Victoria [1 ]
San-Miguel, Jesus [2 ]
Goldschmidt, Hartmut [3 ,4 ]
Sonneveld, Pieter [5 ]
Dimopoulos, Meletios A. [6 ]
Heeg, Bart [7 ]
Hashim, Mahmoud [7 ]
Deraedt, William [8 ]
Hu, Peter [9 ]
Lam, Annette [10 ]
He, Jianming [10 ]
机构
[1] Univ Hosp Salamanca, IBSAL, Haematol Dept, Salamanca, Spain
[2] Clin Univ Navarra, CIMA, IDISNA, CIBERONC, Pamplona, Spain
[3] Univ Clin Heidelberg, Internal Med 5, Heidelberg, Germany
[4] Univ Clin Heidelberg, Natl Ctr Tumor Dis NCT, Heidelberg, Germany
[5] Erasmus MC, Dept Haematol, Rotterdam, Netherlands
[6] Natl & Kapodistrian Univ Athens, Dept Clin Therapeut, Athens, Greece
[7] Ingress Hlth, Rotterdam, Netherlands
[8] Janssen Res & Dev, Oncol R&D, Beerse, Belgium
[9] Janssen Res & Dev LLC, Stat Programming Haematol, Raritan, NJ USA
[10] Janssen Global Serv LLC, Global Market Access & Hlth Policy, Raritan, NJ USA
关键词
VMP; multiple myeloma; matching-adjusted indirect comparison; PERIPHERAL NEUROPATHY; INITIAL TREATMENT; PLUS MELPHALAN; EFFICACY; MAINTENANCE; THALIDOMIDE; SURVIVAL; OUTCOMES; REVERSIBILITY; ADALIMUMAB;
D O I
10.1080/10428194.2019.1675881
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
For patients with newly diagnosed multiple myeloma (NDMM) who are transplant ineligible, bortezomib-melphalan-prednisone (VMP) demonstrated superior efficacy based on the VISTA trial. In subsequent trials, twice-weekly bortezomib was limited to the first cycle or completely replaced with once-weekly bortezomib to reduce toxicity. Following a systematic literature review, the efficacy and safety of modified VMP schedules (pooled data from the once-weekly bortezomib VMP arm of the GIMEMA trial and the VMP arm of the ALCYONE trial) were compared to the VISTA schedule using naive and unanchored matching-adjusted indirect comparison (MAIC). Median progression-free survival was similar between VISTA and modified VMP (20.7 months [95% CI, 18.4-24.3] vs 19.6 months [95% CI, 18.8-21.0]). Peripheral neuropathy was significantly reduced with modified VMP versus VISTA VMP (all grades: naive, 32.1% vs 46.8% and MAIC, 32.1% vs 46.7%; both p < .0001). These findings support a modified VMP dosing schedule for patients with NDMM who are transplant ineligible.
引用
收藏
页码:680 / 690
页数:11
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