Symptomatic benefit of momelotinib in patients with myelofibrosis: Results from the SIMPLIFY phase III studies

被引:9
|
作者
Mesa, Ruben A. [1 ,18 ]
Hudgens, Stacie [2 ]
Floden, Lysbeth [2 ]
Harrison, Claire N. [3 ]
Palmer, Jeanne [4 ]
Gupta, Vikas [5 ]
McLornan, Donal P.
McMullin, Mary F. [6 ]
Kiladjian, Jean-Jaques [7 ]
Foltz, Lynda [8 ]
Platzbecker, Uwe [9 ]
Fox, M. Laura [10 ]
Mead, Adam J. [11 ]
Ross, David M. [12 ]
Oh, Stephen T. [13 ]
Perkins, Andrew [14 ]
Leahy, Michael F. [15 ]
Deheshi, Samineh [16 ]
Donahue, Rafe [16 ]
Klencke, Barbara J.
Verstovsek, Srdan [17 ]
机构
[1] Wake Forest Univ, Atrium Hlth Wake Forest Baptist Comprehens Canc Ct, Sch Med, Winston Salem, NC USA
[2] Clin Outcomes Solut, Tucson, AZ USA
[3] Guys & St Thomas NHS Fdn Trust, London, England
[4] Mayo Clin, Phoenix, AZ USA
[5] Univ Toronto, Univ Hlth Network, Toronto, ON, Canada
[6] Queens Univ, Belfast City Hosp Trust, Belfast, North Ireland
[7] Univ Paris, Hop St Louis, Paris, France
[8] Univ British Columbia, St Pauls Hosp, Vancouver, BC, Canada
[9] Leipzig Univ Hosp, Leipzig, Germany
[10] Hosp Univ Vall dHebron, Vall dHebron Barcelona Hosp Campus, Vall dHebron Inst Oncol VHIO,Experimental Hematol, Hematol Dept, Barcelona, Spain
[11] MRC Weatherall Inst Mol Med, Oxford, England
[12] Flinders Med Ctr & Univ, Adelaide, SA, Australia
[13] Washington Univ, Sch Med, St Louis, MO USA
[14] Monash Univ, Alfred Hosp, Melbourne, Vic, Australia
[15] Univ Western Australia, Perth, WA, Australia
[16] Sierra Oncol, Plymouth, MI USA
[17] MD Anderson Canc Ctr, Houston, TX USA
[18] Wake Forest Univ, Atrium Hlth Wake Forest Baptist Comprehens Canc Ct, Sch Med, Med Ctr Blvd,11th Floor, Winston Salem, NC 27157 USA
来源
CANCER MEDICINE | 2023年 / 12卷 / 09期
关键词
JAK inhibitor; momelotinib; myelofibrosis; patient-reported outcomes; symptoms; AVAILABLE THERAPY; RUXOLITINIB; TRIAL;
D O I
10.1002/cam4.5799
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Myelofibrosis (MF)-associated constitutional symptoms can severely impact health-related quality of life. Clinical trials in MF traditionally measure symptom response to treatment as a landmark endpoint of total symptom score (TSS) reduction =50% from baseline. However, this dichotomous assessment provides a limited view of clinically relevant symptomatic changes. Herein we evaluated longitudinal change from baseline in TSS over the continuous 24-week period and individual symptom scores to obtain a more comprehensive understanding of symptom benefits experienced by patients with MF receiving therapy.Methods: Longitudinal symptom change was evaluated using mixed-effect model repeated measure (MMRM) methodology with individual item-level analyses to complement the interpretation of the landmark symptom results in the completed phase III SIMPLIFY studies of momelotinib in MF. MMRM compared mean change in TSS from baseline with Week 24 using data from all patient visits. Generalized estimating equations were used to estimate item-level odds ratios using multiple predictive imputations for missing data.Results: Momelotinib and ruxolitinib groups reported similar overall symptom improvements, with a TSS difference of <1.5 points between groups for each post-baseline visit in SIMPLIFY-1. In SIMPLIFY-2, the improvement in TSS observed in momelotinib-treated patients was consistent with that observed in SIMPLIFY-1, whereas progressive TSS deterioration was observed with control. Item-level scores were heterogeneous in both studies. A similar and greater proportion of momelotinib-treated patients were categorized as "improved" or "stable" compared with control in SIMPLIFY-1 and SIMPLIFY-2, respectively. Odds ratios for between-group comparison ranged from 0.75 to 1.21 in SIMPLIFY-1, demonstrating similarity in likelihood of symptom improvement. In SIMPLIFY-2, the likelihood of symptom improvement in each item was higher in the momelotinib arm.Conclusions: These findings suggest that momelotinib provides clinically relevant symptom benefits in the JAK inhibitor-naive and JAK inhibitor-exposed settings.
引用
收藏
页码:10612 / 10624
页数:13
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