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Impact of structural severity on outcomes in knee osteoarthritis: an analysis of data from phase 2 and phase 3 lorecivivint clinical trials
被引:0
|作者:
Tambiah, Jeyanesh
[1
]
Kennedy, Sarah
[1
]
Swearingen, Christopher
[1
]
Mcalindon, Timothy
[2
]
Yazici, Yusuf
[1
,3
]
机构:
[1] Biosplice Therapeut Inc, 9360 Towne Ctr Dr, San Diego, CA 92121 USA
[2] Tufts Med Ctr, Boston, MA USA
[3] NYU Grossman Sch Med, New York, NY USA
来源:
关键词:
knee osteoarthritis;
DMOAD;
clinical trials;
structure-symptom relationship;
lorecivivint;
CLASSIFICATION;
JOINT;
INHIBITOR;
PAIN;
HIP;
D O I:
10.1093/rheumatology/keae610
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Objective: Developing knee osteoarthritis (OA) treatments is challenging due to assessing pain and joint structure outcomes within a highly heterogeneous disease. Lorecivivint (LOR), an intra-articular CLK/DYRK inhibitor, modulates Wnt and inflammatory pathways. This review analysis of LOR 0.07 mg trial data aims to describe the potential impact of baseline joint structure on OA pain response. Methods: Two Phase 2 and two Phase 3 trials enrolled knee OA patients with Kellgren-Lawrence (KL) Grades 2-3 and Pain Numeric Rating Scale [NRS (0-10)] >= 4 to <= 8 in their target knee. Cumulative frequency distribution plots by KL grade summarized the percentages of patients with medial joint space width (medial JSW) < 3 mm. Osteoarthritis Research Society International Joint Space Narrowing grades and treatment responses in trials capturing Pain NRS were similarly summarized. Pain outcome changes were estimated using baseline adjusted ANCOVA. Results: Compared with phase 2 trials, the phase 3 trials had an increased proportion of patients with baseline medial JSW <3 mm. LOR demonstrated beneficial treatment effects vs placebo in KL 2 subgroups, which were found to have higher proportions of baseline medial JSW >3 mm, apart from one Phase 3 trial with advanced structural knee OA. Conclusion: Baseline medial JSWs were heterogeneous across trials despite KL inclusion criteria. LOR demonstrated greater symptomatic improvements in patients with less structurally advanced disease, indicative of an association between OA structural damage and pain. Early treatment interventions may improve outcomes and provide insight for future OA trial inclusion criteria development.
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