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Effect of Romosozumab Treatment in Postmenopausal Women With Osteoporosis and Knee Osteoarthritis: Results From a Substudy of a Phase 3 Clinical Trial.
Lane, Nancy E; Betah, Donald; Deignan, Cynthia; Oates, Mary; Wang, Zhenxun; Timoshanko, Jen; Khan, Aliya A; Binkley, Neil.
Afiliação
  • Lane NE; University of California, Davis Health, Sacramento.
  • Betah D; Amgen Inc, Thousand Oaks, California.
  • Deignan C; Amgen Inc, Thousand Oaks, California.
  • Oates M; Amgen Inc, Thousand Oaks, California.
  • Wang Z; Amgen Inc, Thousand Oaks, California.
  • Timoshanko J; UCB Pharma, Slough, UK.
  • Khan AA; McMaster University, Oakville, Ontario, Canada.
  • Binkley N; University of Wisconsin-, Madison.
ACR Open Rheumatol ; 6(1): 43-51, 2024 Jan.
Article em En | MEDLINE | ID: mdl-37985218
ABSTRACT

OBJECTIVE:

Romosozumab is a bone-forming agent approved for osteoporosis treatment. Here we report results of the protocol-specified, noninferiority osteoarthritis substudy of the fracture study in postmenopausal women with osteoporosis (FRAME), which evaluated the effect of romosozumab versus placebo on knee osteoarthritis in patients with a clinical history of osteoarthritis.

METHODS:

Women in FRAME with a history of knee osteoarthritis were eligible for enrollment in the osteoarthritis substudy; key inclusion criteria were osteoarthritis-related signal knee pain, morning stiffness lasting less than 30 minutes, knee crepitus, and knee osteoarthritis confirmed by x-ray within 12 months. The protocol-specified outcomes were change from baseline through month 12 in the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score, incidence of worsening knee osteoarthritis, and treatment-emergent adverse events (TEAEs) with romosozumab versus placebo. In a post hoc analysis, percentage change from baseline to month 12 in bone mineral density (BMD) was assessed.

RESULTS:

Of 7180 women in FRAME, 347 participated in the osteoarthritis substudy (placebo, 177; romosozumab, 170). At month 12, no significant difference in progression of knee osteoarthritis was observed with romosozumab versus placebo (least squares mean total WOMAC score -2.2 vs. -1.3; P = 0.71). Incidence of worsening symptoms of knee osteoarthritis was comparable between romosozumab (17.1%) and placebo (20.5%) (odds ratio 0.9 [95% confidence interval 0.5, 1.7]; P = 0.69). Incidence of TEAEs of osteoarthritis was numerically lower with romosozumab (13 [7.7%]) versus placebo (21 [12.0%]). BMD gains were higher with romosozumab.

CONCLUSION:

Romosozumab treatment did not impact knee pain or function in postmenopausal women with osteoporosis and knee osteoarthritis and resulted in significant BMD gains in these women.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article