From Spire Sciences Inc., Boca Raton, Florida; Albany Medical College and The Center for Rheumatology, Albany, New York; Geisel School of Medicine, Dartmouth College, Lebanon, New Hampshire; Case Western Reserve University and MetroHealth System, Cleveland, Ohio; Genentech Inc., South San Francisco, California, USA.
C. Peterfy, MD, Spire Sciences Inc.; J. Kremer, MD, Albany Medical College and The Center for Rheumatology; W. Rigby, MD, Geisel School of Medicine, Dartmouth College; N. Singer, MD, Case Western Reserve University and MetroHealth System; C. Birchwood, PhD, Genentech Inc.; D. Gill, BS, Genentech Inc.; W. Reiss, PharmD, Genentech Inc.; J. Pei, BS, Genentech Inc.; M. Michalska, MD, Genentech Inc.
J Rheumatol. 2020 Mar;47(3):325-332. doi: 10.3899/jrheum.180953. Epub 2019 Jun 1.
To assess differences in joint damage and inflammation using magnetic resonance imaging (MRI) between patients with rheumatoid arthritis (RA) who achieved low disease activity with tocilizumab (TCZ) + methotrexate (MTX) and subsequently continued or discontinued MTX.
In the COMP-ACT trial, US patients with RA received subcutaneous TCZ 162 mg + MTX. Those who achieved 28-joint count Disease Activity Score calculated with erythrocyte sedimentation rate (DAS28-ESR) ≤ 3.2 at Week 24 were randomized 1:1 (double-blind) to discontinue MTX (TCZ monotherapy; mono) or continue TCZ + MTX until Week 52. In a subset of patients, 1.5-Tesla MRI was used to obtain images of bilateral hands and wrists at weeks 24 and 40. Outcomes included changes in MRI-assessed synovitis, osteitis, erosion, and cartilage loss from Week 24 to Week 40, and in the proportion of patients with progression of each score.
Of 296 patients who achieved DAS28-ESR ≤ 3.2 at Week 24, 79 were enrolled in the pilot MRI substudy and randomized to TCZ mono (n = 38) or TCZ + MTX (n = 41). Treatment with either TCZ mono or TCZ + MTX suppressed erosion progression, synovitis, osteitis, and cartilage loss. The proportion of patients with no progression in each outcome measure was similar between groups (range, TCZ mono: 84.8-97.0%; TCZ + MTX: 92.3-100%).
In a subset of patients who achieved low disease activity with TCZ + MTX, MRI changes were minimal in intraarticular inflammation and damage measures in patients who discontinued MTX versus those who continued TCZ + MTX.
评估接受托珠单抗(TCZ)+甲氨蝶呤(MTX)治疗达到低疾病活动度的类风湿关节炎(RA)患者,继续或停用 MTX 后在关节损伤和炎症方面的磁共振成像(MRI)差异。
在 COMP-ACT 试验中,美国 RA 患者接受 TCZ 162mg 皮下注射+MTX。在第 24 周时达到红细胞沉降率(ESR)校正的 28 关节疾病活动度评分(DAS28-ESR)≤3.2 的患者,按 1:1(双盲)随机分为停用 MTX(TCZ 单药治疗;单药组)或继续 TCZ+MTX 至第 52 周。在患者亚组中,在第 24 周和第 40 周使用 1.5T MRI 获得双侧手和腕部图像。主要终点是第 24 周至第 40 周 MRI 评估的滑膜炎、骨炎、侵蚀和软骨丢失的变化,以及每个评分进展的患者比例。
在 296 例达到第 24 周 DAS28-ESR≤3.2 的患者中,有 79 例入组了探索性 MRI 子研究并随机分为 TCZ 单药(n=38)或 TCZ+MTX(n=41)。TCZ 单药或 TCZ+MTX 治疗均抑制了侵蚀进展、滑膜炎、骨炎和软骨丢失。两组间每个结局指标无进展的患者比例相似(范围,TCZ 单药:84.8%-97.0%;TCZ+MTX:92.3%-100%)。
在 TCZ+MTX 达到低疾病活动度的患者亚组中,与继续 TCZ+MTX 相比,停用 MTX 患者的关节内炎症和损伤指标的 MRI 变化较小。