Poster Session B
Myopathic rheumatic diseases (polymyositis, dermatomyositis, inclusion body myositis)
Xia Lyu, MD (she/her/hers)
Department of Rheumatology, Renji Hospital, Shanghai Jiaotong University School of Medicine
Shanghai, Shanghai, China
No financial relationships with ineligible companies to disclose
B cell depletion in the form of rituximab (RTX) is an established treatment modality for idiopathic inflammatory myopathies (IIM). Treatment response is now assessed in myositis clinical trials using the internationally accepted Total Improvement Score (TIS). Data using TIS regarding RTX response in IIM remains lacking.
Methods:
The MYOPROSP is a prospective observational cohort study that enrolled adult IIM cases from 23 centres in the UK during 2016-2020. We reviewed the registry to identify cases where RTX was initially administered or restarted. We also identified control cases who entered the registry during the same period but never received RTX matched by their myositis subgroups. The International Myositis Assessment and Clinical Studies Group (IMACS) core set measures were collected to generate TIS. The interval for the RTX group was limited to 60-200 days. Baseline characteristics were compared using t-test or Fisher’s exact test. Univariate logistic regression was first applied to compare response rate. Baseline covariates were balanced following the multiple imputations and inverse probability of treatment weighting (Figure 2A). Data were adjusted for concomitant drug number, average steroid dose, and follow-up interval using multivariate logistic regression.
Results:
Sixty-three patients in MYOPROSP initiated or restarted RTX; 42 with computable TIS met the interval requirement. 93 controls were identified, among which 51 had a change in therapy around baseline. The RTX group was significantly younger at diagnosis and enrollment and had a longer disease duration (Table 1). There were no significant differences in gender distribution, BMI, clinical manifestations, or baseline oral steroid doses. The RTX group failed more treatment compared to the controls. Baseline physician global activity, patient global activity, and extra-muscular activity were significantly higher in the RTX group. During a median 128-day follow-up, the rituximab group had a higher TIS (median 32.50 [interquartile range 17.5-46.9] RTX vs. 17.5[7.5-40.0] controls). 30/42 (71.4%) RTX patients vs. 44/93 (47.3%) controls (Odds Ratio (OR) 2.78, 95% Confidence Interval (CI) 1.27-6.09, p=0.01, univariate logistic regression) achieved at least minimal improvement (Figure 1). However, on applying multivariate analysis, the association no longer reached statistical significance (pooled OR 3.78, 95% CI 2.57-24.92, p=0.17) (Figure 2B).
Conclusion:
Using TIS in an observational setting, we have demonstrated that patients receiving RTX are more likely to respond to treatment than patients receiving conventional immunosuppressants, despite them having longer disease duration and failing more therapies.
Table 1: Overall Baseline Data and Comparison Between the Rituximab Group and Controls. N, number of non-missing values; yo, year-old; *, p <0.05. ASyS, anti-synthetase syndrome; DM, dermatomyositis; IMNM, immune-mediated necrotizing myopathies; OM, overlap myositis. PGA, patient global assessment; PhGA, physician global assessment; MMT-8, Manual Muscle Testing-8 score; VAS, visual analogue scale.
Figure 1: case selection procedure and response results
Figure 2: (A) Love plot showing covariate balance before and after weighting adjustment. (B) Forest plot of Logistic Regression results.
X. Lyu: None; P. Gordon: Alexion, 12, Primary investigator at King's college hospital for the NCT04999020 study (ALXN1210-DM-310). No personal payment, Argenx, 12, PI at King's College Hospital for study ARGX-113-2007 and Study ARGX-113-2011, Bristol-Myers Squibb(BMS), 12, POETYK SLE study (NCT05620407), Chief investigator for UK and site PI at King's College Hospital London for this study ., Celltrion Healthcare, 12, Funded to attend EULAR convergence in 2023, Eli Lilly, 12, PI at King's College Hospital for MOJAK, funded by Eli Lilly with University of Manchester as the Sponsor. Termination date aproximate, Galapagos, 1, 2, 12, Chief investigator in UK for Galarisso study (NCT05695950); H. Gunawardena: None; N. McHugh: None; S. Tansley: Boehringer-Ingelheim, 1, 6; A. Prabu: None; P. Lanyon: AstraZeneca, 1, CSL Vifor, 5, 6; J. Miller: None; V. Ong: None; A. Isaacs: None; C. Yee: Amgen, 2; C. Cotton: None; P. Kiely: None; E. Stathopoulou: None; J. Taylor: None; R. Jeffery: None; A. Bharadwaj: None; J. Lilleker: None; J. Lamb: Eli Lilly, 5; h. Chinoy: AstraZeneca, 1, Eli Lilly, 5, Janssen, 1, Pfizer, 1.