医学
内科学
免疫抑制
队列
回顾性队列研究
联合疗法
队列研究
全身疗法
前瞻性队列研究
红斑狼疮
强的松
免疫病理学
结缔组织病
狼疮性肾炎
完全响应
羟基氯喹
免疫学
自身免疫性疾病
维持疗法
贝里穆马布
不利影响
外科
系统性红斑狼疮
胃肠病学
化疗
作者
Yiduo Sun,Yuting Wang,Heng Cao,Yini Ke,Weiqian Chen,Chris Wincup,Jin Lin
标识
DOI:10.1093/rheumatology/keag535
摘要
OBJECTIVES: To compare B-cell-targeted therapy with conventional glucocorticoid-based immunosuppression in first-episode systemic lupus erythematosus (SLE)-associated warm autoimmune haemolytic anaemia (AIHA). METHODS: We conducted a multicampus retrospective cohort study from 1 March 2020 to 1 February 2026. Eligible patients had SLE-associated warm AIHA, baseline haemoglobin <90 g/L and laboratory evidence of haemolysis. Treatment exposure was classified within 14 days of treatment initiation: conventional therapy or B-cell-targeted therapy with rituximab, belimumab or telitacicept. The primary outcome was 6-month overall response rate (ORR; complete or partial response). RESULTS: Of 246 SLE hospitalisation records screened, 70 patients were included; 27 received conventional therapy and 43 received B-cell-targeted therapy. The B-cell-targeted therapy group was younger and had higher baseline SLEDAI-2K scores. Six-month ORR was 89.7% with B-cell-targeted therapy and 85.7% with conventional therapy (OR 1.45, 95% CI 0.19-9.61; P = 0.687), with corresponding complete response rates of 61.5% and 42.9%. At 1 month, prednisone-equivalent dose was lower with B-cell-targeted therapy (40.0 vs 50.0 mg/day; P = 0.023). Twelve-month ORR was 89.3% with B-cell-targeted therapy and 73.7% with conventional therapy, and relapse-free survival did not differ significantly. Within 6 months, 13 inpatient-recorded adverse-event episodes, including fatal events, were documented. In telitacicept-treated patients (n = 7), all evaluable patients achieved ORR at 1, 3 and 6 months. CONCLUSIONS: Six- and 12-month ORR did not differ significantly between treatment strategies. The numerically higher complete response rate, more stable 12-month response and earlier glucocorticoid reduction with B-cell-targeted therapy, together with the telitacicept findings, are exploratory and require prospective validation.
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