Department of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Ministry of Science & Technology, State Key Laboratory of Complex Severe and Rare Diseases, Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, Beijing, China.
Department of Hematology, Chinese Academy of Medical Sciences & Peking Union Medical College Hospital, Beijing, China.
Clin Exp Med. 2023 Dec;23(8):5433-5443. doi: 10.1007/s10238-023-01248-1. Epub 2023 Nov 6.
Thrombocytopenia is a common manifestation associated with the presence of antiphospholipid antibodies (aPL). The aim of this study is to investigate the efficacy and safety of tacrolimus treatment in aPL associated thrombocytopenia. This is a single-center retrospective study. Patients who had persistent positive aPL and thrombocytopenia that was treated with tacrolimus were included. A total of 49 patients [38 females (77.6%)] were enrolled from Nov 2013 to Apr 2022 with a median treatment duration of 22 months. Seventeen fulfilled classification criteria of antiphospholipid syndrome (APS), 18 systemic lupus erythematosus (SLE). The median age of study patients was 37 years (IQR 31, 48). Forty-three (87.8%) patients were on concomitant use of glucocorticoids, 6 on tacrolimus monotherapy. The overall response rate in this cohort was 85.7% (n = 42), including 49% of complete responses (n = 24). The median time to achieve a response was 3 months. Nine (18.4%) patients with overall response experienced a loss of response. The response rate during follow-up in patients with monotherapy was noninferior. Patients with positive antinuclear antibody (ANA) showed the tendency of maintaining response (p = 0.028). The 19 patients who were on medium and high dosage of glucocorticoids (> 15 mg prednisone/d) managed to taper glucocorticoids rapidly. Side effects were reported in 12.2% (n = 6) of the patients (elevated creatinine, general malaise, elevated liver enzyme). Tacrolimus has adequate efficacy, steroid-sparing effect and is well tolerated for aPL associated thrombocytopenia. Patients with positive ANA might benefit the most from tacrolimus treatment.
血小板减少症是一种常见的与抗磷脂抗体 (aPL) 相关的表现。本研究旨在探讨他克莫司治疗 aPL 相关血小板减少症的疗效和安全性。这是一项单中心回顾性研究。纳入了接受他克莫司治疗且持续存在阳性 aPL 和血小板减少症的患者。共有 49 名患者[38 名女性 (77.6%)]于 2013 年 11 月至 2022 年 4 月入组,中位治疗时间为 22 个月。17 名患者符合抗磷脂综合征 (APS) 的分类标准,18 名系统性红斑狼疮 (SLE)。研究患者的中位年龄为 37 岁 (IQR 31, 48)。43 (87.8%)名患者同时使用糖皮质激素,6 名患者接受他克莫司单药治疗。该队列的总体缓解率为 85.7% (n = 42),包括 49%的完全缓解 (n = 24)。达到缓解的中位时间为 3 个月。9 (18.4%)名总体缓解患者出现缓解丧失。单药治疗患者在随访期间的缓解率无差异。抗核抗体 (ANA) 阳性的患者有维持缓解的趋势 (p = 0.028)。接受中高剂量糖皮质激素 (> 15 mg 泼尼松/天) 的 19 名患者能够快速减少糖皮质激素的剂量。有 12.2% (n = 6)的患者报告了副作用 (肌酐升高、全身不适、肝酶升高)。他克莫司治疗 aPL 相关血小板减少症具有足够的疗效、减少激素用量的作用,且耐受性良好。ANA 阳性的患者可能从他克莫司治疗中获益最大。