Mount Sinai School of Medicine, Tisch Cancer Institute, New York, NY, USA.
Int J Hematol. 2022 Dec;116(6):947-955. doi: 10.1007/s12185-022-03430-9. Epub 2022 Aug 10.
Anti-cytokine therapies have been gaining attention as a means of improving outcomes in adult secondary HLH (asHLH), which currently has poor outcomes when treated with standard etoposide-based therapies. Anakinra is an interleukin-1 antagonist that is increasingly being used in the management of asHLH. Here is described a multi-hospital series of 16 adult patients with secondary HLH treated with anakinra. Provoking factors of secondary HLH included hematologic malignancy (n = 7, 44%), bacterial infection (n = 7, 44%), viral infection (n = 5, 31%), rheumatologic disorder (n = 4, 25%), and unknown (n = 1, 6%). Five patients remained alive at time of last follow-up (OS = 31%). Median OS was 1.7 months from initiation of anakinra (range 0.2-59). OS among patients with rheumatologic causes of secondary HLH was 75%, whereas only 17% of patients with other provoking factors survived (p = 0.0293). Anakinra was well tolerated, with only 1 patient experiencing associated toxicity (grade 3 liver injury). Anakinra may be useful in the management of asHLH provoked by rheumatologic conditions, although its benefit in asHLH provoked by other factors may be limited.
抗细胞因子疗法作为改善成人继发性噬血细胞性淋巴组织细胞增生症(sHLH)预后的一种手段受到关注,目前该病采用标准依托泊苷为基础的治疗方法预后较差。阿那白滞素是一种白细胞介素-1 拮抗剂,越来越多地用于 sHLH 的治疗。本研究描述了 16 例接受阿那白滞素治疗的继发性 HLH 成年患者的多中心系列研究。继发性 HLH 的诱发因素包括血液恶性肿瘤(n=7,44%)、细菌感染(n=7,44%)、病毒感染(n=5,31%)、风湿性疾病(n=4,25%)和原因不明(n=1,6%)。5 例患者在最后一次随访时仍存活(OS=31%)。从开始使用阿那白滞素到中位 OS 的时间为 1.7 个月(范围 0.2-59)。继发于风湿性疾病的 sHLH 患者的 OS 为 75%,而其他诱因患者的存活率仅为 17%(p=0.0293)。阿那白滞素耐受性良好,仅有 1 例患者出现相关毒性(3 级肝损伤)。阿那白滞素可能对风湿性疾病引起的 sHLH 治疗有用,但其在其他因素引起的 sHLH 中的获益可能有限。