Cohen Hillel P, Bodenmueller Wolfram
Scientific Affairs, Sandoz Inc., 100 College Road West, Princeton, NJ, 08540, USA.
Sandoz Deutschland/Hexal AG, Holzkirchen, Germany.
BioDrugs. 2024 May;38(3):331-339. doi: 10.1007/s40259-024-00655-4. Epub 2024 Mar 23.
As of 31 December, 2023, 31 observational studies have been published, including a total of 6081 patients who underwent a switch from one biosimilar to another biosimilar of the same reference biologic. Most studies evaluated infliximab, while a smaller number evaluated adalimumab, rituximab or etanercept. Indications studied now include sarcoidosis, as well as the indications previously reported of rheumatoid arthritis, psoriatic arthritis, axial spondyloarthritis/ankylosing spondylitis and inflammatory bowel disease (Crohn's disease and ulcerative colitis). This updated data set includes eight additional studies and 2386 more patients compared with those included in an earlier systematic review of biosimilar-to-biosimilar switching. In addition, since the earlier systematic review was published in 2022, the European Medicines Agency has stated that reference-to-biosimilar and biosimilar-to-biosimilar switching in the European Union is safe and efficacy remains unchanged after switching. Furthermore, following a review of the available evidence, the US Food and Drug Administration has confirmed that initial safety and immunogenicity concerns related to biosimilar switching are unfounded and that no differences are observed in efficacy, safety or immunogenicity following one or more switches. The availability of this new efficacy and safety data together with the supportive statements from the European Medicines Agency and the Food and Drug Administration re-confirm the conclusion that as a scientific matter, biosimilar-to-biosimilar switching is an effective clinical practice, with no new safety concerns. Any suggestions to the contrary are not supported by the evidence.
截至2023年12月31日,已发表31项观察性研究,共纳入6081例从一种生物类似药转换为同一种参照生物药的另一种生物类似药的患者。大多数研究评估了英夫利昔单抗,少数研究评估了阿达木单抗、利妥昔单抗或依那西普。目前研究的适应症包括结节病,以及先前报道的类风湿性关节炎、银屑病关节炎、中轴型脊柱关节炎/强直性脊柱炎和炎症性肠病(克罗恩病和溃疡性结肠炎)。与早期关于生物类似药间转换的系统评价相比,这个更新的数据集增加了8项研究和2386例患者。此外,自早期系统评价于2022年发表以来,欧洲药品管理局表示,在欧盟,参照生物药转换为生物类似药以及生物类似药间的转换是安全的,转换后疗效保持不变。此外,在对现有证据进行审查后,美国食品药品监督管理局确认,最初对生物类似药转换的安全性和免疫原性担忧是没有根据的,在一次或多次转换后,疗效、安全性或免疫原性方面未观察到差异。这些新的疗效和安全性数据的可得性,以及欧洲药品管理局和美国食品药品监督管理局的支持性声明,再次证实了这样一个结论:从科学角度来看,生物类似药间的转换是一种有效的临床实践,不存在新的安全问题。任何相反的建议都没有证据支持。