Division of Immunology/Rheumatology, Stanford University School of Medicine, Palo Alto, CA, USA
Boehringer Ingelheim Pharmaceuticals, Inc, Ridgefield, CT, USA.
BMJ Open. 2024 Nov 17;14(11):e081687. doi: 10.1136/bmjopen-2023-081687.
This post hoc analysis compared the immunogenicity of the biosimilar adalimumab-adbm (Cyltezo) with the adalimumab reference product (RP; Humira) across indications, including rheumatoid arthritis (RA), Crohn's disease (CD) and plaque psoriasis (PsO), and by patient sex in the VOLTAIRE trials programme.
In each active-comparator randomised controlled trial (RCT), immunogenicity was assessed at various time points by the proportion of patients with antidrug antibodies (ADAs) and neutralising antibodies (nAbs), using acid dissociation followed by electrochemiluminescence assay. Assay sensitivity was 50 ng/mL, and drug tolerance was ≥30 µg/mL (free drug) at the low positive control level.
Minor differences in immunogenicity parameters (ADAs, ADA titres and nAbs) were evident between adalimumab-adbm and adalimumab RP across these three immune-mediated inflammatory diseases (IMIDs). The proportion of ADA-positive and nAb-positive patients increased from baseline over time in all three RCTs, as expected, and was similar in the RA and CD RCTs but with higher numbers of ADA-positive and nAb-positive patients reported in the PsO trial. Subgroup analysis by patient sex showed the same trend.
Differences among the RCTs may partially be explained by concomitant background therapy (methotrexate) in the RA trial, stable doses of azathioprine, 6-mercaptopurine or methotrexate in 36% of patients with CD and absence of background therapy in the PsO RCT. The analyses further confirm the biosimilarity of adalimumab-adbm with the adalimumab RP across IMIDs and provide supporting evidence that adalimumab-adbm is an interchangeable biosimilar with consistent clinical results in patients originally treated with the RP.
VOLTAIRE-RA (NCT02137226; EudraCT 2012-002945-40); VOLTAIRE-CD (NCT02871635; EudraCT 2016-000612-14); VOLTAIRE-PsO (NCT02850965; EudraCT 2016-000613-79).
本事后分析比较了阿达木单抗生物类似药 adalimumab-adbm(Cyltezo)与阿达木单抗参照产品(RP;Humira)在包括类风湿关节炎(RA)、克罗恩病(CD)和斑块状银屑病(PsO)在内的多种适应证以及不同性别患者中的免疫原性。
在每个活性对照随机对照试验(RCT)中,通过采用酸解离后电化学发光测定法检测抗药物抗体(ADA)和中和抗体(nAb)的患者比例,在不同时间点评估免疫原性。检测的灵敏度为 50ng/ml,在低阳性对照水平,药物的最低耐受浓度为≥30μg/ml(游离药物)。
在这三种免疫介导的炎症性疾病(IMIDs)中,adalimumab-adbm 与 adalimumab RP 在免疫原性参数(ADA、ADA 效价和 nAb)方面存在微小差异。在所有三项 RCT 中,ADA 阳性和 nAb 阳性患者的比例随着时间的推移从基线增加,这是预期的,并且在 RA 和 CD RCT 中相似,但在 PsO 试验中报告的 ADA 阳性和 nAb 阳性患者数量更多。按患者性别进行的亚组分析显示出相同的趋势。
RCT 之间的差异部分可能归因于 RA 试验中同时使用了背景治疗(甲氨蝶呤),CD 试验中有 36%的患者稳定剂量使用硫唑嘌呤、6-巯基嘌呤或甲氨蝶呤,而 PsO RCT 中没有使用背景治疗。分析进一步证实了 adalimumab-adbm 与 adalimumab RP 在 IMIDs 方面的生物相似性,并提供了支持证据,表明 adalimumab-adbm 是一种可互换的生物类似物,在最初接受 RP 治疗的患者中具有一致的临床疗效。
VOLTAIRE-RA(NCT02137226;EudraCT 2012-002945-40);VOLTAIRE-CD(NCT02871635;EudraCT 2016-000612-14);VOLTAIRE-PsO(NCT02850965;EudraCT 2016-000613-79)。