Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.
Department of Gastroenterology, Akershus University Hospital, Lørenskog, Norway.
JAMA. 2021 Dec 21;326(23):2375-2384. doi: 10.1001/jama.2021.21316.
Proactive therapeutic drug monitoring (TDM), consisting of individualized treatment based on scheduled assessments of serum drug levels, has been proposed as an alternative to standard therapy to optimize efficacy and safety of infliximab and other biologic drugs. However, it remains unclear whether proactive TDM improves clinical outcomes during maintenance therapy.
To assess whether proactive TDM during maintenance therapy with infliximab improves treatment efficacy by preventing disease worsening compared with standard infliximab therapy without TDM.
DESIGN, SETTING, AND PARTICIPANTS: Randomized, parallel-group, open-label clinical trial including 458 adults with rheumatoid arthritis, spondyloarthritis, psoriatic arthritis, ulcerative colitis, Crohn disease, or psoriasis undergoing maintenance therapy with infliximab in 20 Norwegian hospitals. Patients were recruited from June 7, 2017, to December 12, 2019. Final follow-up took place on December 14, 2020.
Patients were randomized 1:1 to proactive TDM with dose and interval adjustments based on scheduled monitoring of serum drug levels and antidrug antibodies (TDM group; n = 228) or to standard infliximab therapy without drug and antibody level monitoring (standard therapy group; n = 230).
The primary outcome was sustained disease control without disease worsening, defined by disease-specific composite scores or consensus about disease worsening between patient and physician leading to a major change in treatment (switching to another biologic drug, adding an immunosuppressive drug including glucocorticoids, or increasing the infliximab dose), during the 52-week study period.
Among 458 randomized patients (mean age, 44.8 [SD, 14.3] years; 216 women [49.8%]), 454 received their randomly allocated intervention and were included in the full analysis set. The primary outcome of sustained disease control without disease worsening was observed in 167 patients (73.6%) in the TDM group and 127 patients (55.9%) in the standard therapy group. The estimated adjusted difference was 17.6% (95% CI, 9.0%-26.2%; P < .001) favoring TDM. Adverse events were reported in 137 patients (60%) and 142 patients (63%) in the TDM and standard therapy groups, respectively.
Among patients with immune-mediated inflammatory diseases undergoing maintenance therapy with infliximab, proactive TDM was more effective than treatment without TDM in sustaining disease control without disease worsening. Further research is needed to compare proactive TDM with reactive TDM, to assess the effects on long-term disease complications, and to evaluate the cost-effectiveness of this approach.
ClinicalTrials.gov Identifier: NCT03074656.
主动的治疗药物监测(TDM),由根据血清药物水平的预定评估制定的个体化治疗组成,已被提议作为优化英夫利昔单抗和其他生物药物疗效和安全性的标准治疗的替代方法。然而,主动 TDM 是否能在维持治疗期间改善临床结果仍不清楚。
评估在英夫利昔单抗维持治疗期间,主动 TDM 是否通过预防疾病恶化而优于没有 TDM 的标准英夫利昔单抗治疗,从而提高治疗效果。
设计、地点和参与者:这是一项包括 458 名成年人的随机、平行组、开放标签临床试验,他们在挪威 20 家医院接受英夫利昔单抗维持治疗,患有类风湿关节炎、脊柱关节炎、银屑病关节炎、溃疡性结肠炎、克罗恩病或银屑病。患者于 2017 年 6 月 7 日至 2019 年 12 月 12 日招募,最终随访于 2020 年 12 月 14 日进行。
患者被随机分为 1:1 组,分别接受主动 TDM 治疗,根据预定监测血清药物水平和抗药物抗体进行剂量和间隔调整(TDM 组;n=228)或接受无药物和抗体水平监测的标准英夫利昔单抗治疗(标准治疗组;n=230)。
主要结局是在 52 周的研究期间,没有疾病恶化的持续疾病控制,定义为特定疾病的综合评分或患者和医生之间关于疾病恶化的共识导致治疗的重大改变(改用另一种生物药物、添加免疫抑制剂包括糖皮质激素,或增加英夫利昔单抗剂量)。
在 458 名随机患者(平均年龄,44.8[SD,14.3]岁;216 名女性[49.8%])中,454 名接受了随机分配的干预措施,并纳入了全分析集。在 TDM 组中,167 名(73.6%)患者和标准治疗组中 127 名(55.9%)患者观察到持续疾病控制而没有疾病恶化。估计调整后的差异为 17.6%(95%CI,9.0%-26.2%;P<0.001),有利于 TDM。在 TDM 组和标准治疗组中,分别有 137 名(60%)和 142 名(63%)患者报告了不良事件。
在接受英夫利昔单抗维持治疗的免疫介导性炎症性疾病患者中,主动 TDM 比不进行 TDM 治疗更能有效地维持疾病控制而不恶化。需要进一步研究来比较主动 TDM 与反应性 TDM,评估对长期疾病并发症的影响,并评估这种方法的成本效益。
ClinicalTrials.gov 标识符:NCT03074656。