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延长银屑病关节炎患者生物制剂给药间隔时间:一项单中心回顾性研究。

Lengthening the time intervals between doses of biological agents in psoriatic arthritis patients: A single-center retrospective study.

作者信息

Lorenzin Mariagrazia, Ortolan Augusta, de Hooge Manouk, Frallonardo Paola, Piccoli Antonio, Cozzi Franco, Oliviero Francesca, Punzi Leonardo, Ramonda Roberta

机构信息

Rheumatology Unit, Department of Medicine DIMED-University of Padova, Padova, Italy.

Nephrology Unit, Department of Medicine DIMED-University of Padova, Padova, Italy.

出版信息

Int J Immunopathol Pharmacol. 2015 Dec;28(4):479-87. doi: 10.1177/0394632015599446. Epub 2015 Sep 17.

Abstract

Anti-tumor necrosis factor (TNF) alpha therapy has changed the course of psoriatic arthritis (PsA), but clinical experience about lengthening of time intervals between drug administrations is still limited. The aims of the study were to evaluate: (1) the long-term efficacy (over a 4-year period) of etanercept/adalimumab in a subset of PsA patients who did not require switches; and (2) the progressive lengthening of time intervals between treatments in patients who achieved minimal disease activity (MDA). PsA outpatients attending the Rheumatology Clinic-University of Padova who took a single anti-TNF agent (etanercept/adalimumab) for a 4-year period were studied. Therapy efficacy was assessed using clinical, biochemical, and disease activity (DA) indexes. The intervals between treatments were empirically and progressively lengthened after MDA was reached and maintained. One hundred and forty-one patients (mean age, 51.22 ± 12.34 years; mean disease duration, 12.1 ± 8.42 years) treated with etanercept/adalimumab (47.5% and 52.5%, respectively) were studied. DA indexes showed a marked, persistent improvement in all the patients throughout 4 years. The interval between injections could be extended in 46.1% of the patients (35% for adalimumab, 58% for etanercept) without provoking relapses. The mean therapy interval at the end of the study period was 3.12 weeks for adalimumab 40 mg (with respect to 2 weeks) and 2.75 weeks for etanercept 25 mg (with respect to 0.5 weeks). The new therapy timetable also led to cost savings. In conclusion, lengthening the time intervals between injections of anti-TNF agents in PsA patients who reach MDA is safe, effective, cost-effective, and facilitates patient compliance.

摘要

抗肿瘤坏死因子(TNF)α治疗改变了银屑病关节炎(PsA)的病程,但关于延长药物给药时间间隔的临床经验仍然有限。本研究的目的是评估:(1)在一组不需要换药的PsA患者中,依那西普/阿达木单抗的长期疗效(超过4年);(2)达到最小疾病活动度(MDA)的患者治疗时间间隔的逐步延长。对帕多瓦大学风湿病诊所的PsA门诊患者进行了研究,这些患者接受单一抗TNF药物(依那西普/阿达木单抗)治疗达4年。使用临床、生化和疾病活动(DA)指标评估治疗效果。在达到并维持MDA后,根据经验逐步延长治疗间隔。研究了141例接受依那西普/阿达木单抗治疗的患者(分别为47.5%和52.5%),平均年龄为51.22±12.34岁,平均病程为12.1±8.42年。DA指标显示所有患者在4年中均有显著且持续的改善。46.1%的患者(阿达木单抗为35%,依那西普为58%)可以延长注射间隔而不引发复发。在研究期末,阿达木单抗40mg的平均治疗间隔为3.12周(相对于2周),依那西普25mg的平均治疗间隔为2.75周(相对于0.5周)。新的治疗时间表还节省了成本。总之,对于达到MDA的PsA患者,延长抗TNF药物的注射时间间隔是安全、有效、具有成本效益的,并且有助于患者依从性。

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