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复发性多软骨炎的生物制剂治疗:文献综述。

Biologics in relapsing polychondritis: a literature review.

机构信息

Department of Rheumatology, Henri Mondor Hospital, University Paris XII, Créteil, France.

出版信息

Semin Arthritis Rheum. 2012 Apr;41(5):712-9. doi: 10.1016/j.semarthrit.2011.08.006. Epub 2011 Nov 8.

DOI:10.1016/j.semarthrit.2011.08.006
PMID:22071463
Abstract

BACKGROUND

There is no standardized therapeutic protocol for relapsing polychondritis (RP). Emergence of biologics holds much hope in the management of this connective tissue disease.

OBJECTIVES

To evaluate the efficacy and safety of biologics in patients with active RP.

METHODS

A systematic review of the literature using PubMed was performed through December 2010. MeSH terms and keywords were used relating to RP and biologics. All papers reporting the efficacy and/or safety of biologics in RP were selected. Reference lists of included papers were also searched.

RESULTS

All publications relate to case series or isolated case reports. No randomized controlled trial has been performed. Thirty papers that included 62 patients were published. These patients were treated with TNFα blockers (n = 43), rituximab (n = 11), anakinra (n = 5), tocilizumab (n = 2), and abatacept (n = 1). The endpoint of treatment differs from 1 publication to the other and therefore makes the comparison of efficacy among the various biologics difficult. Biologics were effective in 27 patients, partially effective in 5 patients, and not effective in 29 patients. Safety appeared to be good. However, 4 deaths were recorded (2 sepsis, 1 postoperatively after aortic aneurysm surgery, and 1 after accidental dislocation of the tracheostomy device).

CONCLUSIONS

The experience with biologics in RP is very limited and their real efficacy and indications need to be better defined. Randomized controlled trials, although difficult to perform because of the rarity of RP, are needed to determine the place of biologics in the treatment strategy of this orphan disease.

摘要

背景

对于复发性多软骨炎(RP),目前尚无标准化的治疗方案。生物制剂的出现为这种结缔组织疾病的治疗带来了新的希望。

目的

评估生物制剂治疗活动性 RP 的疗效和安全性。

方法

通过 2010 年 12 月对 PubMed 进行的文献系统回顾,使用了与 RP 和生物制剂相关的 MeSH 术语和关键词。选择所有报告生物制剂治疗 RP 的疗效和/或安全性的论文。还检索了纳入论文的参考文献列表。

结果

所有出版物均涉及病例系列或单独的病例报告。没有进行随机对照试验。发表了 30 篇论文,共纳入 62 例患者。这些患者接受 TNFα 阻滞剂(n=43)、利妥昔单抗(n=11)、阿那白滞素(n=5)、托珠单抗(n=2)和阿巴西普(n=1)治疗。治疗的终点因 1 篇文献而异,因此难以比较各种生物制剂的疗效。生物制剂在 27 例患者中有效,在 5 例患者中部分有效,在 29 例患者中无效。安全性似乎良好。然而,有 4 例死亡记录(2 例脓毒症,1 例主动脉瘤手术后,1 例意外气管切开装置脱位)。

结论

生物制剂治疗 RP 的经验非常有限,其确切疗效和适应证需要进一步明确。由于 RP 的罕见性,进行随机对照试验很困难,但需要这些试验来确定生物制剂在这种罕见疾病治疗策略中的地位。

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