Oral Medicine Unit, Department of Clinic and Preventive Dentistry, Universidade Federal de Pernambuco, Recife, Brazil.
Department of Oral Medicine, University of Pennsylvania School of Dental Medicine, Philadelphia, Pennsylvania.
Oral Dis. 2019 Jun;25 Suppl 1(Suppl 1):102-110. doi: 10.1111/odi.13062.
This systematic review evaluated the efficacy of immunobiologics for the management of oral disease in Sjögren's syndrome (SS).
MEDLINE , Embase, Scopus, and the Cochrane Library were searched for evidence on the use of immunobiologics for management of glandular disease in SS. Primary outcomes were xerostomia and salivary gland dysfunction, assessed via visual analogue scales, disease-specific scales for SS, measurement of salivary flow, ultrasound data, and quality of life measures.
Seventeen studies (11 randomized controlled trials and 6 observational studies) met inclusion criteria. Rituximab showed efficacy in improving salivary gland function but not xerostomia. Abatacept showed promise in improving both xerostomia and salivary flow. Belimumab exhibited long-term improvement of salivary flow and subjective measures. The novel agent CFZ533 improved both disease activity and patient-reported indexes.
There is strong evidence pointing to the efficacy of rituximab in the management of oral disease in SS. Future controlled trials may elucidate the efficacy of belimumab and abatacept. The new drug CFZ533 is a promising alternative for the management of SS and its salivary gland involvement. In considering these agents, the promise of efficacy must be balanced against the harmful effects associated with biologic agents.
本系统评价评估了免疫生物制剂在干燥综合征(SS)口腔疾病管理中的疗效。
检索 MEDLINE、Embase、Scopus 和 Cochrane 图书馆,以获取有关免疫生物制剂治疗 SS 腺体疾病的证据。主要结局指标为口干和唾液腺功能障碍,通过视觉模拟评分、SS 特异性量表、唾液流率测量、超声数据和生活质量测量进行评估。
17 项研究(11 项随机对照试验和 6 项观察性研究)符合纳入标准。利妥昔单抗显示出改善唾液腺功能的疗效,但对口干无影响。阿巴西普在改善口干和唾液流率方面显示出一定的疗效。贝利木单抗显示出长期改善唾液流率和主观指标的效果。新型药物 CFZ533 改善了疾病活动度和患者报告的指标。
有强有力的证据表明利妥昔单抗在 SS 口腔疾病管理中有效。未来的对照试验可能会阐明贝利木单抗和阿巴西普的疗效。新型药物 CFZ533 是治疗 SS 及其唾液腺受累的一种有前途的替代药物。在考虑这些药物时,必须权衡疗效的潜力与生物制剂相关的有害作用。