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Therapeutic approach to IgG4-related disease: A systematic review

机译:IgG4相关疾病的治疗方法:系统评价

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To review the reported evidence on the therapeutic management of IgG4-related disease (IgG4-RD) in clinical practice.A systematic search of the literature was conducted. The primary outcome measured was the rate of efficacy of first-line therapeutic approaches. Secondary outcomes measured included the rate of disease relapse, the outcome of untreated patients, the rate of patients without drug therapy at the end of follow-up, the rate of side effects, and mortality. The MOOSE, AHRQ, STROBE, and GRACE recommendations/statements were followed.The results of the systematic search strategy yielded 62 studies that included a total of 3034 patients. Complete information about first-line therapeutic regimens was detailed in 1952 patients, including glucocorticoid-based regimens in 1437 (74%), drug-free regimens in 213 (11%), and other therapies in 38 (2%). No therapy (wait and see management) was reported in 264 (13%) patients. The efficacy of monotherapy with glucocorticoids was specified in 1220 patients, of whom 97% had a therapeutic response. Relapses, however, were reported in 464/1395 (33%) patients despite typically short follow-up periods. Therapeutic efficacy was reported in 219/231 (95%) of relapses treated with glucocorticoids, 56/69 (81%) of those treated with azathioprine, 16/22 (72%) of those treated with other immunosuppressive agents, and in the 9 cases treated with rituximab (100%). In 14 studies, the authors detailed the outcome of 159/246 patients with wait-and-see management; spontaneous improvement or resolution was reported in 68 (43%) cases. Wide heterogeneity was observed with respect to the first-line therapeutic approaches used for the different organ-specific disease subsets, including significant differences in the mean dose of glucocorticoids used.Nearly 70% of reported IgG4-RD patients are treated with oral glucocorticoids in monotherapy. However, the therapeutic management is heavily influenced by geographical, epidemiological, and clinical factors, especially with respect to the predominant organ affected. The frequency of glucocorticoid failure to induce sustained remissions both during and after treatment and the assessment of glucocorticoid toxicity in IgG4-RD require further study.
机译:在临床实践中回顾有关IgG4相关疾病(IgG4-RD)的治疗管理的报道证据。进行了系统的文献检索。衡量的主要结果是一线治疗方法的功效率。测量的次要结局包括疾病复发率,未治疗患者的结局,随访结束时未接受药物治疗的患者率,副作用发生率和死亡率。遵循了MOOSE,AHRQ,STROBE和GRACE的建议/声明。系统搜索策略的结果产生了62项研究,包括3034例患者。关于一线治疗方案的完整信息在1952名患者中得到了详细介绍,包括1437例(74%)基于糖皮质激素的方案,213例(11%)的无药物方案以及38例(2%)的其他疗法。 264名(13%)患者未报告治疗方法(等待治疗)。在1220例患者中明确了糖皮质激素单一疗法的疗效,其中97%的患者有治疗反应。然而,尽管随访时间通常较短,但仍有464/1395例患者(33%)复发。糖皮质激素治疗的复发率为219/231(95%),硫唑嘌呤治疗的复发率为56/69(81%),其他免疫抑制剂治疗的复发率为16/22(72%),利妥昔单抗治疗的病例(100%)。在14项研究中,作者详细介绍了159/246例接受观望治疗的患者的预后。 68例(43%)病例报告有自发性改善或消退。在针对不同器官特异性疾病亚群的一线治疗方法中观察到广泛的异质性,包括所用糖皮质激素的平均剂量存在显着差异。近70%的报道的IgG4-RD患者在单一疗法中使用口服糖皮质激素治疗。但是,治疗管理受到地理,流行病学和临床因素的严重影响,尤其是在受影响的主要器官方面。糖皮质激素治疗期间和治疗后诱导持续缓解的失败频率以及对IgG4-RD中糖皮质激素毒性的评估尚需进一步研究。

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