Verazza Sara, Davì Sergio, Consolaro Alessandro, Bovis Francesca, Insalaco Antonella, Magni-Manzoni Silvia, Nicolai Rebecca, Marafon Denise Pires, De Benedetti Fabrizio, Gerloni Valeria, Pontikaki Irene, Rovelli Francesca, Cimaz Rolando, Marino Achille, Zulian Francesco, Martini Giorgia, Pastore Serena, Sandrin Chiara, Corona Fabrizia, Torcoletti Marta, Conti Giovanni, Fede Claudia, Barone Patrizia, Cattalini Marco, Cortis Elisabetta, Breda Luciana, Olivieri Alma Nunzia, Civino Adele, Podda Rosanna, Rigante Donato, La Torre Francesco, D'Angelo Gianfranco, Jorini Mauro, Gallizzi Romina, Maggio Maria Cristina, Consolini Rita, De Fanti Alessandro, Muratore Valentina, Alpigiani Maria Giannina, Ruperto Nicolino, Martini Alberto, Ravelli Angelo
Università degli Studi di Genova, Genova, Italy.
Istituto Giannina Gaslini, Genova, Italy.
Pediatr Rheumatol Online J. 2016 Dec 20;14(1):68. doi: 10.1186/s12969-016-0126-0.
Data from routine clinical practice are needed to further define the efficacy and safety of biologic medications in children with juvenile idiopathic arthritis (JIA). The aim of this analysis was to investigate the disease status, reasons for discontinuation and adverse events in Italian JIA patients treated with etanercept (ETN).
In 2013, all centers of the Italian Pediatric Rheumatology Study Group were asked to make a census of patients given ETN after January 2000. Patients were classified in three groups: group 1 = patients still taking ETN; group 2 = patients discontinued from ETN for any reasons; group 3 = patients lost to follow-up while receiving ETN. All three groups received a retrospective assessment; patients in group 1 also underwent a cross-sectional assessment.
1038 patients were enrolled by 23 centers: 422 (40.7%) were in group 1, 462 (44.5%) in group 2, and 154 (14.8%) in group 3. Median duration of ETN therapy was 2.5 years. At cross-sectional assessment, 41.8% to 48.6% of patients in group 1 met formal criteria for inactive disease, whereas 52.4% of patients in group 2 and 55.8% of patients in group 3 were judged in clinical remission by their caring physician at last visit. A relatively greater proportion of patients with systemic arthritis were discontinued or lost to follow-up. Parent evaluations at cross-sectional visit in group 1 showed that 52.4% of patients had normal physical function, very few had impairment in quality of life, 51.2% had no pain, 76% had no morning stiffness, and 82.7% of parents were satisfied with their child's illness outcome. Clinically significant adverse events were reported for 27.8% of patients and ETN was discontinued for side effects in 9.5%. The most common adverse events were new onset or recurrent uveitis (10.2%), infections (6.6%), injection site reactions (4.4%), and neuropsychiatric (3.1%), gastrointestinal (2.4%), and hematological disorders (2.1%). Ten patients developed an inflammatory bowel disease and 2 had a malignancy. One patient died of a fulminant streptococcal sepsis.
Around half of the patients achieved complete disease quiescence under treatment with ETN. The medication was overall well tolerated, as only one quarter of patients experienced clinically significant adverse events and less than 10% had treatment discontinued for toxicity.
需要来自常规临床实践的数据来进一步明确生物制剂在幼年特发性关节炎(JIA)患儿中的疗效和安全性。本分析的目的是调查接受依那西普(ETN)治疗的意大利JIA患者的疾病状况、停药原因及不良事件。
2013年,意大利儿科风湿病研究组的所有中心被要求对2000年1月后接受ETN治疗的患者进行普查。患者分为三组:第1组=仍在服用ETN的患者;第2组=因任何原因停用ETN的患者;第3组=接受ETN治疗期间失访的患者。对所有三组进行回顾性评估;第1组的患者还接受了横断面评估。
23个中心共纳入1038例患者:第1组422例(40.7%),第2组462例(44.5%),第3组154例(14.8%)。ETN治疗的中位持续时间为2.5年。在横断面评估中,第1组41.8%至48.6%的患者符合疾病无活动的正式标准,而第2组52.4%的患者和第3组55.8%的患者在最后一次就诊时被其主治医生判定为临床缓解。全身型关节炎患者中停药或失访的比例相对较高。第1组横断面访视时家长评估显示,52.4%的患者身体功能正常,很少有生活质量受损,51.2%的患者无疼痛,76%的患者无晨僵,82.7%的家长对孩子的疾病结局满意。27.8%的患者报告了具有临床意义的不良事件,9.5%的患者因副作用停用ETN。最常见的不良事件是新发或复发性葡萄膜炎(10.2%)、感染(6.6%)、注射部位反应(4.4%)以及神经精神疾病(3.1%)、胃肠道疾病(2.4%)和血液系统疾病(2.1%)。10例患者发生炎症性肠病,2例患恶性肿瘤。1例患者死于暴发性链球菌败血症。
约一半的患者在ETN治疗下实现了疾病完全缓解。该药物总体耐受性良好,因为只有四分之一的患者经历了具有临床意义的不良事件,不到10%的患者因毒性停药。