Pediatric Rare Diseases Unit, Department of Pediatrics, MBBM Foundation, ATS Monza e Brianza, Via Pergolesi 33, 20900, Monza, Italy.
Centre of Biostatistics for Clinical Epidemiology, School of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Orphanet J Rare Dis. 2018 Feb 8;13(1):32. doi: 10.1186/s13023-018-0771-0.
Enzyme replacement therapy (ERT) has deeply modified the clinical history of Infantile Onset Pompe Disease (IOPD). However, its long-term effectiveness is still not completely defined. Available data shows a close relationship between clinical outcome and patients' cross-reactive immunological status (CRIM), being CRIM-negative status a negative prognostic factor. At the same time limited data are available on the long-term treatment in CRIM-positive infants.
A retrospective multicentre observational study was designed to analyse the long-term effectiveness of ERT in IOPD. Thirteen Italian centres spread throughout the country were involved and a cohort of 28 patients (15 females, 13 males, born in the period: February 2002-January 2013) was enrolled. IOPD diagnosis was based on clinical symptoms, enzymatic and molecular analysis. All patients received ERT within the first year of life. Clinical, laboratory, and functional data (motor, cardiac and respiratory) were collected and followed for a median period of 71 months (5 years 11 months).
Median age at onset, diagnosis and start of ERT were 2, 3 and 4 months, respectively. CRIM status was available for 24/28 patients: 17/24 (71%) were CRIM-positive. Nineteen patients (67%) survived > 2 years: 4 were CRIM-negative, 14 CRIM-positive and one unknown. Six patients (5 CRIM-positive and one unknown) never needed ventilation support (21,4%) and seven (6 CRIM-positive and one unknown: 25%) developed independent ambulation although one subsequently lost this function. Brain imaging study was performed in 6 patients and showed peri-ventricular white matter abnormalities in all of them. Clinical follow-up confirmed the better prognosis for CRIM-positive patients, though a slow, progressive worsening of motor and/or respiratory functions was detected in 8 patients.
These data are the result of the longest independent retrospective study on ERT in IOPD reported so far outside clinical trials. The data obtained confirmed the better outcome of the CRIM-positive patients but at the same time, showed the inability of the current therapeutic approach to reverse or stabilize the disease progression. The results also evidenced the involvement of central nervous system in Pompe disease. To better understand the disease clinical history and to improve treatment efficacy larger multicentre studies are needed as well as the development of new therapeutic approaches.
酶替代疗法(ERT)极大地改变了婴儿期发作庞贝病(IOPD)的临床病史。然而,其长期疗效仍不完全明确。现有数据表明,临床结局与患者的交叉反应免疫状态(CRIM)密切相关,CRIM 阴性是一个负面的预后因素。同时,关于 CRIM 阳性婴儿的长期治疗,可用的数据有限。
设计了一项回顾性多中心观察性研究,以分析 IOPD 中 ERT 的长期疗效。涉及了意大利 13 个分布在全国各地的中心,并招募了 28 名患者(15 名女性,13 名男性,出生于 2002 年 2 月至 2013 年 1 月)。IOPD 的诊断基于临床症状、酶学和分子分析。所有患者在出生后的第一年都接受了 ERT。收集了临床、实验室和功能数据(运动、心脏和呼吸),并进行了中位时间为 71 个月(5 年 11 个月)的随访。
发病、诊断和开始 ERT 的中位年龄分别为 2、3 和 4 个月。24/28 名患者的 CRIM 状态可用:17/24(71%)为 CRIM 阳性。19 名患者(67%)存活时间>2 年:4 名 CRIM 阴性,14 名 CRIM 阳性,1 名未知。6 名患者(5 名 CRIM 阳性和 1 名未知:21.4%)从未需要通气支持,7 名患者(6 名 CRIM 阳性和 1 名未知:25%)独立行走,尽管其中 1 名随后失去了这项功能。对 6 名患者进行了脑部影像学研究,结果显示他们均存在脑室周围白质异常。临床随访证实了 CRIM 阳性患者的预后较好,但同时发现 8 名患者的运动和/或呼吸功能呈缓慢、进行性恶化。
这些数据是迄今为止在临床试验之外报告的关于 IOPD 中 ERT 的最长的独立回顾性研究的结果。获得的数据证实了 CRIM 阳性患者的更好结局,但同时表明,目前的治疗方法无法逆转或稳定疾病进展。结果还表明中枢神经系统也参与了庞贝病。为了更好地了解疾病的临床病史并提高治疗效果,需要进行更大规模的多中心研究,并开发新的治疗方法。