目的:弥漫性脑桥脑胶质瘤(DIPG)是脑干的侵袭性恶性肿瘤。立体定向活检可以获得分子和遗传信息,用于诊断和潜在的治疗目的。然而,对于活检的安全性或对生存的影响尚无共识.作者旨在描述与DIPG患者相关的神经系统风险以及立体定向活检对生存的影响。
方法:根据PRISMA指南进行系统评价,以确定所有检查接受立体定向活检的DIPG儿科患者的研究。搜索策略部署在PubMed中,Embase,还有Scopus.研究质量是使用建议分级来评估的,评估,开发和评估系统,使用非随机研究-干预工具中的Cochrane偏差风险评估偏倚风险。Bibliographic,人口统计学,临床,结果数据来自符合纳入标准的研究.
结果:在2634篇文章中,包括13个,代表192名接受活检的患者。诊断时的加权平均年龄为7.5岁(范围0.5-17岁)。整体神经外科并发症发生率为13.02%(25/192)。最常见的神经外科并发症是颅神经麻痹(4.2%,8/192),其中颅神经VII最常见(37.5%,3/8)。第二常见的并发症是围手术期出血(3.6%,7/192),其次是偏瘫(2.1%,4/192),言语障碍(1.6%,3/192),例如构音障碍和言语障碍,和运动障碍(1.0%,2/192)。脑积水较不常见(0.5%,1/192),并且没有与伤口感染/裂开有关的并发症(0%,0/192)或CSF泄漏(0%,0/192)。没有明确的死亡率归因于活检。活检的诊断率显示加权平均值为97.4%(范围91%-100%)。在报告生存数据的研究中,37.6%(32/85)的患者在研究随访期内(范围2周-48个月)死亡。活检患者的平均总生存期为9.73个月(SD0.68,中位数为10个月,6-13个月)。
结论:接受活检的DIPG患儿有轻度至中度的神经外科并发症发生率,且无过度的发病率。具有合理可接受的手术风险和高诊断率,DIPGs的立体定向活检可以对可能影响预后和未来治疗策略发展的患者特异性分子和遗传特征进行表征.
Diffuse intrinsic pontine gliomas (DIPGs) are aggressive and malignant tumors of the brainstem. Stereotactic biopsy can obtain molecular and genetic information for diagnostic and potentially therapeutic purposes. However, there is no consensus on the safety of biopsy or effect on survival. The authors aimed to characterize neurological risk associated with and the effect of stereotactic biopsy on survival among patients with DIPGs.
A systematic
review was performed in accordance with PRISMA guidelines to identify all studies examining pediatric patients with DIPG who underwent stereotactic biopsy. The search strategy was deployed in PubMed, Embase, and Scopus. The quality of studies was assessed using the Grading of Recommendations, Assessment, Development and Evaluation system, and risk of bias was evaluated with the Cochrane Risk of Bias in Nonrandomized Studies-of Interventions tool. Bibliographic, demographic, clinical, and outcome data were extracted from studies meeting inclusion criteria.
Of 2634 resultant articles, 13 were included, representing 192 patients undergoing biopsy. The weighted mean age at diagnosis was 7.5 years (range 0.5-17 years). There was an overall neurosurgical complication rate of 13.02% (25/192). The most common neurosurgical complication was cranial nerve palsy (4.2%, 8/192), of which cranial nerve VII was the most common (37.5%, 3/8). The second most common complication was perioperative hemorrhage (3.6%, 7/192), followed by hemiparesis (2.1%, 4/192), speech disorders (1.6%, 3/192) such as dysarthria and dysphasia, and movement disorders (1.0%, 2/192). Hydrocephalus was less commonly reported (0.5%, 1/192), and there were no complications relating to wound infection/dehiscence (0%, 0/192) or CSF leak (0%, 0/192). No mortality was specifically attributed to biopsy. Diagnostic yield of biopsy revealed a weighted mean of 97.4% (range 91%-100%). Of the studies reporting survival data, 37.6% (32/85) of patients died within the study follow-up period (range 2 weeks-48 months). The mean overall survival in patients undergoing biopsy was 9.73 months (SD 0.68, median 10 months, range 6-13 months).
Children with DIPGs undergoing biopsy have mild to moderate rates of neurosurgical complications and no excessive morbidity. With reasonably acceptable surgical risk and high diagnostic yield, stereotactic biopsy of DIPGs can allow for characterization of patient-specific molecular and genetic features that may influence prognosis and the development of future therapeutic strategies.