Pietschmann Sophie, von Bueren André O, Kerber Michael J, Baumert Brigitta G, Kortmann Rolf Dieter, Müller Klaus
Department of Radiation-Oncology, University Medical Center Leipzig, Leipzig, Saxony, Germany.
Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, University Medical Center Goettingen, Goettingen, Lower Saxony, Germany.
PLoS One. 2015 Apr 10;10(4):e0121592. doi: 10.1371/journal.pone.0121592. eCollection 2015.
To determine the characteristics, treatments and outcomes of patients with glioblastoma multiforme (GBM) or gliosarcoma (GS) and metastases outside of the central nervous system (CNS).
PubMed and Web of Science searches for peer-reviewed articles pertaining to GBM/ GS patients with metastatic dissemination were conducted using the keywords gliosarcoma, glioblastoma, GBM, metastasis, metastases and metastatic. Additionally, we performed hand search following the references from the selected papers. Cases with metastases to the CNS were excluded and evaluated in a separate study.
109 articles published between 1928 and 2013 were eligible. They reported on 150 patients. We observed a remarkable increase in the number of cases per decade over time. Median overall survival from diagnosis of metastasis (OSM+) was 6.0 ± 0.8 months and median overall survival from initial diagnosis (OSID) 13 ± 2.4 months. On univariate analyses, gender, age, the histological subtype, the time interval between initial diagnosis and diagnosis of metastasis and pulmonary involvement did not influence OSM+. We did not observe any substantial treatment progress. A comparison of the present cohort with 84 GBM/ GS patients with exclusive CNS dissemination suggests that metastases outside the CNS are related to a slightly more favorable outcome.
The occurrence of extra-CNS metastasis from GBM/ GS is associated with a dismal prognosis, however it seems to compare slightly favorable to CNS dissemination. Crucial treatment progress has not been achieved over recent decades. A central registry should be considered to consecutively gain more information about the ideal therapeutic approach.
确定多形性胶质母细胞瘤(GBM)或胶质肉瘤(GS)患者发生中枢神经系统(CNS)以外转移的特征、治疗方法及预后。
使用关键词胶质肉瘤、胶质母细胞瘤、GBM、转移、转移灶和转移性,在PubMed和Web of Science上检索有关GBM/GS患者发生转移播散的同行评审文章。此外,我们还根据所选论文的参考文献进行了手工检索。排除发生CNS转移的病例,并在另一项研究中进行评估。
1928年至2013年间发表的109篇文章符合要求。这些文章报道了150例患者。我们观察到每十年的病例数随时间显著增加。转移灶诊断后的中位总生存期(OSM+)为6.0±0.8个月,初始诊断后的中位总生存期(OSID)为13±2.4个月。单因素分析显示,性别、年龄、组织学亚型、初始诊断与转移灶诊断之间的时间间隔以及肺部受累情况均不影响OSM+。我们未观察到任何实质性的治疗进展。将本队列与84例仅发生CNS播散的GBM/GS患者进行比较,结果表明CNS以外的转移灶与略好的预后相关。
GBM/GS发生CNS以外转移与预后不良相关,但似乎比CNS播散略好。近几十年来尚未取得关键的治疗进展。应考虑建立一个中央登记处,以便持续获取更多关于理想治疗方法的信息。