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. 2019 Oct 17;10(25):6314–6326. doi: 10.7150/jca.33463

Table 1.

Demographic and clinical characteristics of German patients with pediatric low-grade glioma (n=1587)

median (min / max)
Age at diagnosis [years] 7.60 (0.10 / 17.90)
Age-group at diagnosis [years] total (n) (%)
<1 75 (4.7)
1-711/12 748 (47.1)
≥ 8 764 (48.1)
Sex
Female 740 (46.6)
Male 847 (53.4)
Main location at diagnosis
Cerebral hemispheres 320 (20.2)
Supratentorial midline 580 (36.6)
Cerebellum 467 (29.4)
Caudal brain stem 119 (7.5)
Spinal cord 56 (3.5)
Lateral ventricles 44 (2.8)
Initially disseminated 1 (0.1)
Main histology at diagnosis
Pilocytic Astrocytoma WHO I 869 (54.8)
Diffuse Astrocytoma WHO II 136 (8.6)
Oligodendroglioma WHO II 4 (0.3)
Oligoastrocytoma WHO II 8 (0.5)
Neuronal and mixed neuronal-glial tumors 203 (12.8)
Low-grade neuroepithelial or glial lesions not otherwise specified [LGG-NOS] 63 (4.0)
No histology/radiologic diagnosis-only 304 (19.2)
Neurofibromatosis [NF] status
NF negative 1352 (85.2)
NF-1 233 (14.7)
NF-2 2 (0.1)
Tuberous sclerosis complex [TSC]
TSC negative 1561 (98.4)
TSC positive* 26 (1.6)
Extent of resection at 1st surgery (n=1283)
Complete resection 522 (32.9)
Subtotal resection 138 (8.7)
Partial resection 360 (22.7)
Biopsy-only 263 (16.6)

1587 patients with pediatric low-grade glioma [PLGG] treated in Germany between 01.04.2004 and 31.03.2012 and followed until 27.04.2016 in the International Society of Paediatric Oncology - Low Grade Glioma subcommittee [SIOP-LGG] 2004 study. The percentage (%) of patients is given in brackets in respect to the whole group. * treatment with everolimus for subependymal giant cell astrocytoma in TSC patients was not documented, they remained in the observation group.