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. 2022 Feb 26;9(4):271–283. doi: 10.1093/nop/npac016

Table 1.

Participants’ Sociodemographic, Clinical, and Neurocognitive Characteristics

Patients Proxies
Participants, N 81 81
Sex (male), N (%) 32 (39.5%) 32 (39.5%)
Age, mean (SD) 58.2 (11.7) 57.7 (11.7)
Level of education [1–8], median [range] 3 [1–8] 4 [1–7]
Type of proxy, N (%)
Partner 60 (74.1%)
Other (e.g. parent/child/sibling) 21 (25.9%)
Duration relationship (in yrs), mean (SD) 32.9 (14.20)
Tumor type, N (%)
Glioma 43 (53.1%)
Diffuse astrocytoma, IDH-mutant + 1p/19q noncodeleted 2 (4.7%)
Diffuse astrocytoma, IDH-mutant + unknown 1p/19q-codeletion 2 (4.7%)
Oligodendroglioma, IDH-mutant + 1p/19q-codeleted 2 (4.7%)
Diffuse astrocytoma, IDH-wildtype 1 (2.3%)
Diffuse astrocytoma, NOS 11 (25.6%)
Anaplastic astrocytoma, IDH-mutant 1 (2.3%)
Anaplastic oligodendroglioma, 1p/19p-codeleted 4 (9.3%)
Anaplastic glioma, NOS 2 (4.7%)
Glioblastoma, IDH-mutant 1 (2.3%)
Glioblastoma, IDH-wildtype 10 (23.3%)
Glioblastoma, NOS 7 (16.3%)
Brain metastases 38 (46.9%)
1-3 brain metastases 21 (25.9%)
>3 brain metastases 17 (21.0%)
Tumor location, N (%)
Frontal 24 (29.6%)
Temporal 12 (14.8%)
Occipital 5 (6.2%)
Parietal 8 (9.9%)
Multiple 29 (35.8%)
Other 2 (2.5%)
Unreported 1 (1.2%)
KPS score, median [range] 80 [40-100]
Subjective neurocognitive complaints (MOS COG–R), median [range] 29 [6-36]
Above average subjective neurocognitive complaints (MOS COG–R), N (%) 56 (69.1%)
Treatment status (active anti-tumor treatment), N (%) 24 (29.6%)
Neurocognitively impaired, N (%) 37 (45.7%)
Direct recall impaired, N (%) 21 (25.9%)
Delayed recall impaired, N (%) 25 (30.9%)
Recognition discrimination impaired, N (%) 8 (9.9%
Information processing speed impaired, N (%) 22 (27.2%)
Cognitive flexibility impaired, N (%) 45 (55.6%)
Verbal fluency impaired, N (%) 18 (22.2%)

N, number; SD, standard deviation; yrs, years; LGG, low grade glioma; HGG, high grade glioma; KPS, Karnofsky Performance Score; MOS COG–R, Medical Outcomes Study Cognitive Functioning Scale–Revised.