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. 2024 Mar 1;11(3):347–357. doi: 10.1093/nop/npae017

Table 2.

Patients With an Unfavorable Change Beyond Minimal Clinical Important Difference in Global Health Status at the 12-Month Follow-up Compared to All Other Patients (N = 51)

Variable Unfavorable Change Beyond MCID in Global
Health Status at 12-Month Follow-up
(N = 12)
All Other Patients
(N = 39)
P-value
Age at surgery, mean (SD) 48.1 (9.8) 41.5 (12.2) .07
Female, No (%) 5 (41.7) 21 (53.8) .52
KPS < 80 at admission, No (%) 1 (8.3) 5 (12.8) 1.0
Incidental, No (%) 2 (16.7) 6 (15.4) 1.0
History of seizures at admission, No (%) 8 (66.7) 26 (66.7) 1.0
Any neurological deficit at admission, No (%) 5 (41.7) 10 (25.6) .30
History of seizures at admission without any neurological deficit, No (%) 5 (41.7) 20 (51.3) .74
Tumor location, No (%)
 Mainly frontal 7 (58.3) 22 (56.4) 1.0
 Mainly temporal 1 (8.3) 8 (20.5) .67
 Other 4 (33.3) 9 (23.1) .47
Tumor laterality, mainly left hemisphere, No (%) 3 (25.0) 20 (51.3) .18
Choice of neurosurgical intervention, No (%)
 Tumor resection 12 (100) 36 (92.3) 1.0
Tumor type, oligodendroglioma, No (%) 8 (66.7) 18 (46.2) .32
Tumor grade, grade 2, No (%) 8 (66.7) 25 (64.1) 1.0
Treatment before 12-month follow-up
 Start chemotherapy (delta T in months), mean (SD) 4.5 (2.1) 4.4 (2.4) .93
 Start radiotherapy (delta T in months), mean (SD) 3.8 (2.4) 3.4 (2.6) .68
 None, No (%) 3 (25.0) 5 (12.8) .37
 Chemotherapy onlya, No (%) 0 (0) 5 (12.8) .32
 Radiochemotherapya,b, No (%) 9 (75.0) 29 (74.4) 1.0
Other treatment details
 Choice of chemotherapy first line drugs, temozolomide, No/N (%) 4/9 (44.4) 21/34 (61.8) .46
 Radiation type, proton, No/N (%) 7/9 (77.8) 25/29 (86.2) .61
 Radiation mean dose to the brain, GyRBEc, mean (SD) 14.4 (5.0) 14.1 (5.0) .85
Other relevant treatments and interventions, No/N (%)
 Antiepileptic drug use at 12-month follow-up* 10/11 (90.9) 23/35 (65.7) .14
 Physical rehabilitation* 4/11 (36.4) 5/39 (12.8) .09
Any permanent, new or worsened, neurological deficit, No (%) 5 (41.7) 7 (17.9) .12

aEither temozolomide, lomustine, or procarbazine hydrochloride, lomustine and vincristine (PCV).

bEither concomitant or adjuvant.

cBiologic equivalent dose with fractions of 2Gy (α/β3).

*Observe missing data.