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. Author manuscript; available in PMC: 2021 Dec 9.
Published in final edited form as: Int J Radiat Oncol Biol Phys. 2020 Jun 27;108(4):979–986. doi: 10.1016/j.ijrobp.2020.06.020

Table 1.

Participant demographics for the BEV group, BEV/pRDR group, and all participants combined

BEV BEV/pRDR All
Patients, n (%) 47 (59) 33 (41) 80 (100)
OS Censored, n (%) 8 (17) 7 (21) 15 (19)
  Alive, n (%) 2 (4) 3 (9) 5 (6)
  Withdrawal, n (%) 6 (13) 4 (12) 10 (13)
PFS censored, n (%) 8 (17) 7 (21) 15 (19)
 Progression free, n (%) 0 (0) 1 (3) 1 (1)
 Withdrawal, n (%) 8 (17) 6 (18) 14 (18)
Age, median (range), y 60 (23–79) 42 (26–71) 53 (23–79)
Male sex, n (%) 28 (60) 19 (58) 47 (59)
KPS, median (range) 70 (40–100) 80 (60–100) 70 (40–100)
Pre-BEV resection,* n (%) 18 (38) 14 (42) 32 (40)
WHO grade III, n (%) 12 (26) 14 (42) 26 (33)
WHO grade IV, n (%) 35 (74) 19 (58) 54 (68)
Recurrences before 1 (1–4) 2 (1–4) 1 (1–4)
 BEV, median (range)
>9 cycles of BEV before progression, n (%) 3 (6) 3 (9) 6 (8)
Treatment(s) after progression,§ n (%) 24 (51) 15 (46) 39 (49)
 Bevacizumab, n 14 7 21
 Carmustine/ lomustine, n 6 10 16
  With bevacizumab, n 3 4 7
Interferon, n 1 0 1
Isotretinoin, n 9 3 12
Pembrolizumab, n 0 1 1
Surgery, n 2 0 2
Tamoxifen, n 1 0 1
Temozolomide, n 2 0 2

Abbreviations: max = maximum; OS = overall survival; PFS = progression-free survival; pRDR = pulsed reduced dose rate radiation therapy.

*

The number of participants who underwent surgical resection within 6 months prior to bevacizumab.

The number of tumor recurrences prior to bevacizumab.

The number of patients who continued bevacizumab at varied dosing and/or frequency beyond the standard full course while progression free.

§

The number of participants who received additional treatment after progression on either bevacizumab (BEV) or pRDR (BEV/pRDR). Tumor treating fields and other additional radiation therapy are not included because patients were censored from OS analysis when those therapies were initiated.