TY - JOUR
T1 - Health-related quality of life in patients with progressive glioblastoma treated with combined bevacizumab and lomustine versus lomustine only
T2 - Secondary outcome of the randomized phase III EORTC 26101 study
AU - Dirven, Linda
AU - Machingura, Abigirl
AU - van den Bent, Martin J.
AU - Coens, Corneel
AU - Bottomley, Andrew
AU - Brandes, Alba A.
AU - Domont, Julien
AU - Idbaih, Ahmed
AU - Koekkoek, Johan A. F.
AU - Reijneveld, Jaap C.
AU - Platten, Michael
AU - Wick, Wolfgang
AU - Taphoorn, Martin J. B.
N1 - Publisher Copyright:
© 2024 The Author(s). Published by Oxford University Press on behalf of the Society for Neuro-Oncology and the European Association of Neuro-Oncology.
PY - 2025/4/1
Y1 - 2025/4/1
N2 - Background: Progression-free survival, but not overall survival, was prolonged with bevacizumab and lomustine compared to lomustine only in the randomized phase 3 European Organization for Research and Treatment of Cancer (EORTC) 26101 study.Objective: To evaluate the impact of treatment on health-related quality of life (HRQoL) in progressive glioblastoma patients participating in the EORTC 26101 study.Methods: Patients with progressive glioblastoma, after standard radio-chemotherapy, were 2:1 randomized to either BEV/LOM or LOM. HRQoL was a secondary trial outcome and assessed using the EORTC QLQ-C30 and QLQ-BN20 questionnaires at baseline, and subsequently every 12 weeks. Predefined scales for analysis were global health status (GH), physical functioning, social functioning (SF), motor dysfunction, and communication deficit. The primary endpoint was HRQoL during the last assessment up to week 36. Moreover, time to HRQoL deterioration (TTD) and HRQoL deterioration-free survival (DFS) were calculated.Results: Out of 437 patients, 402 (92%) patients had a baseline HRQoL assessment, which dropped to 66% at week 36. During the last assessment up to week 36, no differences were observed for predefined scales, apart from SF being clinically relevant lower in the combination arm (mean 66.0 versus 81.0, p=.001). Of note, the baseline SF score was 66.4 for patients in the combination arm, showing stable SF. Median DFS was significantly longer in the combination arm (12.4 weeks) compared to lomustine alone (6.7 weeks), reflecting the difference in time to progression between arms. TTD, not including progression as an event, was not different between treatment arms (median 13.0 versus 12.9 weeks).Conclusion: The addition of bevacizumab to lomustine did not negatively affect HRQoL during the progression-free period.
AB - Background: Progression-free survival, but not overall survival, was prolonged with bevacizumab and lomustine compared to lomustine only in the randomized phase 3 European Organization for Research and Treatment of Cancer (EORTC) 26101 study.Objective: To evaluate the impact of treatment on health-related quality of life (HRQoL) in progressive glioblastoma patients participating in the EORTC 26101 study.Methods: Patients with progressive glioblastoma, after standard radio-chemotherapy, were 2:1 randomized to either BEV/LOM or LOM. HRQoL was a secondary trial outcome and assessed using the EORTC QLQ-C30 and QLQ-BN20 questionnaires at baseline, and subsequently every 12 weeks. Predefined scales for analysis were global health status (GH), physical functioning, social functioning (SF), motor dysfunction, and communication deficit. The primary endpoint was HRQoL during the last assessment up to week 36. Moreover, time to HRQoL deterioration (TTD) and HRQoL deterioration-free survival (DFS) were calculated.Results: Out of 437 patients, 402 (92%) patients had a baseline HRQoL assessment, which dropped to 66% at week 36. During the last assessment up to week 36, no differences were observed for predefined scales, apart from SF being clinically relevant lower in the combination arm (mean 66.0 versus 81.0, p=.001). Of note, the baseline SF score was 66.4 for patients in the combination arm, showing stable SF. Median DFS was significantly longer in the combination arm (12.4 weeks) compared to lomustine alone (6.7 weeks), reflecting the difference in time to progression between arms. TTD, not including progression as an event, was not different between treatment arms (median 13.0 versus 12.9 weeks).Conclusion: The addition of bevacizumab to lomustine did not negatively affect HRQoL during the progression-free period.
UR - http://www.scopus.com/inward/record.url?scp=105000817390&partnerID=8YFLogxK
U2 - 10.1093/nop/npae091
DO - 10.1093/nop/npae091
M3 - Article
C2 - 40110057
SN - 2054-2577
VL - 12
SP - 209
EP - 218
JO - Neuro-Oncology Practice
JF - Neuro-Oncology Practice
IS - 2
ER -