Abstract 534P
Background
Treatment of glioblastoma patients under 70 years and with good Karnofski performance status (KPS>70) associates standard radiation therapy (SRT, 60 Gy in 30 fractions) with concomitant and adjuvant temozolomide for 6 monthly cycles (SRT-TMZ). Clinical trials of glioblastoma radiation treatment in patients older than 60 years (≥60-ys) showed no significant difference in survival comparing SRT to hypofractionated radiotherapy (HRT, 40.05 Gy in 15 fractions). Adding TMZ to HRT (HRT-TMZ) in patients ≥65-ys have translated into increased median overall survival (mOS) and progression-free survival (mPFS). In daily clinical practice, as in previous retrospective studies, older patients and/or those with KPS ≤70 may still be treated with radiation and temozolomide regardless of the MGMT tumor status, often opting for HRT-TMZ.
Methods
We retrospectively included all glioblastoma patients older than 60 years treated from 2017 to 2021 in our hospital with SRT-TMZ or HRT-TMZ. The primary endpoint was OS. The secondary endpoints were PFS, survival at 12 months (mo) and toxicity profile. Comparisons were made using Fisher´s exact test and Mann-Whitney test. Survival curves were estimated using the Kaplan-Meyer method and compared using the log-rank test.
Results
69 patients were treated, 33 with SRT-TMZ and 36 with HRT-TMZ. Median age was significantly different between these two groups (64 ys [range 60-70]) vs. 71 ys [range 62-85]), p<0.0001). KPS, extent of surgery, MGMT and IDH status did not show significant differences between groups. mPFS was 9 mo for SRT-TMZ vs. 10.2 mo for HRT-TMZ (p=0.57) and mOS was 14.8 mo vs. 13.8 mo (p=0.99), respectively. Treatment with SRT-TMZ was associated with increased thrombocytopenia events at the end of the first phase (p=0.01).
Conclusions
In real world, elderly glioblastoma patients pragmatically oriented to HRT-TMZ still had similar OS and PFS as younger patients treated with standard and potentially more toxic SRT-TMZ. This may support the extended use of HRT-TMZ in patients above 60 years.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
592P - The role of early change in circulating tumor DNA as a potential predictor of response to chemotherapy in patients with metastatic colorectal cancer
Presenter: Jinjia Chang
Session: Poster session 10
594P - The efficacy of anti-EGFR therapy for RAS mutant metastatic colorectal cancer (mCRC) patients with RAS mutation negative in circulating-tumor DNA (ctDNA) after 1st- or 2nd-line chemotherapy
Presenter: Naoki Izawa
Session: Poster session 10
595P - The DUREC trial: Durvalumab plus total neoadjuvant therapy in locally advanced rectal cancer - a multicenter, single-arm, phase II study (GEMCAD-1703)
Presenter: Jaume Capdevila Castillon
Session: Poster session 10
597P - Surgical quality for patients (pts) treated with neoadjuvant chemotherapy vs chemoradiation for locally advanced rectal cancer (LARC): PROSPECT (NCCTG N1048, alliance)
Presenter: Martin Weiser
Session: Poster session 10
598P - Influence of the early stoma closure after low rectal cancer resection on completeness of adjuvant chemotherapy (CoCStom): A randomized, controlled multicentre trial of the AIO (AIO KRK 0113)
Presenter: Flavius Sandra-Petrescu
Session: Poster session 10
599P - R-IMMUNE: A phase Ib/II study to evaluate safety and efficacy of atezolizumab combined with radio-chemotherapy in a preoperative setting for patients with locally advanced rectal cancer (LARC)
Presenter: Javier Carrasco
Session: Poster session 10