Efficacy and Safety of Tumor Treating Fields (TTFields) in Elderly Patients with Newly Diagnosed Glioblastoma: Subgroup Analysis of the Phase 3 EF-14 Clinical Trial.

BACKGROUND

Understudied elderly patients comprise a large segment of high-risk patients with glioblastoma (GBM) that are challenging to treat. Tumor Treating Fields (TTFields) is a locoregional, noninvasive, antimitotic therapy delivering low-intensity, intermediate-frequency alternating electric fields to the tumor. In the phase 3 EF-14 clinical trial, TTFields (200 kHz) improved median progression-free survival (PFS) and median overall survival (OS) in patients with newly diagnosed GBM (ndGBM) when added concomitantly to maintenance temozolomide (TMZ). This EF-14 subgroup analysis evaluated the safety and efficacy of TTFields in elderly patients.

METHODS

All 134 patients who are ≥65 years of age were included (TTFields/TMZ combination, n=89; TMZ monotherapy, n=45; 2:1 ratio of randomization). PFS and OS were analyzed using Kaplan-Meier methodology (α=0.05). Health-related quality-of-life (HRQoL) was assessed using the European Organisation for Research and Treatment of Cancer (EORTC) quality-of-life questionnaire QLQ-C30 supplemented with the brain tumor module (QLQ-BN20). Adverse events (AEs) were evaluated using Common Terminology Criteria for AEs (CTCAE) v4.0.

RESULTS

The PFS was 6.5 months in patients randomized to the treatment group with TTFields/TMZ combination

CONCLUSIONS

Combining TTFields with maintenance TMZ significantly improved PFS and OS in elderly patients with ndGBM in the phase 3 EF-14 clinical trial, without significant increases in systemic toxicity or negatively affecting patient HRQoL. TTFields-related skin AEs were low-grade and manageable.

CLINICAL TRIAL REGISTRATION

https://clinicaltrials.gov/ct2/show/NCT00916409, identifier: NCT00916409.

Informations de copyright

Copyright © 2021 Ram, Kim, Hottinger, Idbaih, Nicholas and Zhu.

Déclaration de conflit d'intérêts

ZR received research grants from and is a paid consultant of Novocure. AH received a research grant from Novocure, paid to the institution. AI received research grants and travel funding from Carthera, Leo Pharma and Novocure, research grants from Air Liquide, Nutritheragene, Sanofi, and Transgene, and travel funding from Leo Pharma, and served on received honorarium for advisory boards from Novocure and Leo Pharma. J-JZ received funding paid to the institution from Boston Biomedical Sumitomo Dainippon Pharma Global Oncology, Novocure, Inc., and NRG consortium of National Cancer Institute (NCI) and an honorarium from the Hong Kong Precision Oncology Society. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The authors declare that this study received funding from Novocure. The funder had the following involvement with the study: design and conduct of the study; collection, management, analysis, andinterpretation of the data; and preparation and review of this manuscript.