Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster session 16

460P - Exploring the efficacy and optimal timing of tumor treating fields in newly diagnosed glioblastoma: A real-world study

Date

14 Sep 2024

Session

Poster session 16

Topics

Clinical Research;  Survivorship

Tumour Site

Central Nervous System Malignancies

Presenters

Zelei Dai

Citation

Annals of Oncology (2024) 35 (suppl_2): S406-S427. 10.1016/annonc/annonc1587

Authors

Z. Dai1, Y. Liu2, J. Yin3, Y. Zhang4, R. Qiu5, G. Li6, R. Liu7, X. Li8, D. Liu5, H. Li6, X. Zhang6, F. Wang1, X. Wang2, P. Ai1, Z. Li8, Q. Mao2, L. Liu1

Author affiliations

  • 1 Division Of Head & Neck Tumor Multimodality Treatment, Cancer Center, West China Hospital of Sichuan Univeristy, 610041 - Chengdu/CN
  • 2 Department Of Neurosurgery, West China Hospital of Sichuan Univeristy, 610041 - Chengdu/CN
  • 3 Department Of Radiation Oncology, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, 610000 - Chengdu/CN
  • 4 Department Of Evidence Based Medicine And Clinical Epidemiology, West China Hospital of Sichuan Univeristy, 610041 - Chengdu/CN
  • 5 Department Of Radiation Oncology, Henan Cancer Hospital/Affiliated Cancer Hospital of Zhengzhou University, 450008 - Zhengzhou/CN
  • 6 Department Of Radiation Oncology, The First Affiliated Hospital of Zhengzhou University, 450052 - Zhengzhou/CN
  • 7 Department Of Radiotherapy, TheFirstAffiliatedHospitalofXianJiaotongUniversity, 710061 - Xian/CN
  • 8 Department Of Radiation Oncology, Shenzhen People's Hospital, Jinan University, 518020 - Shenzhen/CN

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 460P

Background

The real-world performance of TTFields for newly diagnosed glioblastoma in the Chinese patient population, as well as if an earlier introduction at the concurrent usage with radiotherapy (RT) and temozolomide (TMZ) brings further benefit remains unclear.

Methods

This study emulates the design of the EF-14 and EF-32 randomized clinical trials. Patients with GBM who had undergone surgery from January 2019 to June 2023 were extracted from the Electronic Hospital System of 6 grade A tertiary teaching hospitals in China and followed up till January 2024. For expanded EF-14 emulation, individuals from the West China Hospital were duplicated, and each replicate was assigned to either the strategy “TTFields start during peri-RT period” or “no TTFields therapy.” For EF-32 emulation, individuals who’s had TTFields from all centers were duplicated, and assigned to “TTFields start with RT/TMZ” or “TTFields start with maintenance TMZ”. For each group, TTFields should last for at least 2 months. Replicates were censored when they failed to follow their assigned strategy, and potential selection bias was adjusted for by inverse-probability censoring weighting. Missing data were calculated by multiple imputation.

Results

Emulation of EF-14 led to 154 eligible patients (median age, 51.5 years; range, 20-80; 97 men [63%]). Real-world effect sizes of the emulated trial were close to EF-14 trial, with median overall survival from RT registration was 31.0 months in the TTFields group and 16.0 months in the non-TTFields group (HR, 0.54; 95% CI, 0.32-0.89; P = 0.017). Emulation of modified EF-32 led to 95 eligible patients (median age, 52 years; range, 21-80; 60 men [63.2%]). There was no significant difference in the duration of ovrall survival between the TTFields/RT/TMZ group and TTFields/TMZ group (median, 23.1 and 21.5 months; HR, 0.62; 95% CI, 0.28-1.39; P = 0.2).

Conclusions

Real-world data have bolstered the application of TTFields as an adjunct to the peri-RT period of the Stupp protocol. Although the difference in median overall survival between the TTFields/RT/TMZ and TTFields/TMZ groups was not statistically significant, it suggests an underlying potential to optimize treatment combinations as we anticipate the results of EF-32.

Clinical trial identification

NCT06346821, release date: April 4, 2024.

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.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.