Abstract 459P
Background
Tumor Treating Fields (TTFields) therapy is approved for treatment of patients with newly diagnosed glioblastoma (ndGBM). Clinical trials have demonstrated statistically significant survival benefits when TTFields therapy is used alongside maintenance temozolomide. However, there is a lack of comprehensive real-world data examining the correlation between device usage and patient survival.
Methods
Utilizing electronic medical records from the xCures real-world data platform, this study analyzed ndGBM patients who began TTFields therapy in various US settings from January 1 to December 31, 2019. Device usage was quantified as the average percentage of time that the device was operational during the initial three months of therapy. Patients were categorized into three usage groups: high (≥75%), intermediate (50-75%), and low (<50% or <30 days, excluding patients identified as discontinuing due to disease progression or death). Statistical analysis included multivariate Cox regression and propensity score matching to adjust for confounders, with a data cutoff for analysis on March 18, 2024.
Results
The study included 1,944 patients, with 1,749 (90%) persisting with the therapy for at least 30 days. Out of 1,881 patients suitable for evaluation, 801 (43%) were high users, 553 (29%) intermediate users, and 527 (28%) low users. Baseline characteristics were consistent across groups, although high usage was slightly more common among older patients and females. Survival was significantly increased for the high use group (median OS benefit: 3.8 months; HR: 0.70; 95% CI: 0.62–0.80; P<0.001) and for the intermediate use group (median OS benefit: 2.1 months; HR: 0.85; 95% CI: 0.75–0.97; P=0.017) compared to the low use group. A matched cohort analysis was consistent with results from the unmatched analysis.
Conclusions
Consistent with controlled clinical trial results, these results confirm that higher TTFields device usage is associated with significantly improved survival outcomes in a broad real-world population of ndGBM patients. These findings underscore the importance of maintaining high adherence to TTFields therapy within clinical practice.
Clinical trial identification
Editorial acknowledgement
Editorial and submission support was provided by Curry Rockefeller Group, LLC, a Citrus Health Group, Inc., company (Chicago, IL) and funded by Novocure, Inc.
Legal entity responsible for the study
Novocure, Inc.
Funding
Novocure, Inc.
Disclosure
S. Cabezas-Camarero: Financial Interests, Personal, Other, Consulting fees: Merck-Serono, GSK; Financial Interests, Personal, Other, Speaker's Bureau: Bristol Myers Squibb, Merck-Serono, MSD; Financial Interests, Personal, Other, Travel and Academic work Fees: Merck-Serono, MSD, Janssen, and Bristol Myers Squibb; Financial Interests, Personal, Research Grant: AstraZeneca, GSK, MSD, Merck-Serono. N. Avgeropoulos: Financial Interests, Personal, Full or part-time Employment: Novocure. P. Conlon: Financial Interests, Personal, Full or part-time Employment: Novocure; Financial Interests, Personal, Stocks or ownership: Novocure. G.V. Chavez: Financial Interests, Personal, Full or part-time Employment: Novocure; Financial Interests, Personal, Stocks or ownership: Novocure; Financial Interests, Personal, Other, Computing/data management resources: Novocure. O. Farber: Financial Interests, Personal, Full or part-time Employment: Novocure; Financial Interests, Personal, Stocks or ownership: Novocure. All other authors have declared no conflicts of interest.
Resources from the same session
566P - Impact of weekly irinotecan’s cycles during preoperative chemoradiotherpy in locally advanced rectal cancer: A post-hoc analysis of the CinClare study
Presenter: Ji Zhu
Session: Poster session 16
567P - Interim endoscopic restaging after induction chemotherapy to predict complete response and survival after total neoadjuvant therapy in low rectal cancer: Ad-hoc analysis of the IMPACT trial
Presenter: Eiji Shinozaki
Session: Poster session 16
568P - Risk factors for recurrence after surgery for rectal cancer in a modern, nationwide population-based cohort
Presenter: Sepehr Doroudian
Session: Poster session 16
569P - Mismatch repair deficient, stage II/III rectal cancer: Real-world patient, tumour, and treatment characteristics in the Netherlands
Presenter: Renee Lunenberg
Session: Poster session 16
571P - Neoadjuvant chemotherapy with FOLFIRINOX and short course radiotherapy in locally advanced rectal caner (ISANOX): A prospective phase II trial
Presenter: Feryel Letaief-Ksontini
Session: Poster session 16
572P - Tolerance of adjuvant chemotherapy in older patients after resection of stage III colon adenocarcinoma from PRODIGE 34 – FFCD 1402 - ADAGE randomized phase III trial
Presenter: Thomas Aparicio
Session: Poster session 16
573P - M9140, an anti-CEACAM5 antibody drug conjugate (ADC), in patients with metastatic colorectal cancer (mCRC): Updated results from a phase I trial
Presenter: Valentina Boni
Session: Poster session 16
574P - First-in-class PD-1/IL-2 bispecific antibody fusion protein IBI363 + bevacizumab (beva) in patients (pts) with advanced colorectal cancer (CRC): A phase I study
Presenter: Zhen Yu Lin
Session: Poster session 16
575P - Phase Ib/II study of ompenaclid (RGX-202-01), a first-in-class oral inhibitor of the creatine transporter SLC6A8, in combination with FOLFIRI and bevacizumab (BEV) in RAS mutated (RASmt) second-line (2L) advanced/metastatic colorectal cancer (mCRC): Updated results
Presenter: Andrew Hendifar
Session: Poster session 16