Evidence map›Paper›PMID 29392280›Full record

Trial reportJAMA oncology2018

Influence of Treatment With Tumor-Treating Fields on Health-Related Quality of Life of Patients With Newly Diagnosed Glioblastoma: A Secondary Analysis of a Randomized Clinical Trial.

Martin J B Taphoorn, Linda Dirven, Andrew A Kanner, Gitit Lavy-Shahaf, Uri Weinberg, Sophie Taillibert, Steven A Toms, Jerome Honnorat, Thomas C Chen, Jan Sroubek and 13 more

6 registry-linked trialsAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 6 registered trials, which are not on this map. Cited by 128 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed, 5 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00916409 phase3completednot on this map

A Prospective, Multi-center Trial of NovoTTF-100A Together With Temozolomide Compared to Temozolomide Alone in Patients With Newly Diagnosed GBM.

TypeinterventionalSponsorNovoCure Ltd.Ran2009 to 2017Enrolled700ConditionsGlioblastoma MultiformeArmsNovoTTF-100A device, Temozolomide
NCT03940196 phase3completednot on this mapstarted 2019, after this paper: background citation

ENGOT-ov50 / GOG-3029 / INNOVATE-3: Pivotal, Randomized, Open-label Study of Tumor Treating Fields (TTFields, 200kHz) Concomitant With Weekly Paclitaxel for the Treatment of Recurrent Ovarian Cancer

TypeinterventionalSponsorNovoCure Ltd.Ran2019 to 2023Enrolled540ConditionsOvarian CancerArmsNovoTTF-100L(O), Paclitaxel
NCT04281576 nacompletednot on this mapstarted 2019, after this paper: background citation

A Phase 2, Single Arm, Multi-center, Open-Label Trial to Evaluate the Safety and Efficacy of Treatment with Tumor Treating Fields (TTFields) and Chemotherapy As First-Line Treatment for Subjects with Unresectable Gastroesophageal Junction (GEJ) Adenocarcinoma or Gastric (GC) Adenocarcinoma

TypeinterventionalSponsorNovoCure Ltd.Ran2019 to 2024Enrolled28ConditionsGastric Cancer, GastroEsophageal CancerArmsNovoTTF-100L(P), Oxaliplatin, Capecitabine, Trastuzumab
NCT04492163 phase2completednot on this mapstarted 2020, after this paper: background citation

EF-33: An Open-Label Pilot Study of OPTUNE® (TTFields, 200 Khz) With High Density Transducer Arrays for the Treatment of Recurrent Glioblastoma

TypeinterventionalSponsorNovoCure GmbHRan2020 to 2023Enrolled25ConditionsGlioblastoma MultiformeArmsTTFields
NCT04717739 unknown statusnot on this mapstarted 2021, after this paper: background citation

Use of TTFields in Germany in Routine Clinical Care Study PROgram - Daily Activity, Sleep and Neurocognitive Functioning in Newly Diagnosed Glioblastoma Patients Study

TypeobservationalSponsorNovoCure Ltd.Ran2021 to 2025Enrolled500ConditionsGlioblastomaArmsTTFields
NCT04892472 phase2terminatednot on this mapstarted 2021, after this paper: background citation

EF-36/Keynote B36: A Pilot, Randomized, Open-label Study of Tumor Treating Fields (TTFields, 150 kHz) Concomitant With Pembrolizumab for First Line Treatment of Advanced or Metastatic Non-small Cell Lung Cancer

TypeinterventionalSponsorNovoCure GmbHRan2021 to 2025Enrolled15ConditionsNon-small Cell Lung CancerArmsNovoTTF-200T, Pembrolizumab (MK-3475) 200 mg
3 · Its place in the literature

Who cites it

128 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
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  4. Time to deterioration in cancer randomized clinical trials for patient-reported outcomes data: a systematic review.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2020
    Pooled it
  5. Pooled it
  6. Trial
  7. Cancer-specific utility: clinical validation of the EORTC QLU-C10D in patients with glioblastoma.The European journal of health economics : HEPAC : health economics in prevention and care · 2025
    Trial
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  9. Article
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  13. Neuromodulation in Neuro-Oncology: A Scoping Review.Journal of personalized medicine · 2026
    Review
  14. Review
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  17. Post-recurrence management of malignant glial brain tumors: therapeutic strategies, evidence and limitations, palliative care, terminal sedation, and end-of-life considerations.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  18. Article
  19. Article
  20. Review

68 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors.

Martin J B TaphoornDepartment of Neurology, Haaglanden Medical Center, The Hague, The Netherlands.
Linda DirvenDepartment of Neurology, Haaglanden Medical Center, The Hague, The Netherlands.
Andrew A KannerDepartment of Neurosurgery, Rabin Medical Center, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Gitit Lavy-ShahafResearch and Development, Novocure, Haifa, Switzerland.
Uri WeinbergResearch and Development, Novocure, Haifa, Switzerland.
Sophie TaillibertDepartment of Neurology 2, Salpêtrière University Hospital, Assistance Public Hôpitaux de Paris, L'Université Pierre et Marie Curie University, Paris VI University, Paris, France.
Steven A TomsDepartment of Neurosurgery, Geisinger Medical Center, Danville, Pennsylvania.
Jerome HonnoratDepartment of Neuro-oncology, Hospices Civils de Lyon, University Claude Bernard Lyon, Lyon, France.
Thomas C ChenDepartment of Neurosurgery, University of Southern California, Los Angeles.
Jan SroubekDepartment of Neurosurgery, Na Homolce Hospital, Prague, Czech Republic.
Carlos DavidDepartment of Neurosurgery, Lahey Clinic, Burlington, Massachusetts.
Ahmed IdbaihDepartment of Neurology 2, Salpêtrière University Hospital, Assistance Public Hôpitaux de Paris, L'Université Pierre et Marie Curie University, Paris VI University, Paris, France.
Jacob C EasawDepartment of Medical Oncology, Cross Cancer Institute, Edmonton, California.
Chae-Yong KimDepartment of Neurosurgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Bundang, Korea.
Jordi BrunaDepartment of Neurology, Hospital Universitari Bellvitge, Barcelona, Spain.
Andreas F HottingerDepartment of Medical Oncology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
Yvonne KewClinical Neuro-Oncology Research Program, Department of Internal Medicine, Methodist Hospital, Houston, Texas.
Patrick RothDepartment of Neurology, University of Zurich, Zurich, Switzerland.
Rajiv DesaiNeurosurgery and Spine Association, Maine Medical Center, Scarborough, Maine.
John L VillanoClinical Neuro-Oncology Research Program, Department of Internal Medicine, University of Kentucky Medical Center, Lexington.
Eilon D KirsonResearch and Development, Novocure, Haifa, Switzerland.
Zvi RamDepartment of Neurosurgery, Tel Aviv Medical Center, Tel Aviv University, Tel Aviv, Israel.
Roger StuppRobert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importanceTumor-treating fields (TTFields) therapy improves both progression-free and overall survival in patients with glioblastoma. There is a need to assess the influence of TTFields on patients' health-related quality of life (HRQoL).

objectiveTo examine the association of TTFields therapy with progression-free survival and HRQoL among patients with glioblastoma. DESIGN, SETTING, AND

participantsThis secondary analysis of EF-14, a phase 3 randomized clinical trial, compares TTFields and temozolomide or temozolomide alone in 695 patients with glioblastoma after completion of radiochemotherapy. Patients with glioblastoma were randomized 2:1 to combined treatment with TTFields and temozolomide or temozolomide alone. The study was conducted from July 2009 until November 2014, and patients were followed up through December 2016.

interventionsTemozolomide, 150 to 200 mg/m2/d, was given for 5 days during each 28-day cycle. TTFields were delivered continuously via 4 transducer arrays placed on the shaved scalp of patients and were connected to a portable medical device. MAIN OUTCOMES AND MEASURES: Primary study end point was progression-free survival; HRQoL was a predefined secondary end point, measured with questionnaires at baseline and every 3 months thereafter. Mean changes from baseline scores were evaluated, as well as scores over time. Deterioration-free survival and time to deterioration were assessed for each of 9 preselected scales and items.

resultsOf the 695 patients in the study, 639 (91.9%) completed the baseline HRQoL questionnaire. Of these patients, 437 (68.4%) were men; mean (SD) age, 54.8 (11.5) years. Health-related quality of life did not differ significantly between treatment arms except for itchy skin. Deterioration-free survival was significantly longer with TTFields for global health (4.8 vs 3.3 months; P < .01); physical (5.1 vs 3.7 months; P < .01) and emotional functioning (5.3 vs 3.9 months; P < .01); pain (5.6 vs 3.6 months; P < .01); and leg weakness (5.6 vs 3.9 months; P < .01), likely related to improved progression-free survival. Time to deterioration, reflecting the influence of treatment, did not differ significantly except for itchy skin (TTFields worse; 8.2 vs 14.4 months; P < .001) and pain (TTFields improved; 13.4 vs 12.1 months; P < .01). Role, social, and physical functioning were not affected by TTFields. CONCLUSIONS AND RELEVANCE: The addition of TTFields to standard treatment with temozolomide for patients with glioblastoma results in improved survival without a negative influence on HRQoL except for more itchy skin, an expected consequence from the transducer arrays.

trial registrationclinicaltrials.gov Identifier: NCT00916409.

Indexed as

Physical Therapy ModalitiesQuality of LifeTranscranial Direct Current StimulationAdultAgedAged, 80 and overBrain NeoplasmsChemoradiotherapyCombined Modality TherapyCytoreduction Surgical ProceduresDisease-Free SurvivalFemaleFollow-Up StudiesGlioblastomaHealth StatusHumansTemozolomide

Identifiers

PMID29392280
PMCPMC5885193

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.