# An Evidence-Based Review of Alternating Electric Fields Therapy for Malignant Gliomas

**Authors:** Eric T Wong, Edwin Lok, Kenneth D. Swanson

PMC · DOI: 10.1007/s11864-015-0353-5 · 2015-07-05

## TL;DR

Alternating electric fields (TTFields) show promise as a new treatment for glioblastoma, with comparable or better results than chemotherapy and fewer side effects.

## Contribution

This paper reviews TTFields as a novel therapy for glioblastoma with a unique mechanism of action and favorable clinical outcomes.

## Key findings

- TTFields demonstrated equivalent efficacy to chemotherapy in recurrent glioblastoma without typical side effects.
- TTFields showed superiority over standard chemotherapy in early-stage glioblastoma treatment.
- Combining TTFields with other treatments may further improve outcomes.

## Abstract

Glioblastoma is a deadly disease and even aggressive neurosurgical resection followed by radiation and chemotherapy only extends patient survival to a median of 1.5 years. The challenge in treating this type of tumor stems from the rapid proliferation of the malignant glioma cells, the diffuse infiltrative nature of the disease, multiple activated signal transduction pathways within the tumor, development of resistant clones during treatment, the blood brain barrier that limits the delivery of drugs into the central nervous system, and the sensitivity of the brain to treatment effect. Therefore, new therapies that possess a unique mechanism of action are needed to treat this tumor. Recently, alternating electric fields, also known as tumor treating fields (TTFields), have been developed for the treatment of glioblastoma. TTFields use electromagnetic energy at an intermediate frequency of 200 kHz as a locoregional intervention and act to disrupt tumor cells as they undergo mitosis. In a phase III clinical trial for recurrent glioblastoma, TTFields were shown to have equivalent efficacy when compared to conventional chemotherapies, while lacking the typical side effects associated with chemotherapies. Furthermore, an interim analysis of a recent clinical trial in the upfront setting demonstrated superiority to standard of care cytotoxic chemotherapy, most likely because the subjects’ tumors were at an earlier stage of clonal evolution, possessed less tumor-induced immunosuppression, or both. Therefore, it is likely that the efficacy of TTFields can be increased by combining it with other anti-cancer treatment modalities.

## Linked entities

- **Diseases:** glioblastoma (MONDO:0018177)

## Full-text entities

- **Genes:** CALR (calreticulin) [NCBI Gene 811] {aka CALR1, CRT, HEL-S-99n, RO, SSA, cC1qR}, HMGB1 (high mobility group box 1) [NCBI Gene 3146] {aka HMG-1, HMG1, HMG3, SBP-1}, RAB3D (RAB3D, member RAS oncogene family) [NCBI Gene 9545] {aka D2-2, GOV, RAB16, RAD3D}, MYH14 (myosin heavy chain 14) [NCBI Gene 79784] {aka DFNA4, DFNA4A, FP17425, MHC16, MYH17, NMHC II-C}
- **Diseases:** non-small cell lung cancer (MESH:D002289), Cancer (MESH:D009369), neurological deficits (MESH:D009461), vomiting (MESH:D014839), hematological toxicities (MESH:D006402), Scalp (MESH:D004476), constipation (MESH:D003248), malignant pleural mesothelioma (MESH:D000086002), meningiomas (MESH:D008579), toxicities (MESH:D064420), Nervous system disorders (MESH:D009422), Malignant Gliomas (MESH:D005910), obstructive hydrocephalus (MESH:D006849), ovarian carcinoma (MESH:D010051), pineal meningioma (MESH:D010871), central nervous system malignancies (MESH:D002493), Gastrointestinal (MESH:D005767), diarrhea (MESH:D003967), nausea (MESH:D009325), Glioblastoma (MESH:D005909), convulsions (MESH:D012640), fatigue (MESH:D005221), appetite loss (MESH:D001068), pancreatic adenocarcinoma (MESH:D010190), lung metastases (MESH:D009362), pain (MESH:D010146),  (MESH:D001932),  (MESH:D009364)
- **Chemicals:** PRiDe (-), carboplatin (MESH:D016190), paclitaxel (MESH:D017239), cisplatin (MESH:D002945), dexamethasone (MESH:D003907), gemcitabine (MESH:D000093542), pemetrexed (MESH:D000068437), Temozolomide (MESH:D000077204), bevacizumab (MESH:D000068258)
- **Species:** Homo sapiens (human, species) [taxon 9606], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986]
- **Cell lines:** VX-2 tumors — Oryctolagus cuniculus (Rabbit), Rabbit neoplasm, Cancer cell line (CVCL_3864)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC4491358/full.md

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Source: https://tomesphere.com/paper/PMC4491358