» Articles » PMID: 19387848

Alternating Electric Fields (TTFields) Inhibit Metastatic Spread of Solid Tumors to the Lungs

Overview
Specialty Oncology
Date 2009 Apr 24
PMID 19387848
Citations 65
Authors
Affiliations
Soon will be listed here.
Abstract

Tumor treating fields (TTFields) are low intensity, intermediate frequency, alternating electric fields used to treat cancerous tumors. This novel treatment modality effectively inhibits the growth of solid tumors in vivo and has shown promise in pilot clinical trials in patients with advanced stage solid tumors. TTFields were tested for their potential to inhibit metastatic spread of solid tumors to the lungs in two animal models: (1) Mice injected with malignant melanoma cells (B16F10) into the tail vein, (2) New Zealand White rabbits implanted with VX-2 tumors within the kidney capsule. Mice and rabbits were treated using two-directional TTFields at 100-200 kHz. Animals were either monitored for survival, or sacrificed for pathological and histological analysis of the lungs. The total number of lung surface metastases and the absolute weight of the lungs were both significantly lower in TTFields treated mice then in sham control mice. TTFields treated rabbits survived longer than sham control animals. This extension in survival was found to be due to an inhibition of metastatic spread, seeding or growth in the lungs of TTFields treated rabbits compared to controls. Histologically, extensive peri- and intra-tumoral immune cell infiltration was seen in TTFields treated rabbits only. These results raise the possibility that in addition to their proven inhibitory effect on the growth of solid tumors, TTFields may also have clinical benefit in the prevention of metastatic spread from primary tumors.

Citing Articles

Impact of alternating electric fields therapy for newly diagnosed WHO grade 4 astrocytoma on patient survival: a real-world propensity-score adjusted prospective multicenter study.

Woo P, Pu J, Li L, Wong D, Hui V, Chan D J Neurooncol. 2025; .

PMID: 40067514 DOI: 10.1007/s11060-025-04985-3.


Tumor-treating fields and concurrent cisplatin: an demonstration of efficacy in triple-negative breast cancer.

Smothers A, Beasley M, Warren H, Kegel O, Edenfield W, OConnell J Am J Cancer Res. 2025; 15(1):322-330.

PMID: 39949927 PMC: 11815381. DOI: 10.62347/LXJH5896.


Enhancing immunotherapy efficacy with synergistic low-dose radiation in metastatic melanoma: current insights and prospects.

Rafiq Z, Kang M, Barsoumian H, Manzar G, Hu Y, Leuschner C J Exp Clin Cancer Res. 2025; 44(1):31.

PMID: 39881333 PMC: 11781074. DOI: 10.1186/s13046-025-03281-2.


The Synergy of Thermal and Non-Thermal Effects in Hyperthermic Oncology.

Minnaar C, Szigeti G, Szasz A Cancers (Basel). 2024; 16(23).

PMID: 39682096 PMC: 11639953. DOI: 10.3390/cancers16233908.


Intratumoral Treatment in Lung Cancer: Is It Time to Move Towards Clinical Practice?.

Pagliari G, Colonese F, Canova S, Abbate M, Sala L, Petrella F Cancers (Basel). 2024; 16(23).

PMID: 39682081 PMC: 11639858. DOI: 10.3390/cancers16233892.


References
1.
Lavrenkov K, Man S, Geffen D, Cohen Y . Experience of hormonal therapy with anastrozole for previously treated metastatic breast cancer. Isr Med Assoc J. 2002; 4(3):176-7. View

2.
Suresh S . Biomechanics and biophysics of cancer cells. Acta Biomater. 2007; 3(4):413-38. PMC: 2917191. DOI: 10.1016/j.actbio.2007.04.002. View

3.
Dunn G, Bruce A, Ikeda H, Old L, Schreiber R . Cancer immunoediting: from immunosurveillance to tumor escape. Nat Immunol. 2002; 3(11):991-8. DOI: 10.1038/ni1102-991. View

4.
vanSonnenberg E, Shankar S, Morrison P, Nair R, Silverman S, Jaklitsch M . Radiofrequency ablation of thoracic lesions: part 2, initial clinical experience--technical and multidisciplinary considerations in 30 patients. AJR Am J Roentgenol. 2005; 184(2):381-90. DOI: 10.2214/ajr.184.2.01840381. View

5.
Whiteside T . The tumor microenvironment and its role in promoting tumor growth. Oncogene. 2008; 27(45):5904-12. PMC: 3689267. DOI: 10.1038/onc.2008.271. View