(WO/2009/044289) TREATING CANCER USING ELECTROMAGNETIC FIELDS IN COMBINATION WITH PHOTODYNAMIC THERAPY
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Latest bibliographic data on file with the International Bureau | ||||||||||||
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IPC: | A61N 5/06 (2006.01), A61N 1/40 (2006.01) | |||||||||||
Applicants: | NOVOCURE LTD. [IL/IL]; Po Box 15022, Matam Center, 319805 Haifa (IL) (All Except US). PALTI, YORAM [IL/IL]; (IL) (US Only). | |||||||||||
Inventor: | PALTI, YORAM; (IL). | |||||||||||
Priority Data: |
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Disruption of Cancer Cell Replication by Alternating Electric Fields
[CANCER RESEARCH 64, 3288–3295, May 1, 2004]
Eilon D. Kirson,1 Zoya Gurvich,2 Rosa Schneiderman,2 Erez Dekel,3 Aviran Itzhaki,4 Yoram Wasserman,1,4
Rachel Schatzberger,2 and Yoram Palti2
1Department of Biomedical Engineering, NovoCure Ltd., Haifa, Israel; 2B. Rappaport Faculty of Medicine, Technion—Israel Institute of Technology, Haifa, Israel; 3Department
of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel; and 4Elisha Medical Centre, Haifa, Israel
ABSTRACT
Low-intensity, intermediate-frequency (100–300 kHz), alternating electric
fields, delivered by means of insulated electrodes, were found to have
a profound inhibitory effect on the growth rate of a variety of human and
rodent tumor cell lines (Patricia C, U-118, U-87, H-1299, MDA231, PC3,
B16F1, F-98, C-6, RG2, and CT-26) and malignant tumors in animals.
This effect, shown to be nonthermal, selectively affects dividing cells while
quiescent cells are left intact. These fields act in two modes: arrest of cell
proliferation and destruction of cells while undergoing division. Both
effects are demonstrated when such fields are applied for 24 h to cells
undergoing mitosis that is oriented roughly along the field direction. The
first mode of action is manifested by interference with the proper formation
of the mitotic spindle, whereas the second results in rapid disintegration
of the dividing cells. Both effects, which are frequency dependent, are
consistent with the computed directional forces exerted by these specific
fields on charges and dipoles within the dividing cells. In vivo treatment of
tumors in C57BL/6 and BALB/c mice (B16F1 and CT-26 syngeneic tumor
models, respectively), resulted in significant slowing of tumor growth and
extensive destruction of tumor cells within 3–6 days. These findings
demonstrate the potential applicability of the described electric fields as a
novel therapeutic modality for malignant tumors.
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