Abstract Types

CRA
Clinical Review Abstract

LBA
Late-Breaking Abstract

TPS
Trials in Progress Abstract

e
Abstracts selected for publication but not presentation at the Annual Meeting

^
Abstracts granted an exception in accordance with ASCO's Conflict of Interest Policy



Overcoming cell size escape from tumor treating fields using a varying frequency treatment paradigm in vitro.

Sub-category:
New Targets and New Technologies

Category:
Tumor Biology

Meeting:
2013 ASCO Annual Meeting

Abstract No:
e22134

Citation:
J Clin Oncol 31, 2013 (suppl; abstr e22134)

Publication-only abstracts (abstract number preceded by an "e"), published in conjunction with the 2013 Annual Meeting but not presented at the Meeting, can be found online only.

Author(s): Rosa S. Schneiderman, Moshe Giladi, Yaara Porat, Mijal Munster, Uri Weinberg, Eilon David Kirson, Yoram Palti; NovoCure, Haifa, Israel; NovoCure, Lausanne, Switzerland

Abstract Disclosures


Abstract:

Background: TTFields Therapy at 200 kHz received FDA approval for the treatment of patients with recurrent glioblastoma (GBM) based on the results of a phase III clinical trial. Radiological responses were observed in 14% of the treated patients. The lack of radiological response in the remaining patients suggests that GBM cells may escape the effect of TTFields over time. The goals of the present study were to identify possible routes by which cancer cells can escape the antimitotic effect of TTFields and to explore ways to overcome such escape mechanisms. Methods: Measurements of cell size before and after 72 hours TTFields application revealed a significant volume increase in 10 cancer cell lines (17% - 101%). A2780 ovarian cancer cultures (cell volume 2.0+0.2 pL) exhibit maximal inhibition by TTFields at 200 kHz. Twenty four hour application of 200 kHz TTFields led to a 70+29% increase in average cell volume (p<0.05). FACS analysis showed that TTFields application to A2780 cells led to a 44% increase in the G2 population due to the antimitotic effect of TTFields. However, the increase in the G2 proportion is not sufficient to explain the increase in cell volume seen after TTFields application. Furthermore, after an additional 24 hours of treatment, the fraction of cells in the G2 population returned to its original percentage (30%), while the increase in cell volume remained high (67+26%). Results: Previous publications demonstrated an inverse relationship exists between cell size and optimal TTFields frequency. Thus an increase in cell size may allow cells to avoid the maximal TTFields effect. To attempt to overcome such cell size escape we decreased the frequency of the TTFields from 200 to 150 kHz after 24 hours treatment to coincide with the increase in cell volume. We found that varying the frequency from 200 to 150 kHz increased the inhibitory effect of TTFields compared to continuous treatment at 200Khz (37+10% and 57+16% decrease in cell count, respectively; p=0.043). Conclusions: This is the first evidence of an escape mechanism from the antimitotic effect of TTFields. The results presented provide a simple way to restore treatment efficacy by varying TTFields frequency in parallel to the change in cell volume.

 

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1. Princess Margaret Cancer Centre (PMCC) Integrated Molecular Profiling in Advanced Cancers Trial (IMPACT) using genotyping and targeted next-generation sequencing (NGS).

Meeting: 2013 ASCO Annual Meeting Abstract No: 11002 First Author: P. L. Bedard
Category: Tumor Biology - New Targets and New Technologies

 

2. The role of the glucocorticoid receptor (GR) in inhibiting chemotherapy-induced apoptosis in high-grade serous ovarian carcinoma (HGS-OvCa).

Meeting: 2013 ASCO Annual Meeting Abstract No: 11101 First Author: E. M. Stringer
Category: Tumor Biology - New Targets and New Technologies

 

3. A community-based program for personalized cancer care using next-generation sequencing (NGS).

Meeting: 2013 ASCO Annual Meeting Abstract No: 11102 First Author: S. Liang
Category: Tumor Biology - New Targets and New Technologies

 

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