MADISON, Wis.--(BUSINESS WIRE)--TomoTherapy Incorporated (NASDAQ: TOMO - News) today cited recently published encouraging preliminary results of an ongoing Phase I clinical trial on the use of intensity-modulated (IMRT) and image-guided radiation therapy (IGRT) focusing on the concept of accelerated hypofractionation to overcome tumor repopulation, one of the well-known mechanisms of radiation resistance, using TomoTherapySM for non-small cell lung cancer (NSCLC).
Business Wire - The TomoTherapy Hi-Art system combines CT imaging and radiation delivery for highly-precise cancer treatments that help limit radiation ...
The paper, published in Technology in Cancer Research and Treatment (Technol Cancer Res Treat. 2008 Dec;7(6):441-8.) titled, “Dose Escalated, Hypofractionated Radiotherapy Using Helical Tomotherapy for Inoperable Non-Small Cell Lung Cancer: Preliminary Results of a Risk-Stratified Phase I Dose Escalation Study,” evaluates a study devised to test the safety of escalating the biologically-effective tumor dose via hypofractionated treatment regimens using 25 fractions over five weeks. Traditionally, radiotherapy is delivered over six to seven weeks, or even longer (sometimes up to 10-11 weeks) if dose-escalation is the goal. A downside to dose escalation in this manner is that tumor repopulation occurs during the prolonged delivery time. Shorter dose-escalated schedules have historically been avoided because of the expectation of severe toxicities. The University of Wisconsin (UW) School of Medicine and Public Health investigators hypothesized that the conformal dose-delivery abilities of TomoTherapy, with helical IMRT and IGRT, would permit safe dose-escalation with shorter schedules, thereby limiting accelerated repopulation, and possibly improving tumor control.
According to its authors, the study demonstrates that the use of TomoTherapy technology may allow for higher doses of radiation therapy than are conventionally administered to be delivered over a shorter treatment course, with lower than expected toxicities. Helical TomoTherapy allows for delivery of image-guided, intensity-modulated radiation therapy, permitting conformal delivery of radiotherapy while minimizing the dose delivered to normal tissues.
“The early results of this study suggest that a hypofractionated schedule with dose-escalation can safely be achieved and, although preliminary, the survival data look promising,” said senior author Minesh Mehta, M.D., radiation oncologist and professor of Human Oncology at the UW School of Medicine and Public Health. “Preliminary results suggest that better tumor control and possible survival improvement may be achieved safely with this method, compared retrospectively with traditional radiotherapy techniques.”
Calculations predicting the likelihood of lung toxicity, along with constraints on maximum esophageal and spinal cord dose, were used to help customize the total dose and dose per fraction given to each patient. Doses between 57 and 80.5 Gy were delivered in fraction doses of 2.28-3.22 Gy, representing equivalent doses in 2 Gy fractions of 60-100 Gy.
Promising Preliminary Results:
* For the 46 patients in the study, 80% of whom had stage III NSCLC, overall survival 2 years after treatment was 46.8%. Stage-for-stage, this compares with a 2-year survival rate of 21.5% from a database representing all clinical, surgical-pathologic, and follow-up information for 5,319 patients treated for primary lung cancer. * Higher doses of radiation therapy than are conventionally administered (typically ~60 Gy in 2 Gy fractions) may be delivered safely in a hypofractionated schedule with helical TomoTherapy. Reported lung and esophageal toxicities are lower than expected from previous dose escalation studies using conventional radiotherapy technology. * No patient experienced grade 3 or higher pneumonitis. Grade 2 pneumonitis occurred in only 13% of patients in this study. This illustrates one of the major safety parameters of the study. * No patients experienced grade 3 esophagitis. For those developing esophagitis of grade 1 (24% of patients) or grade 2 (13%) an average weight loss of under 3% occurred. In a University of Michigan dose-escalation study utilizing 3-D radiotherapy, and a non-hypofractionated approach to dose-escalation, grade 1, 2, and 3 esophagitis occurred in 39.5%, 16.5% and 2.7% of patients respectively. The esophageal dose constraints used in the protocol have since been relaxed, given the low incidence of significant esophagitis. * Statistical analysis showed that mean dose to normal lung is a predictor of the rate of lung pneumonitis, but that dose prescribed to the tumor is not. This indicates that the methodology for safe dose prescription based on predicted normal tissue toxicity is valid. The maximum tolerated dose has not been reached and the protocol continues to accrue patients.
Says Rock Mackie, Ph.D., founder and chairman of TomoTherapy and a UW School of Medicine professor, “While it’s still early in the process, we are pleased and encouraged that the results of the study demonstrate that treatment can be delivered in higher doses and in shorter periods of time. This is a promising result which makes us hopeful that there will be improvement in the way non-small cell lung cancer responds to treatment and can be managed moving forward.”
About University of Wisconsin School of Medicine and Public Health
The University of Wisconsin School of Medicine and Public Health is a comprehensive research and teaching facility in Madison Wisconsin, and is home to the UW Paul P. Carbone Comprehensive Cancer Center (UWCCC). Helical tomotherapy was conceived and developed by faculty and staff of the UWCCC and UW School of Medicine and Public Health Departments of Human Oncology and Medical Physics.
About TomoTherapy Incorporated
TomoTherapy Incorporated has developed, markets and sells the TomoTherapy® Hi·Art® treatment system, an advanced radiation therapy system for the treatment of a wide variety of cancers. The Hi·Art treatment system combines integrated CT imaging with conformal radiation therapy to deliver sophisticated radiation treatments with speed and precision while reducing radiation exposure to surrounding healthy tissue. The company’s stock is traded on the NASDAQ Global Select Market under the symbol TOMO. To learn more about TomoTherapy, please visit TomoTherapy.com.
Forward-Looking Statements
Statements in this release regarding future results, expectations, events and other similar matters, including but not limited to statements using the terms “suggest”, “demonstrates” and “may” constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All such forward-looking statements are based on current expectations and are subject to risks and uncertainties. Should any of these risks or uncertainties materialize, or should any of the Company’s assumptions prove incorrect, actual results may differ materially from those included within these forward-looking statements. Accordingly, no undue reliance should be placed on these forward-looking statements, which speak only as of the date made. TomoTherapy assumes no obligation to update or revise the forward-looking statements in this release because of new information, future events or otherwise.
©2009 TomoTherapy Incorporated. All rights reserved. TomoTherapy, Tomo, the TomoTherapy logo and Hi·Art are among trademarks, service marks or registered trademarks of TomoTherapy Incorporated in the United States and other countries.
Photos/Multimedia Gallery Available: http://www.businesswire.com/cgi-bin/mmg.cgi?eid=5936988<=en
MULTIMEDIA AVAILABLE: http://www.businesswire.com/cgi-bin/mmg.cgi?eid=5936988 Contact:
Investor Contact: Stephen C. Hathaway Chief Financial Officer 608.824.2800 shathaway@tomotherapy.com or Media Contact: Kevin O’Malley Manager, Corporate Communications 608.824.3384 komalley@tomotherapy.com
