One day new tools might allow physicians to view computed
tomography (CT) images of a tumor and discern its genetic activity,
according to a study that appeared in the May 21 online issue of Nature
Biotechnology. Researchers said the tools could allow physicians to
obtain the molecular details of a specific tumor or disease without
having to do an invasive biopsy procedure.
The new research built on the recent development of DNA microarrays
at Stanford University in California. Microarrays are lab tools that
screen thousands of genes at a time and have proven to be useful for
comparing genetic patterns in diseases, such as cancer, with normal
tissue activity.
Researchers devised a way to connect gene activity seen with
microarrays to imaging patterns (see figure). This would allow
physicians to translate images to gene patterns and, ultimately, to the
outcome of the disease process.
The researchers started with approximately 135 basic tumor
descriptors and then narrowed down the multitude of traits to the 28
most important diagnostic descriptors, matching those imaging features
with a vast stockpile of microarray data generated from human liver
cancer samples.
They then compared features from CT images of liver tumors with the
gene expression patterns. Once they pinpointed the genomic correlates of
the features detected by CT imaging, the researchers found that the
tumor's appearance on CT and its behavior on a molecular level had
a very strong connection.
Out of approximately 7000 genes in the tumors, the research team
was able to consistently associate imaging traits with 75% of the genes.
Researchers acknowledged that they are very far from clinical
applications of these tools. However, the strong connections between the
imaging features and the molecular gene activity data suggest that this
could be a promising research direction.
Inexpensive Ultrasound Scanner Upgrades
A new system will enable health care facilities to inexpensively
upgrade their conventional 2-D ultrasound scanners to provide 3-D
images.
Three-dimensional ultrasound has enabled advances in many areas of
medicine, including fetal research, cardiac imaging and oncology. For
example, 3-D ultrasound can provide important information on the
structure of tumors, their growth pattern and their blood supply.
Although 3-D technology has been available since the 1990s, it
remains prohibitively expensive. Physicians and clinics wishing to
upgrade from 2-D to 3-D technology usually have to invest more than $65
000 in new equipment, according to Fraunhofer Technology Development
Group in Stuttgart, Germany.
Fraunhofer researchers have succeeded in producing a considerably
less expensive solution for physicians that enables conventional 2-D
ultrasound scanners to be upgraded to provide 3-D images for as little
as $540.
The researchers created the system by fitting ultrasound
transducers with inertial sensors that can determine the exact position
and orientation of the probe. Specially developed procedures then allow
reconstruction of a 3-D image from the data.
The inertial sensors are small, inexpensive semiconductor
components that are sensitive to movement in any direction. Such sensors
are normally very imprecise, especially when determining equatorial
coordinates. However, the special procedures developed by the Fraunhofer
engineers enable the exact calculation of spatial coordinates. The
margin of error of the sensors, therefore, could be reduced from around
10 degrees to less than 1 degrees. For the first time, a highly
accurate, low-cost navigation system is available that can be integrated
easily into existing ultrasound scanners.
The new system, which consists of a small device installed with the
necessary software, should be available commercially later this year.
Fraunhofer developed the system in collaboration with MedCom of
Darmstadt, Germany.
NSAIDs May Improve Radiation Therapy
Nonsteroidal anti-inflammatory drugs (NSAIDs) might improve the
cancer-killing ability of both radiation therapy and chemotherapy,
according to 2 new studies.
Because inflammation is thought to play a role in the development
of certain cancers, numerous studies have investigated the role of
NSAIDs such as aspirin and celecoxib in cancer prevention. However, few
studies have evaluated the relative anticancer activity of different
NSAIDs.
In the first study, researchers tested 10 commercially available
NSAIDs against head and neck cancer cells. They found that celecoxib and
sulindac sulfide, sold as Clinoril sulfide, were particularly effective
at killing cancer cells and slowing cancer cell proliferation. Celecoxib
was the most effective, killing up to 60% of head and neck cancer cells
under the study conditions. None of the other 10 NSAIDs in the study,
including aspirin, Aleve and Vioxx, showed effective anticancer
activity.
The study, which appeared in the April 5 online issue of Molecular
Carcinogenesis, also indicated that celecoxib's and sulindac
sulfide's anticancer activity was mediated through cell cycle
inhibition and induction of apoptosis and was not related to the
drugs' anti-inflammatory properties.
In the second study, researchers showed how celecoxib exerts its
anticancer effect by altering protein expression in ways that disrupt
the cell cycle and lead to cell death.
Cells go through 3 phases before they divide: the G1 phase, in
which the cell grows and makes protein; the S phase, in which the cell
makes DNA and replicates its chromosomes; and the G2 phase, in which the
cell prepares for division. The cell cycle also contains several
well-defined checkpoints where the growing cell stops and
"decides" that things are ready to move on to the next stage.
The researchers found that celecoxib specifically kills head and
neck cancer cells in the S phase of the cell cycle, in which the cell
synthesizes new DNA and replicates its genetic material. This is when
cells are most resistant to radiation therapy. Celecoxib's
selective killing of cells in the S phase suggests this class of drugs
could target the radio-resistant cells and use of the drug together with
radiation might provide better tumor control than radiation alone.
The study results also suggest that celecoxib would improve
chemotherapy. Although NSAIDs have adverse side effects, including risk
of cardiovascular and kidney disease, one researcher suggested that the
potential benefits of the drugs outweigh the risks. The second study
appeared in the April 15 issue of Cancer Research.
Imaging Abuse and Fraud Costly to Patients, Industry
Waste, fraud and abuse of diagnostic imaging affect patient safety
and significantly drive overall health care spending, according to a
company that specializes in radiology management.
The growth in radiology procedures has raised concern about the
collective impact of waste, fraud and abuse on the overall cost of care,
as well as patient exposure to radiation, according to MedSolutions, of
Franklin, Tennessee.
The company said that waste is a significant problem in imaging,
with direct-to-consumer marketing and the increasing tendency toward
aggressive surveillance and treatment of incurable diseases helping to
drive the waste.
"Waste is expensive, with unnecessary imaging estimated to
cost the country billions, possibly even as high as $10 billion
annually," said Gregg P. Allen, M.D., chief medical officer of
MedSolutions.
In addition to waste, MedSolutions said fraud and abuse are adding
to the overall imaging cost burden. Dr. Allen pointed out that
self-referral leads to abuse because there is a clear incentive for
physicians to perform imaging studies when the practice will benefit
financially from the study being performed. Additionally, the rapid
increase of imaging equipment in the outpatient setting, the lack of
equipment standardization and the increase in in-office imaging raise
additional opportunities for fraud.
MedSolutions provides radiology expertise to help payers and
Medicaid programs manage their radiology costs.
Shorter Radiation Therapy Regimen Well Tolerated
Women with breast cancer who receive higher doses of radiation with
intensity-modulated radiation therapy (IMRT) each day can reduce their
treatment time by 2 weeks without increasing side effects, according to
a study in the June 1 issue of the International Journal of Radiation
Oncology, Biology and Physics.
Standard radiation therapy for early breast cancer requires daily
treatment for 6 to 7 weeks, which is an inconvenience to many women and
a barrier for breast conservation for some. Researchers wanted to see
how women with breast cancer would tolerate a shorter treatment regimen
with an added radiation boost.
In the study, 75 women underwent IMRT for 4 weeks. The women
received a slightly higher radiation dose to the entire breast while
also receiving a radiation boost to the original lumpectomy site of the
breast. Physicians graded the skin toxicity of each patient, with Grade
0 representing no skin toxicity and Grade 9 representing severe
toxicity.
At the end of the 4-week treatment period, 65% of the women had
Grade 1 skin toxicity and 23% reported a skin toxicity of Grade 2. The
other 12% had Grade 0 toxicity.
In the short-term follow-up at 6 weeks, researchers found that all
toxicity levels had returned to normal, including the women who had
Grade 2 skin toxicity. In addition, the incidence of breast infection
was comparable to previous studies of infection rates after conventional
treatment.
COPYRIGHT 2007 American Society of Radiologic
Technologists Reproduced with permission of the copyright holder. Further reproduction or distribution is prohibited without permission.
Copyright 2007, Gale Group. All rights
reserved. Gale Group is a Thomson Corporation Company.
NOTE: All illustrations and photos have been removed from this article.