Imagine destroying a tumor in 6
minutes with a small needle electrode
placed through the skin into
a tumor deep in the human body-the
patient is cured after spending only a
few hours in the hospital and leaves
with just a small bandage. This may
sound like science fiction, but it is
reality in many medical centers around
the world.
It seems like yesterday that I was a
resident rotating through Massachusetts
General Hospital, helping Dan
Rosenthal treat an osteoid osteoma by
radiofrequency (RF) ablation. That
defining event, which took place 14
years ago, was my first exposure to
image-guided tumor ablation; that
seminal work[1] encouraged me and
others to become involved in this burgeoning
field of medicine. As guest
editor of this supplement to ONCOLOGY
devoted to image-guided ablation,
I would like not only to share my
thoughts on the past and present, but
also to shed some light on patient
management and follow-up. I thank
my fellow contributors to this supplement
for their concise and clinically
relevant overviews of the most important
areas of image-guided tumor
ablation. I found them balanced and
extremely well written.
Over the past decade we have seen
a continued expansion of clinical applications
for ablative techniques
through single-center trials and several
multicenter trials designed to rigorously
document safety and efficacy.
The proliferation of ablation technology
and its dissemination into the
treatment of various solid tumors[2]
is the reason for this update, which will
be invaluable for those interested in
introducing this new technology into
their radiology practices as well as those
who are already using it. The short
reviews highlight the current knowledge
of image-guided tumor ablation
in liver, kidney, bone, and lung and
illustrate its use with pertinent clinical
examples. We understand that some
areas of utilization are further along in
widespread implementation than others.
For those areas that are less well
researched, we provide provocative
viewpoints for future expansion.
History and Development
The concept of killing a tumor in
situ without ionizing radiation or surgery
is not new, as the quotation from
Hippocrates attests. Previously, direct
visualization was necessary, as in the
pouring of liquid nitrogen into the
cavity created by a giant cell tumor of
bone.[2] The advent of cross-sectional
imaging with ultrasound or CT enabled
physicians to precisely and
directly place needles percutaneously
into solid tumors in almost all regions
of the human body. The procedure
was initially performed for diagnosis
by needle biopsy, but direct therapeutic
intervention closely followed.
In 1986, Livraghi and colleagues
described the direct injection of chemotherapy
into tumors of the liver,
pancreas, pelvis, and lung under crosssectional
imaging guidance.[3] This
work was shortly followed by the direct
injection of absolute ethanol.[4]
Heat-based ablative technologies had
been available for decades and were
initially applied to the trigeminal ganglion
for treating patients with trigeminal
neuralgia.[5] This same
technology was then applied to
bone[6] and eventually led to the treatment
of osteoid osteomas.[1] As the
RF technology improved, newer devices[
7,8] allowed the destruction of
larger volumes of tissue, opening up
new applications that were quickly
applied to liver tumors. With the creation
of cryoprobe technology in the
early 1960s[9] and refinements in the
late 1970s and 1980s, surgeons and
radiologists could place probes directly
into liver tumors in the operative
setting, using ultrasound guidance.
Newer percutaneous cryoprobes
developed over the past decade have
enabled additional clinical applications,
including treatment of prostate
cancer.[10] Other heat-based ablative
technologies also being used to treat
tumors under image guidance, such
as laser and microwave, show considerable
promise. The ultimate goal of
these techniques is to provide excellent
local control rates with fast treatment
times at reasonable cost.
Head-to-head comparisons in the literature
are thus far lacking, and this
presents a fertile area for image-guided
interventional research.
Patient Selection
Appropriate patient selection is essential
to the success of these new
technologies. Similar oncologic principles
apply to ablation as to radiation
therapy and surgery. Removal or destruction
of a local tumor makes sense
when tumor staging suggests localized
disease or when symptom control
or palliation is the goal. Choosing
the appropriate patient also means
choosing the appropriate tumor and
taking the tumor biology into consideration.
Rapidly growing tumors with
rapid dissemination characteristics are
poor candidates for local therapy.
Many patients have comorbid medical
conditions that make traditional
oncologic treatments such as surgery,
radiation, and chemotherapy inappropriate
for them. Treating these patients
makes sense if tumor control is
likely to improve their quality or quantity
of life. Implementing local ablative
therapy does not make sense if
the patient is likely to succumb to an
underlying medical condition.
As cancer treatment is a relatively
new area for most radiologists, conferring
with a team of subspecialists
at the tumor board level is an excellent
means of acquiring the knowledge
and credibility of the other
treating physicians. The team approach
becomes increasingly important
for patients who are candidates
for multimodal therapy, given the systemic
nature of many cancers and the
known synergy of ablative techniques
with chemotherapy and radiation.
Imaging Evaluation
Since ablative therapy is not extirpative,
identifying residual or recurrent
disease against the background
of treatment effects can be difficult
in the early posttreatment period.
Positron emission tomography and
contrast CT/MRI may identify areas
of persistent metabolically active tissue
or tumor neovascularity. The precise
timing and sensitivity of these
techniques has not been defined, but
suffice to say that growth in size beyond
the postablation baseline examination
is more than likely tumor
growth, and new metabolically active
areas with qualitative and quantitative
assessment in the neoplastic
range are also likely evidence of progression.
Current scientific study on
the most appropriate modality and
timing of utilization is not yet conclusive.
Ongoing multicenter trials
have incorporated imaging evaluation
as part of the scientific design in the
hopes of answering these important
questions. As with many patient examinations,
definitive answers in
equivocal cases can be obtained by
biopsy evaluation or additional follow-
up over time.
Conclusion
Because the field of image-guided
tumor ablation is young, many questions
remain unanswered. Early results
are very encouraging, however,
and the future scientific progress in
technology and clinical trials will surely
lead to its continued success and
implementation.
