What is TARE?
Trans Arterial Radio Embolization (TARE) is an advanced and minimally invasive
interventional radiology procedure employed in the treatment of liver cancer and liver
metastases. This innovative technique involves the targeted delivery of radioactive
microspheres directly into the blood vessels that supply the tumor. By doing so, TARE
restricts the blood flow to the cancerous cells, delivering a concentrated dose of
radiation precisely to the affected area. This approach not only minimizes damage to
surrounding healthy tissues but also enhances the effectiveness of the treatment.
TARE is particularly valuable for patients who may not be suitable candidates for surgery
or other conventional treatments. As a result, it offers a promising alternative for
individuals facing liver malignancies, contributing to improved outcomes and enhanced
quality of life. This sophisticated procedure is often spearheaded by skilled
Interventional Radiologists, leveraging their expertise to bring about targeted and
impactful interventions in the realm of oncological care.
What to expect?
The treatment process comprises two phases: a pretreatment phase and the actual treatment
phase.
In the initial stage, a pre-SIRT procedure, an exploratory/pretreatment step, will be
conducted. Before this, a comprehensive examination will be conducted. Blood vessels not
leading to the liver will be blocked. Using a local anesthetic, an interventional
radiologist will administer a test dose of a radioactive tracer into the hepatic artery
through a thin tube (catheter) inserted via the femoral vein. Subsequently, a scan at
the nuclear health department will determine if the protein is exclusively absorbed in
the liver.
Once this scan is complete, eligibility for treatment and the appropriate dosage can be
determined. The interventional radiologist will provide further details, and in many
cases, patients can return home by the end of the procedure day.
Moving on to the second phase, the SIRT treatment occurs approximately a week or two
after the pretreatment. This phase follows a similar course as the pretreatment. The
interventional radiologist administers radioactive beads through the hepatic vein toward
the tumor.
These beads become lodged in the blood vessels surrounding and within the tumor, emitting
radiation to destroy the tumor cells and shrink the tumor. Yttrium-90 (Y-90) or
Holmium-166 (Ho-166) radioactive isotopes are commonly used. Since the radiation targets
only the tumor, a higher radiation dose can be employed compared to other treatment
methods, enhancing effectiveness.
It's important to note potential side effects from the treatment. Following the
procedure, an overnight stay at the hospital is required. After the PET-CT scan, the
interventional radiologist will discuss the treatment results with the patient.
What is the condition treated by the TARE procedure?
Trans Arterial Radio Embolization (TARE) is primarily employed in the treatment of liver
conditions, specifically targeting liver cancer and liver metastases. This procedure is
particularly beneficial for individuals who may no longer be viable candidates for
surgery or other conventional treatments.
TARE is commonly used to address primary liver tumors, such as hepatocellular carcinoma
(HCC), and metastatic liver lesions resulting from other cancers, including colorectal
cancer. The procedure involves the precise delivery of radioactive microspheres into the
blood vessels that supply the tumor, thereby restricting blood flow and delivering a
concentrated dose of radiation to the affected area.
This targeted approach minimizes damage to surrounding healthy tissues while maximizing
the therapeutic impact on the cancerous cells. TARE represents a valuable option for
patients facing specific liver malignancies, offering an alternative avenue for
treatment and contributing to improved outcomes in the realm of interventional oncology.
What are the risks and complications?
The primary complication encountered is post-embolization syndrome, affecting
approximately 20 to 70% of patients. Symptoms encom
pass fatigue, mild fever, nausea, vomiting, and abdominal pain. While these symptoms
typically peak in severity during the initial two weeks post-treatment, they may persist
for up to a month.
Less frequently observed complications involve bruising, edema, hepatic impairment, and
infection. In rare instances, individuals may exhibit an allergic reaction to the
contrast agent. The iodine present in the contrast agent can, in extremely uncommon
cases, lead to a kidney response.