Transcatheter arterial chemoembolisation

Changed by Prashant Mudgal, 22 Jan 2016

Updates to Article Attributes

Body was changed:

Transarterial chemoembolisation therapy (TACE) is a localised method of administrating chemotherapy chemotherapy directly to the liver tumor via a catheter study.

Transarterial embolisation (TAE) (i.e. without a chemotherapy agent added) is also used and there is evidence that this may be just as effective as TACE 1.

Indications

TACE is most commonly used in the treatment of hepatocellular carcinoma (HCC) and selective metastatic disease (most commonly from colorectal carcinoma). It may also be used in cholangiocarcinoma 2.

Procedure

Chemoembolic particles are used to occlude hepatic arterial supply to the tumour with resultant necrosis. There is wide variability in the type of embolisation particles and chemotherapy, as well as timing 1.

Outcomes

TACE has been shown to have a survival benefit over current treatments as well as reducing patient symptoms and preventing tumour growth1,2.

CT is typically used for follow up imaging, with the oily based embolic particles having a distinct high attenuation appearance.

One key advantage is the chemotherapy is targeted locally so reducing the systemic side effects of intravenous chemotherapy.

Response to treatment

Imaging is generally advised after 3-4 weeks, either triple phase CT, dynamic MRI or contrast enhanced USG. The accumulation pattern of the iodized oil and enhancement pattern of the mass is to be observed to evaluate the response to the treatment. The more the accumulation greater the necrosis and the survival. Enhancing areas of tumor are considered as residual viable tumor 5.

There are four types of patterns have been described:

  • type 1
    • homogeneous accumulation of iodized oil in the whole tumour and the surrounding area. This type of accumulation indicates good response to treatment.
  • type 2
    • homogeneous accumulation of iodized oil in the tumour only. This response 
  • type 3
    • irregular accumulation with filling defects. This accumulation represents less than optimal.
  • type 4
    • no accumulation/retention of iodized oil.
  • -<p><strong>Transarterial chemoembolisation therapy</strong> (<strong>TACE</strong>) is a localised method of administrating chemotherapy directly to the liver tumor via a catheter study.</p><p><strong>Transarterial embolisation</strong> (<strong>TAE</strong>) (i.e. without a chemotherapy agent added) is also used and there is evidence that this may be just as effective as TACE <sup>1</sup>. </p><h4>Indications</h4><p>TACE is most commonly used in the treatment of <a href="/articles/hepatocellular-carcinoma">hepatocellular carcinoma</a> (HCC) and selective metastatic disease (most commonly from <a href="/articles/colorectal-carcinoma">colorectal carcinoma</a>). It may also be used in cholangiocarcinoma <sup>2</sup>. </p><h4>Procedure</h4><p>Chemoembolic particles are used to occlude hepatic arterial supply to the tumour with resultant necrosis. There is wide variability in the type of embolisation particles and chemotherapy, as well as timing <sup>1</sup>. </p><h4>Outcomes</h4><p>TACE has been shown to have a survival benefit over current treatments as well as reducing patient symptoms and preventing tumour growth <sup>1,2</sup>.</p><p>CT is typically used for follow up imaging, with the oily based embolic particles having a distinct high attenuation appearance. </p><p>One key advantage is the chemotherapy is targeted locally so reducing the systemic side effects of intravenous chemotherapy.</p>
  • +<p><strong>Transarterial chemoembolisation therapy</strong> (<strong>TACE</strong>) is a localised method of administrating chemotherapy directly to the liver tumor via a catheter study.</p><p><strong>Transarterial embolisation</strong> (<strong>TAE</strong>) (i.e. without a chemotherapy agent added) is also used and there is evidence that this may be just as effective as TACE <sup>1</sup>.</p><h4>Indications</h4><p>TACE is most commonly used in the treatment of <a href="/articles/hepatocellular-carcinoma">hepatocellular carcinoma</a> (HCC) and selective metastatic disease (most commonly from <a href="/articles/colorectal-carcinoma">colorectal carcinoma</a>). It may also be used in cholangiocarcinoma <sup>2</sup>.</p><h4>Procedure</h4><p>Chemoembolic particles are used to occlude hepatic arterial supply to the tumour with resultant necrosis. There is wide variability in the type of embolisation particles and chemotherapy, as well as timing <sup>1</sup>.</p><h4>Outcomes</h4><p>TACE has been shown to have a survival benefit over current treatments as well as reducing patient symptoms and preventing tumour growth <sup>1,2</sup>.</p><p>CT is typically used for follow up imaging, with the oily based embolic particles having a distinct high attenuation appearance.</p><p>One key advantage is the chemotherapy is targeted locally so reducing the systemic side effects of intravenous chemotherapy.</p><h4>Response to treatment</h4><p>Imaging is generally advised after 3-4 weeks, either triple phase CT, dynamic MRI or contrast enhanced USG. The accumulation pattern of the iodized oil and enhancement pattern of the mass is to be observed to evaluate the response to the treatment. The more the accumulation greater the necrosis and the survival. Enhancing areas of tumor are considered as residual viable tumor<sup> 5</sup>.</p><p>There are four types of patterns have been described:</p><ul>
  • +<li>
  • +<strong>type 1</strong> <ul><li>homogeneous accumulation of iodized oil in the whole tumour and the surrounding area. This type of accumulation indicates good response to treatment.</li></ul>
  • +</li>
  • +<li>
  • +<strong>type 2 </strong><ul><li>homogeneous accumulation of iodized oil in the tumour only. This response </li></ul>
  • +</li>
  • +<li>
  • +<strong>type 3</strong><ul><li>irregular accumulation with filling defects. This accumulation represents less than optimal.</li></ul>
  • +</li>
  • +<li>
  • +<strong>type 4</strong><ul><li>no accumulation/retention of iodized oil.</li></ul>
  • +</li>
  • +</ul>

References changed:

  • 5. Kawaguchi T, Ohkawa K, Imanaka K et al. Lipiodol Accumulation and Transarterial Chemoembolization Efficacy for HCC Patients. HGE. 2011;59(113):219-23. <a href="https://doi.org/10.5754/hge11258">doi:10.5754/hge11258</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/22260832">Pubmed</a>
Images Changes:

Image 1 CT (C+ delayed) ( update )

Caption was changed:
Case 1: type 3 pattern

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