Positron Emission Tomography Response Criteria in Solid Tumors (PERCIST)

Changed by Maxime St-Amant, 21 Jan 2018

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Positron Emission Tomography Response Criteria in Solid Tumors (PERCIST) make use of positron emission tomography (PET) to provide functional information and therebyto help determine tumortumuor viability

Positron Emission Tomography Response Criteria in Solid Tumors, used with 2-[fluorine 18]fluoro-2-deoxy- d-glucose (FDG) positron emission tomography (PET).

The criteria consist of four response categories are: complete metabolic response, partial metabolic response, progressive metabolic disease, and stable metabolic disease. 

Complete Metabolic Response (CMR)

  • Complete

    complete resolution of 18F-FDG uptake within the measurable target lesion

    • so that it is less than mean liver activity and
    • so that it is at the level of surrounding background blood pool activity.
  • Disappearancedisappearance of all other lesions to background blood pool levels.
  • Nono new suspicious 18F-FDG avid lesions.
  • Ifif progression by according to RECIST criteria, must verify with follow up

Partial Metabolic Response (PMR)

  • Reductionreduction of a minimum of 30% in target measurable tumortumour 18F-FDG SUL peak, with absolute drop in SUL of at least 0.8 SUL units.
  • Nono increase >30% of SUL or size in all other lesions
  • Nono new lesions

Stable Metabolic Disease (SMD)

  • Notno CMR, PMR, or Progressiveprogressive metabolic disease (PMD)
  • No new lesions

Progressive Metabolic Disease (PMD)

  • >30% increase in 18F-FDG SUL peak, with >0.8 SUL units increase in tumortumour SUV peak from the baseline scan in pattern typical of tumortumour and not of infection/treatment effect.
  • Oror visible increase in the extent of 18F-FDG tumortumour uptake.
  • Oror new 18F-FDG avid lesions which are typical of cancer and not related to treatment effect orand/or infection.

Acronyms used above

  • SUL = standardized uptake value corrected for lean body mass
  • SULpeak = peak SUL in a spherical 1-cm3 VOI 
  • VOI = volume of interest 
  • -<p>Positron Emission Tomography Response Criteria in Solid Tumors (PERCIST) make use of positron emission tomography to provide functional information and thereby help determine tumor viability. </p><p>Positron Emission Tomography Response Criteria in Solid Tumors, used with 2-[fluorine 18]fluoro-2-deoxy- d-glucose (FDG) positron emission tomography (PET).</p><p>The four response categories are complete metabolic response, partial metabolic response, progressive metabolic disease, and stable metabolic disease. </p><p><strong>Complete Metabolic Response (CMR)</strong></p><ul>
  • -<li>Complete resolution of 18F-FDG uptake within the measurable target lesion so that it is less than mean liver activity and at the level of surrounding background blood pool activity.</li>
  • -<li>Disappearance of all other lesions to background blood pool levels.</li>
  • -<li>No new suspicious 18F-FDG avid lesions.</li>
  • -<li>If progression by RECIST must verify with follow up</li>
  • -</ul><p><strong>Partial Metabolic Response (PMR)</strong></p><ul>
  • -<li>Reduction of a minimum of 30% in target measurable tumor 18F-FDG SUL peak, with absolute drop in SUL of at least 0.8 SUL units.</li>
  • -<li>No increase &gt;30% of SUL or size in all other lesions</li>
  • +<p><strong>Positron Emission Tomography Response Criteria in Solid Tumors</strong> (PERCIST) make use of positron emission tomography (<a title="PET" href="/articles/positron-emission-tomography">PET</a>) to provide functional information to help determine tumuor viability.</p><p>The criteria consist of four categories: complete metabolic response, partial metabolic response, progressive metabolic disease, and stable metabolic disease. </p><h4>Complete Metabolic Response (CMR)</h4><ul>
  • +<li>
  • +<p>complete resolution of 18F-FDG uptake within the measurable target lesion</p>
  • +<ul>
  • +<li>so that it is less than mean liver activity</li>
  • +<li>so that it is at the level of surrounding background blood pool activity</li>
  • +</ul>
  • +</li>
  • +<li>disappearance of all other lesions to background blood pool levels</li>
  • +<li>no new suspicious 18F-FDG avid lesions</li>
  • +<li>if progression according to <a title="RECIST" href="/articles/response-evaluation-criteria-in-solid-tumours">RECIST</a> criteria, must verify with follow up</li>
  • +</ul><h4><strong>Partial Metabolic Response (PMR)</strong></h4><ul>
  • +<li>reduction of a minimum of 30% in target measurable tumour 18F-FDG SUL peak, with absolute drop in SUL of at least 0.8 SUL units.</li>
  • +<li>no increase &gt;30% of SUL or size in all other lesions</li>
  • +<li>no new lesions</li>
  • +</ul><h4>Stable Metabolic Disease (SMD)</h4><ul>
  • +<li>no CMR, PMR, or progressive metabolic disease (PMD)</li>
  • -</ul><p><strong>Stable Metabolic Disease (SMD)</strong></p><ul>
  • -<li>Not CMR, PMR, or Progressive metabolic disease (PMD)</li>
  • -<li>No new lesions</li>
  • -</ul><p><strong>Progressive Metabolic Disease (PMD)</strong></p><ul>
  • -<li>&gt;30% increase in 18F-FDG SUL peak, with &gt;0.8 SUL units increase in tumor SUV peak from the baseline scan in pattern typical of tumor and not of infection/treatment effect.</li>
  • -<li>Or visible increase in the extent of 18F-FDG tumor uptake.</li>
  • -<li>Or new 18F-FDG avid lesions which are typical of cancer and not related to treatment effect or infection.</li>
  • -</ul><p><strong>Acronyms used above</strong></p><ul>
  • +</ul><h4>Progressive Metabolic Disease (PMD)</h4><ul>
  • +<li>&gt;30% increase in 18F-FDG SUL peak, with &gt;0.8 SUL units increase in tumour SUV peak from the baseline scan in pattern typical of tumour and not of infection/treatment effect</li>
  • +<li>
  • +<strong>or</strong> visible increase in the extent of 18F-FDG tumour uptake.</li>
  • +<li>
  • +<strong>or</strong> new 18F-FDG avid lesions typical of cancer and not related to treatment effect and/or infection.</li>
  • +</ul><h4><strong>Acronyms used above</strong></h4><ul>

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