Measures of response: RECIST, WHO, and new alternatives

C Carl Jaffe1

  • 1Diagnostic Imaging Branch, Cancer Imaging Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. jaffec1@mail.nih.gov

Insights

Response Evaluation Criteria in Solid Tumors (RECIST) is a standard for assessing tumor size changes. While newer imaging methods offer more detail, RECIST remains vital in clinical trials due to its accessibility and established role.

Area of Science:

  • Oncology
  • Radiology
  • Medical Imaging

Background:

  • Response Evaluation Criteria in Solid Tumors (RECIST) is a standard method for assessing tumor response to therapy since 2000.
  • Increasingly sophisticated imaging technology challenges the simplicity of RECIST.
  • Functionally-based imaging like FDG-PET offers molecular insights, yet CT and MRI remain crucial for anatomical assessment in trials.

Purpose of the Study:

  • To evaluate the current role and future prospects of RECIST in cancer clinical trials.
  • To discuss the potential of advanced image processing for tumor response characterization.
  • To assess the acceptance and utility of alternative quantitative volumetric approaches.

Main Methods:

  • Review of RECIST methodology and its application in clinical trials.
  • Discussion of advancements in imaging technology and image processing.
  • Analysis of proposed alternative quantitative volumetric methods.

Main Results:

  • Anatomically based imaging, including RECIST, continues to play a significant role in clinical trials.
  • Advanced image processing offers opportunities to complement RECIST.
  • Alternative quantitative volumetric methods lack widespread acceptance and proven superiority over RECIST.

Conclusions:

  • RECIST remains a cornerstone in cancer clinical trials due to its availability and established use.
  • Novel imaging techniques and quantitative methods require robust clinical trial designs to demonstrate their added value.
  • Future research must focus on validating new approaches to ensure their clinical utility and regulatory acceptance.

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