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Title: Evaluation of an Automatic Registration-Based Algorithm for Direct Measurement of Volume Change in Tumors

Journal Article · · International Journal of Radiation Oncology, Biology and Physics
 [1];  [2]; ; ;  [3];  [4];  [5];  [3]
  1. Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI (United States)
  2. Department of Biostatistics, University of Michigan, Ann Arbor, MI (United States)
  3. Department of Radiology, University of Michigan, Ann Arbor, MI (United States)
  4. Department of Biomedical Engineering, Gachon University of Medicine and Science, Incheon (Korea, Republic of)
  5. Department of Internal Medicine (Hematology/Oncology), University of Michigan, Ann Arbor, MI (United States)

Purpose: Assuming that early tumor volume change is a biomarker for response to therapy, accurate quantification of early volume changes could aid in adapting an individual patient's therapy and lead to shorter clinical trials. We investigated an image registration-based approach for tumor volume change quantification that may more reliably detect smaller changes that occur in shorter intervals than can be detected by existing algorithms. Methods and Materials: Variance and bias of the registration-based approach were evaluated using retrospective, in vivo, very-short-interval diffusion magnetic resonance imaging scans where true zero tumor volume change is unequivocally known and synthetic data, respectively. The interval scans were nonlinearly registered using two similarity measures: mutual information (MI) and normalized cross-correlation (NCC). Results: The 95% confidence interval of the percentage volume change error was (-8.93% to 10.49%) for MI-based and (-7.69%, 8.83%) for NCC-based registrations. Linear mixed-effects models demonstrated that error in measuring volume change increased with increase in tumor volume and decreased with the increase in the tumor's normalized mutual information, even when NCC was the similarity measure being optimized during registration. The 95% confidence interval of the relative volume change error for the synthetic examinations with known changes over {+-}80% of reference tumor volume was (-3.02% to 3.86%). Statistically significant bias was not demonstrated. Conclusion: A low-noise, low-bias tumor volume change measurement algorithm using nonlinear registration is described. Errors in change measurement were a function of tumor volume and the normalized mutual information content of the tumor.

OSTI ID:
22058926
Journal Information:
International Journal of Radiation Oncology, Biology and Physics, Vol. 83, Issue 3; Other Information: Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0360-3016
Country of Publication:
United States
Language:
English