Academic Radiology
Volume 15, Issue 3 , Pages 334-341, March 2008

Reproducibility of Tumor Volume Measurement at MicroCT Colonography in Living Mice1

  • Benjamin Y. Durkee

      Affiliations

    • Department of Medical Physics, 1400 University Avenue, University of Wisconsin, Madison, WI 53706
  • ,
  • Sarah R. Mudd

      Affiliations

    • Department of Pharmacy, 1400 University Avenue, University of Wisconsin, Madison, WI 53706
  • ,
  • Calista N. Roen

      Affiliations

    • Department of Radiology, 1400 University Avenue, University of Wisconsin, Madison, WI 53706
  • ,
  • Linda Clipson

      Affiliations

    • Department of Oncology, 1400 University Avenue, University of Wisconsin, Madison, WI 53706
  • ,
  • Michael A. Newton

      Affiliations

    • Department of Statistics, 1400 University Avenue, University of Wisconsin, Madison, WI 53706
    • Department of Biostatistics and Medical Informatics, 1400 University Avenue, University of Wisconsin, Madison, WI 53706
    • Paul P. Carbone Comprehensive Cancer Center, 1400 University Avenue, University of Wisconsin, Madison, WI 53706.
  • ,
  • Jamey P. Weichert

      Affiliations

    • Department of Medical Physics, 1400 University Avenue, University of Wisconsin, Madison, WI 53706
    • Department of Radiology, 1400 University Avenue, University of Wisconsin, Madison, WI 53706
    • Paul P. Carbone Comprehensive Cancer Center, 1400 University Avenue, University of Wisconsin, Madison, WI 53706.
  • ,
  • Perry J. Pickhardt, MD

      Affiliations

    • Department of Radiology, 1400 University Avenue, University of Wisconsin, Madison, WI 53706
  • ,
  • Richard B. Halberg

      Affiliations

    • Department of Oncology, 1400 University Avenue, University of Wisconsin, Madison, WI 53706
    • Corresponding Author InformationAddress correspondence to: R.B.H.

Received 20 June 2007; accepted 4 October 2007.

Rationale and Objectives

We sought to demonstrate the viability of microcomputed tomographic colonography (μCTC) as a tool for monitoring tumorigenesis in mouse models of human colorectal cancer during prospective longitudinal studies. The precision and accuracy of volumetric measurements were determined to assess whether changes in tumor volume over time were readily detectable.

Materials and Methods

All animal studies were conducted under the guidelines set forth by the Institutional Animal Care and Use Committee of the American Association for Assessment and Accreditation of Laboratory Animal Care. μCTC was performed on C57BL/6J (B6) mice carrying the Min allele of Apc, ultimately yielding 18 scans. Assessments of scan quality and tumor volume were both performed once per week over 8 weeks.

Results

Scans with a good quality rating had a mean standard deviation in tumor volume measurement of 8%. By contrast, scans with a poor quality rating had a mean standard deviation in tumor volume measurement of 35%. Variables affecting μCTC scan quality in living mice included bowel preparation, motion artifact, and tumor morphology. Tumor volume measurements were highly correlated with tumor weight (r2 = 0.87).

Conclusions

The reproducibility of tumor volume measurement at μCTC in living mice makes prospective longitudinal evaluation of colonic tumor response feasible. For μCTC scans of good quality, a 16% change in tumor volume can be detected at the 95% confidence level.

Key Words: MicroCT virtual colonoscopy, Min mouse, colorectal cancer, tumor volume

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1 Supported by funds to Jamey Weichert from the University of Wisconsin Comprehensive Cancer Center, a R37 grant CA63677 to William F. Dove from the National Cancer Institute, and a NCDDG grant U19 CA113297-03 to Ben Shen from the National Cancer Institute.

PII: S1076-6332(07)00570-3

doi:10.1016/j.acra.2007.10.005

Academic Radiology
Volume 15, Issue 3 , Pages 334-341, March 2008