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Medical physics (Lancaster), 2015-06, Vol.42 (6Part6), p.3261-3261
2015
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Autor(en) / Beteiligte
Titel
SU‐E‐I‐83: Error Analysis of Multi‐Modality Image‐Based Volumes of Rodent Solid Tumors Using a Preclinical Multi‐Modality QA Phantom
Ist Teil von
  • Medical physics (Lancaster), 2015-06, Vol.42 (6Part6), p.3261-3261
Ort / Verlag
United States: American Association of Physicists in Medicine
Erscheinungsjahr
2015
Quelle
Wiley Online Library Journals Frontfile Complete
Beschreibungen/Notizen
  • Purpose: In our previous study a preclinical multi‐modality quality assurance (QA) phantom that contains five tumor‐simulating test objects with 2, 4, 7, 10 and 14 mm diameters was developed for accurate tumor size measurement by researchers during cancer drug development and testing. This study analyzed the errors during tumor volume measurement from preclinical magnetic resonance (MR), micro‐computed tomography (micro‐ CT) and ultrasound (US) images acquired in a rodent tumor model using the preclinical multi‐modality QA phantom. Methods: Using preclinical 7‐Tesla MR, US and micro‐CT scanners, images were acquired of subcutaneous SCC4 tumor xenografts in nude rats (3–4 rats per group; 5 groups) along with the QA phantom using the same imaging protocols. After tumors were excised, in‐air micro‐CT imaging was performed to determine reference tumor volume. Volumes measured for the rat tumors and phantom test objects were calculated using formula V = (π/6)*a*b*c where a, b and c are the maximum diameters in three perpendicular dimensions determined by the three imaging modalities. Then linear regression analysis was performed to compare image‐based tumor volumes with the reference tumor volume and known test object volume for the rats and the phantom respectively. Results: The slopes of regression lines for in‐vivo tumor volumes measured by three imaging modalities were 1.021, 1.101 and 0.862 for MRI, micro‐CT and US respectively. For phantom, the slopes were 0.9485, 0.9971 and 0.9734 for MRI, micro‐CT and US respectively. Conclusion: For both animal and phantom studies, random and systematic errors were observed. Random errors were observer‐dependent and systematic errors were mainly due to selected imaging protocols and/or measurement method. In the animal study, there were additional systematic errors attributed to ellipsoidal assumption for tumor shape. The systematic errors measured using the QA phantom need to be taken into account to reduce measurement errors during the animal study.

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