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Figure 1.

An illustration of the algorithm.

(a) The spherical VOIlarge confines the search area. (b) The spherical VOImedium is defined for each pixel in VOIlarge to calculate CVv ( = standard deviation / mean). (c) VOI30 (sphere of 30-mm in diameter) is placed where CVv is smallest. The tumor delineation threshold is defined by the mean and SD within VOI30.

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Figure 2.

A representative case processed with the semi-automated algorithm.

A 150-mm spherical VOIlarge is manually placed to roughly enclose the right lobe of the liver (a, b). For each voxel within VOIlarge, a spherical VOImedium (e.g., 80 mm in diameter) is defined, and mean (c), SD (d), and coefficient of variation of voxel (CVv) (e) within VOImedium are calculated. A 30-mm VOI30 is placed where CVv is minimized (f, g). Image color scales are 0 to 4 SUV for (a–c, f, g), 0 to 1 SUV for (d), and 0 to 0.25 (unitless number) for (e).

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Figure 3.

To evaluate inter-study same-subject reproducibility of the VOI30 location, a cuboid region (red rectangle) was manually created to precisely contain the whole liver.

Location of VOI30 (black circle) was expressed as in the liver coordinate system.

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Table 1.

Mean SUV values within-VOI30 from different methods and physicians.

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Table 2.

Mean ±3 SD values within-VOI30 from different methods and physicians.

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Table 3.

Number of successful results by semi-automated method.

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Figure 4.

A representative case of two studies from the same patient.

(a, b) first study and (c, d) second study. The VOI30's defined using different size of VOImedium (blue: 40 mm, yellow: 60 mm, black: 80 mm, green: 100 mm, red: 120 mm) are drawn on transaxial slices (a, c) and maximum intensity projection images (b, d). The smaller VOImedium located VOI30 further from hepatic portal region with a larger distance between the first and second studies of the same patient than larger VOImedium's did.

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Figure 5.

Euclidian distance between VOI30's from two subsequent studies of the same patient by different VOImedium sizes.

Except the combination of 100-mm and 120-mm, all the combinations showed significant difference (P<0.001) after Holm's correction for multiple comparisons.

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Figure 6.

Bland-Altman plots of metabolic tumor volume.

A1 and A2 represent value from the semi-automated method operated by physician-1 and -2, respectively. M1 and M2 represent manually derived value by physician-1 and -2, respectively. (a) M1 vs. M2, (b) A1 vs. A2, (c) A1 vs. M1, and (d) A2 vs. M2 are compared. Solid lines represent mean difference and dashed lines represent mean ±2SD.

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Figure 7.

Bland-Altman plots of relative change of the metabolic tumor volume (MTV), calculated as [MTVsecond – MTVfirst] / MTVfirst×100 (%).

A1 and A2 represent value from the semi-automated method operated by physician-1 and -2, respectively. M1 and M2 represent manually derived value by physician-1 and -2, respectively. (a) M1 vs. M2, (b) A1 vs. A2, (c) A1 vs. M1, and (d) A2 vs. M2 are compared. Solid lines represent mean difference and dashed lines represent mean ±2SD.

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Figure 8.

Example images of CVv by different VOImedium's (a, d: 40 mm; b, e: 80 mm; c, f: 120 mm).

When 40-mm VOImedium was used (a, d), CVv seemed to be a non-convex function with many local minimums found in peripheral areas of the liver. When 80-mm VOImedium was used (b, e), CVv seemed to be a convex function. The minimum voxel existed in the right lobe of the liver. When 120-mm VOImedium was used (c, f), CVv seemed to be a convex function, but the minimum existed out of the liver. Image color scales are 0 to 0.25 for (a, d), 0 to 0.50 for (b, e), and 0 to 1.00 for (c, f).

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