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Research ArticleCLINICAL INVESTIGATIONS

Early Prediction of Response to Chemotherapy and Survival in Malignant Pleural Mesothelioma Using a Novel Semiautomated 3-Dimensional Volume-Based Analysis of Serial 18F-FDG PET Scans

Roslyn J. Francis, Michael J. Byrne, Agatha A. van der Schaaf, Jan A. Boucek, Anna K. Nowak, Michael Phillips, Richard Price, Andrew P. Patrikeos, A. William Musk and Michael J. Millward
Journal of Nuclear Medicine September 2007, 48 (9) 1449-1458; DOI: https://doi.org/10.2967/jnumed.107.042333
Roslyn J. Francis
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Michael J. Byrne
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Agatha A. van der Schaaf
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Jan A. Boucek
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Anna K. Nowak
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Michael Phillips
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Richard Price
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Andrew P. Patrikeos
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A. William Musk
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Michael J. Millward
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  • FIGURE 1. 
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    FIGURE 1. 

    Coronal slices of an 18F-FDG PET scan of a patient with mesothelioma demonstrating contiguous involvement of the right pleural surface, including infiltration of the oblique fissure. There is additional subcarinal, precarinal, right paratracheal, and right hilar lymph node involvement.

  • FIGURE 2. 
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    FIGURE 2. 

    Representative CT transaxial slices of a patient with mesothelioma (A) before chemotherapy and (B) after chemotherapy. Measurements according to modified RECIST criteria have been applied. The patient had a radiological partial response after 1 cycle of chemotherapy. The challenge of defining a measurement site to determine response is demonstrated. Representative 18F-FDG PET transverse, sagittal, and coronal slices in the same patient (C) before chemotherapy and (D) after 1 cycle of chemotherapy. A significant reduction in intensity and extent of 18F-FDG uptake in the left pleural cavity is demonstrated. The response is more clearly visualized on the 18F-FDG PET imaging, and the degree of change compared with baseline in the patient was greater (TGV fell to 11% of baseline on the postchemotherapy scan, compared with a fall to 63% of baseline on CT measurements).

  • FIGURE 3. 
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    FIGURE 3. 

    Representative 18F-FDG PET coronal slices in a patient with left pleural mesothelioma (A) before chemotherapy and (B) after 1 cycle of chemotherapy, demonstrating reduction in the extent and intensity of 18F-FDG activity. The region generated by the semiautomated region-growing algorithm is shown on the coronal slice (C) before chemotherapy and (D) after chemotherapy. (A–D) illustrate one representative coronal slice both before and after chemotherapy; however, in practice the region is grown in 3 dimensions to define an overall volume of interest (VOI). (E) Histogram of the SUV voxel values of the VOI generated by the region-growing algorithm in this patient before chemotherapy (red line) and after chemotherapy (green line). The histogram demonstrates both a reduction in the numerical SUV values and in the overall volume of metabolically active tumor. The TGV fell to 30% of the prechemotherapy value.

  • FIGURE 4. 
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    FIGURE 4. 

    18F-FDG PET TGV and SUVmax percentage response values compared with CT response values in the 7 patients with CT-defined PR (A) and 13 patients with CT-defined SD after 1 cycle of chemotherapy (B). All values are expressed as a percentage of the baseline value. The solid line represents the 70% value used in CT to define a PR.

  • FIGURE 5. 
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    FIGURE 5. 

    Kaplan–Meier survival curves illustrate the relationship between the degrees of reduction in TGV compared with baseline and survival. TGV <60% represents a reduction in TGV after 1 cycle of chemotherapy to less than 60% of the baseline value. TGV 60%–85% represents a reduction to 60%–85% of the baseline value. TGV >85% includes patients whose TGV after chemotherapy was 85% or greater than the baseline value and patients whose TGV increased after chemotherapy.

Tables

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    TABLE 1

    Patient Demographics and 18F-FDG PET Response of the 23 Patients in the Study, with Patients Grouped According to CT Response Attained After 1 Cycle of Chemotherapy

    CT response
    Patient demographicsPRSDnm
    No. of patients (%)7 (30)13 (57)3 (13)
    Age (y)
     Median676467
     Range61–7154–7552–73
    Male sex (%)5 (71)12 (92)3 (100)
    Baseline TGV (SUV·mL)
     Median3,3725,056844*
     Range278–16,101897–15,810834–853
    Baseline SUVmax (SUV)
     Median12.212.86.4*
     Range5.4–13.95.5–18.15.3–7.5
    TGV1/TGV0 (%)†
     Median307192*
     Range11–718–11383–101
    SUVmax1/SUVmax0 (%)‡
     Median598098*
     Range39–7240–11192–103
    • ↵* A TGV or SUVmax measurement could be obtained in only 2 of 3 patients. Therefore, median and range are derived from only 2 data points.

    • ↵† TGV after 1 cycle of chemotherapy divided by baseline TGV value and expressed as a percentage.

    • ↵‡ SUVmax after 1 cycle of chemotherapy divided by baseline SUVmax value and expressed as a percentage.

    • PR = partial response; SD = stable disease; nm = not measurable.

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    TABLE 2

    Baseline and After 1 Cycle of Chemotherapy, TGV and SUVmax Values for All Patients, Grouped According to CT Response

    StatusSexAge (y)TGV0TGV1TGV1/TGV0 (%)SUV0SUV1SUV1/SUV0 (%)Survival (mo)
    CT PR
    1M69278138505.64.07123.7†
    2M*671,1001771613.97.5548.0
    3F6116,1014,8143013.27.55718.7†
    4M697,2051,1301611.58.37211.5
    5M719,8401,0891113.15.13910.3†
    6M663,3722,0336012.27.4613.9†
    7F65549390715.43.2594.4†
    CT SD
    8M689,17710,41211312.812.2954.9
    9M554,7015,0121075.54.5821.4
    10M635,1395,057989.08.7976.9
    11M683,0482,2687418.114.0779.5
    12M545,6313,762679.06.87617.6
    13M644,3982,8626513.06.8525.9
    14M*6015,80911,1047013.611.18214.5†
    15M553,10426589.33.74012.4†
    16F711,4131,47010413.210.6809.9
    17M745,4843,4406310.910.2946.2†
    18M659,6357,7548013.010.4805.9
    19M758974234717.87.5422.9†
    20M545,0563,5747110.011.11112.5†
    CT nonmeasurable
    21M528538611015.34.9927.5
    22M73834689837.57.710312.2
    23M67n/en/en/en/en/en/e8.4†
    • ↵* Previous talc pleurodesis.

    • ↵† Survival at time of censorship (alive).

    • TGV0 = TGV at baseline (before chemotherapy); TGV1 = TGV after 1 cycle of chemotherapy; TGV1/TGV0 (%) = TGV after 1 cycle of chemotherapy divided by baseline TGV value and expressed as a percentage; SUV0 = SUVmax at baseline (before chemotherapy); SUV1 =SUVmax after 1 cycle of chemotherapy; SUV1/SUV0 (%) = SUVmax after 1 cycle of chemotherapy divided by baseline SUVmax value and expressed as a percentage; n/e =not evaluable, as a VOI could not be generated on PET images.

    • View popup
    TABLE 3

    Cox Proportional Regression Analysis of Relationship Between Change in CT, SUVmax, and TGV after 1 Cycle of Chemotherapy and Survival

    10% changeHazard ratio95% CIP value
    CT0.710.21–1.070.131
    SUVmax0.650.12 –1.050.097
    TGV0.640.26–0.940.015
    • The boldface P value 0.015 indicates the value is statistically significant.

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Journal of Nuclear Medicine: 48 (9)
Journal of Nuclear Medicine
Vol. 48, Issue 9
September 2007
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Early Prediction of Response to Chemotherapy and Survival in Malignant Pleural Mesothelioma Using a Novel Semiautomated 3-Dimensional Volume-Based Analysis of Serial 18F-FDG PET Scans
Roslyn J. Francis, Michael J. Byrne, Agatha A. van der Schaaf, Jan A. Boucek, Anna K. Nowak, Michael Phillips, Richard Price, Andrew P. Patrikeos, A. William Musk, Michael J. Millward
Journal of Nuclear Medicine Sep 2007, 48 (9) 1449-1458; DOI: 10.2967/jnumed.107.042333

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Early Prediction of Response to Chemotherapy and Survival in Malignant Pleural Mesothelioma Using a Novel Semiautomated 3-Dimensional Volume-Based Analysis of Serial 18F-FDG PET Scans
Roslyn J. Francis, Michael J. Byrne, Agatha A. van der Schaaf, Jan A. Boucek, Anna K. Nowak, Michael Phillips, Richard Price, Andrew P. Patrikeos, A. William Musk, Michael J. Millward
Journal of Nuclear Medicine Sep 2007, 48 (9) 1449-1458; DOI: 10.2967/jnumed.107.042333
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