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The percentage of necrosis in the maximum tumour section is shown in Figure 4.
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Blood vessel and lymphatic invasion was also explored microscopically, with hematoxylin-eosin and elastic-fiber stained sections of maximum tumour diameter made from paraffin-embedded specimens.
Sections cut through the maximum tumour diameter were selected for IHC evaluation.
Maximum tumour diameters were measured for each primary lung tumour volume.
In mice treated with TMZ, the tumour volumes increased until day 9 reaching maximum tumour sizes, after which decrease of tumour sizes was observed.
For all patients, most PET-based tumour delineation methods could measure the maximum tumour diameter with moderate accuracy.
Figure 1 Mean differences between CT and PET derived maximum tumour diameters and corresponding pathology data.
For the first analysis, the measured maximum tumour diameters were compared with the maximum diameter obtained from pathology.
Therefore, only a comparison with maximum tumour diameter was made rather than with volume.
Difference in maximum tumour diameter between manual CT delineation (A) or various PET-based tumour volume delineation methods (B-C) and pathological size as function of pathological diameter.
Several (semi- automatic PET-basemi- automaticneation methods and manual CT-based delineation were used to assess the maximum tumour diameter.
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