Table 1.
Study design of treatment groups, cyclophosphamide and temsirolimus, monitored with FDG-PET and FLT-PET on d0 (before treatment), d2, d4, d7, d9 and d14. Tumor volumes (Volcalip) were measured with a caliper. Immunohistochemical (IHC) and DNA FACS studies were performed on corresponding days following therapy.
Cyclophosphamide (n=17) | d0 | d2 | d4 | d7 | d9 | d14 |
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FDG-PET + caliper (n=4) | X | X | X | X | X | X |
FLT-PET + caliper (n=5) | X | X | X | X | X | X |
IHC and DNA FACS (n=8) † | n=2 | n=2° | n=2 | n=2 | * | |
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Temsirolimus (n=17) | d0 | d2 | d4 | d7 | d9 | d14 |
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FDG-PET + caliper (n=5) | X | X | X | X | X | X |
FLT-PET + caliper (n=4) | X | X | X | X | X | X |
IHC and DNA FACS (n=8) † | n=2 | n=2° | n=2 | n=2 | * | |
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Control (n=2) | d0 | |||||
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IHC and DNA FACS (n=2) | n=2 |
In total 8 mice were sacrificed for analysis on d2,4,7,9 (2 mice per time point);
tumors were dissected from mice following their final scan on d14;
Only IHC no DNA FACS