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. 2011 Dec 15;2(1):110–121.

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

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 *

Temsirolimus (n=17) d0 d2 d4 d7 d9 d14

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 *

Control (n=2) d0          

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