Table 2

Paclitaxel efflux from histocultures of FaDu xenograft and patient tumors

Tumor TypeInitial CmediumAt 24 h Post-TreatmentAt 72 h Post-TreatmentT1/2,efflux
CmediumCtumorCtumor-to-CmediumRatioRemaining in TumorCmediumCtumorCtumor-to-CmediumRatioRemaining in Tumor
nM nM μM % nM μM % h
Head and neck patient1201.13  ± 0.171.70  ± 0.441560  ± 51454.8  ± 3.11.32  ± 0.141.19  ± 0.50880  ± 30043.3  ± 16.37.45  ± 3.02
1,2007.69  ± 2.554.38  ± 1.99550  ± 8818.7  ± 6.210.9  ± 1.14.17  ± 2.77376  ± 25016.0  ± 5.33.33  ± 2.62
Ovarian patient1201.19  ± 0.240.615  ± 0.149518  ± 6039.8  ± 14.21.60  ± 0.260.520  ± 0.196318  ± 9735.7  ± 18.54.30  ± 0.54
1,20012.8  ± 3.415.13  ± 1.32398  ± 2125.9  ± 8.316.7  ± 2.94.20  ± 1.79245  ± 9919.8  ± 6.65.00  ± 2.93
FaDu xenograft1200.989  ± 0.2283.88  ± 1.274359  ± 12302-a 71.0  ± 6.82-a 1.42  ± 0.183.84  ± 1.042660  ± 4732-a 71.8  ± 1.72-a 6.42  ± 3.51
1,20012.2  ± 1.323.2  ± 5.41800  ± 3002-a 58.6  ± 5.42-a 18.9  ± 5.517.7  ± 3.71010  ± 3392-a 45.0  ± 5.82-a 4.05  ± 1.21

Tumors were incubated with paclitaxel for 24 h. After replacing the drug-containing medium with drug-free medium, the drug concentration remaining in histocultures at 24 and 72 h post-treatment were analyzed to determine the time to reach 50% of the pseudo-steady-state level (T1/2,efflux). The statistical significance of the differences among patient (head and neck and ovarian, n = 6) and FaDu (n = 3) tumors, at equal initial medium concentrations, were analyzed by unpaired t test. Note the different units used for the medium and tumor concentrations. Mean ± S.D. (n = 3). Note that some of the efflux experiments needed different tumors as in the uptake experiments reported in Table 1.

  • 2-a P < .05.