Table 4.
Features | MDR+ (n = 63)* | MDR− (n = 28) |
---|---|---|
Shift† | ||
Median | 62 | 24‡ |
Range | 10–99 | 1–98 |
| ||
PSC§ | ||
Median | 86 | 16‡ |
Range | 40–100 | 0–31 |
| ||
Cyclosporine§ | ||
Median | 88 | 8‡ |
Range | 17–100 | 0–33 |
| ||
MRK-16‖ | ||
Median | 65 | 18‡ |
Range | 2–99 | 1–97 |
| ||
KS/D¶ | ||
Median | 0.74 | 0.40‡ |
Range | 0.07–9.8 | 0.05–9.5 |
| ||
MESF# | ||
Median | 6,312 | 3,580** |
Range | 1,625–20,007 | 491–12,612 |
Abbreviations: MDR, multidrug resistance; PSC, valspodar; KS/D, Kolmogorov-Smirnov Statistics; MESF, molecules of equivalent soluble fluorochrome; P-gp, P170-glycoprotein.
≥40% in vitro rhodamine efflux from CD34+ blast cells (see Methods).
Rhodamine fluorescence channel shift, reflecting cellular rhodamine efflux, from baseline (maximal dye uptake and retention) that occurred during a 1-hour incubation of cells at 37°C (to induce dye efflux), expressed as percentage of maximal dye retention.
P = .001.
Percentage of inhibition of in vitro rhodamine efflux from blast cells in the presence of these agents.
Percentage of blast cells immuno-stained with anti-P-gp antibody MRK-16.
Binding of MRK-16 to blast cells relative to background using Kolmogorov-Smirnov statistics, whereby the generated D value reflects the difference between the two binding curves.
MESF (MRK-16 immuno-staining), an indicator of P-gp protein density in the cellular membrane of blast cells.
P = .006.