The differential staining cytotoxicity (DISC) assay involves in vitro drug
panel testing against patient tumor cells to identify optimal therapy. This
observational study investigated whether DISC assay guided treatment could
improve outcome in patients with chronic lymphocytic leukemia. A cohort of
178 patients were categorized either as sensitive to drugs in vitro and re
ceiving a sensitive drug in vivo, sensitive in vitro but not treated with a
sensitive drug, or having disease resistant to all drugs tested in vitro.
Response and survival for these patient categories were compared using mult
ivariate regression techniques. Patients receiving a sensitive drug, compar
ed with those who though having sensitivity did not, had a higher remission
rate (odds ratio, 6.5; 95% CI, 2.91-14.53) and reduced death rate (hazard
ratio, 0.29; 95% CI, 0.16-0.53). Having adjusted for all known confounding
factors, the results suggest that in vitro drug sensitivity is an important
independent prognostic variable to include in future trials, and that the
DiSC assay may be a cost-effective use of health resources: the estimated i
ncremental cost-effectiveness was $1,470 per life-year gained. A randomized
controlled trial is required to confirm the benefit and estimate reliably
the potential impact of assay-guided choice of therapy.