TY - JOUR
T1 - The microculture-kinetic (MiCK) assay
T2 - The role of a drug-induced apoptosis assay in drug development and clinical care
AU - Bosserman, Linda
AU - Prendergast, Franklyn
AU - Herbst, Roy
AU - Fleisher, Martin
AU - Salom, Emery
AU - Strickland, Steven
AU - Raptis, Anastasios
AU - Hallquist, Allan
AU - Perree, Mathieu
AU - Rajurkar, Swapnil
AU - Karimi, Misagh
AU - Rogers, Karl
AU - Davidson, Dirk
AU - Willis, Carl
AU - Penalver, Manuel
AU - Homesley, Howard
AU - Burrell, Matthew
AU - Garrett, Audrey
AU - Rutledge, James
AU - Chernick, Michael
AU - Presant, Cary A.
PY - 2012/8/15
Y1 - 2012/8/15
N2 - A drug-induced apoptosis assay, termed the microculture-kinetic (MiCK) assay, has been developed. Blinded clinical trials have shown higher response rates and longer survival in groups of patients with acute myelocytic leukemia and epithelial ovarian cancer who have been treated with drugs that show high apoptosis in the MiCK assay. Unblinded clinical trials in multiple tumor types have shown that the assay will be used frequently by clinicians to determine treatment, and when used, results in higher response rates, longer times to relapse, and longer survivals. Model economic analyses suggest possible cost savings in clinical use based on increased generic drug use and single-agent substitution for combination therapies. Two initial studies with drugs in development are promising. The assay may help reduce costs and speed time to drug approval. Correlative studies with molecular biomarkers are planned. This assay may have a role both in personalized clinical therapy and in more efficient drug development.
AB - A drug-induced apoptosis assay, termed the microculture-kinetic (MiCK) assay, has been developed. Blinded clinical trials have shown higher response rates and longer survival in groups of patients with acute myelocytic leukemia and epithelial ovarian cancer who have been treated with drugs that show high apoptosis in the MiCK assay. Unblinded clinical trials in multiple tumor types have shown that the assay will be used frequently by clinicians to determine treatment, and when used, results in higher response rates, longer times to relapse, and longer survivals. Model economic analyses suggest possible cost savings in clinical use based on increased generic drug use and single-agent substitution for combination therapies. Two initial studies with drugs in development are promising. The assay may help reduce costs and speed time to drug approval. Correlative studies with molecular biomarkers are planned. This assay may have a role both in personalized clinical therapy and in more efficient drug development.
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U2 - 10.1158/0008-5472.CAN-12-0681
DO - 10.1158/0008-5472.CAN-12-0681
M3 - Review article
C2 - 22865459
AN - SCOPUS:84865146617
SN - 0008-5472
VL - 72
SP - 3901
EP - 3905
JO - Cancer Research
JF - Cancer Research
IS - 16
ER -