Testing for tumor drug resistance in the age of molecular medicine. A contribution to the Debate Round-Table on phenotypic and genotypic analyses of multidrug resistance (MDR) in clinical hospital practice
T. Efferth, Testing for tumor drug resistance in the age of molecular medicine. A contribution to the Debate Round-Table on phenotypic and genotypic analyses of multidrug resistance (MDR) in clinical hospital practice, LEUKEMIA, 13(10), 1999, pp. 1627-1629
The detection of multidrug resistance (MDR) in clinical hospital practice r
epresents an important strategy to combat clinical tumor drug resistance. P
redicting the response of tumors to cytostatic drugs is of prognostic value
. The 'Debate Round-Table on Phenotypic and Genotypic Analyses of Multidrug
Resistance (MDR) in Clinical Hospital Practice' was launched in 1997 to ad
dress specific questions on this topic. The results published thus far are
a rich source to learn about the promises and pitfalls of methods, eg surro
gate and functional tests and protein or mRNA expression assays as well. In
the present paper, some requirements are discussed for applications of dru
g resistance testing in clinical routine diagnostics. To improve the detect
ion of low-level resistance, established methodologies may be strengthened
with respect to: (1) standardization of sample handling, antibodies, PCR pr
imers, and detection reagents; (2) standardization of protocols and far rea
ching automation in performance and evaluation of results to ensure high qu
ality control criteria. Sophisticated new techniques will feature: (1) high
-throughput analyses for the 'horizontal screening' of single drug resistan
ce genes in large numbers of patient samples at economically fair costs; (2
) 'vertical screening' of a large number of resistance mechanisms operating
upstream or downstream of the actual drug-target interaction sites, in ord
er to detect more complex and multifaceted genotypes and phenotypes of mult
idrug resistance.