The accurate detection of low-level disease in patients with cancer is esse
ntial to improve the staging of disease and consequently to define appropri
ate treatment strategies. Most methods currently used for staging are based
on imaging studies and histological and immunocytochemical analysis of tis
sues such as bone marrow aspirates, or antibody assays for marker proteins
secreted into the circulation. These methods have limited sensitivity. Howe
ver, assays for nucleic acid-based markers mag. be valuable tools for the s
ensitive detection, assessment, and monitoring of disease status in asympto
matic cancer patients. Application of these methods may allow the early det
ection of cancer, when the tumour burden is smaller and the disease potenti
ally more curable. The last decade has seen the application of polymerase c
hain reaction (PCR)-based methods to the detection of tumour in a nide vari
ety of compartments, including peripheral blood, bone marrow, lymph nodes,
urine, sputum, faeces, pancreatic juice, and more recently plasma. Molecula
r detection of disease bg PCR has targeted DNA and RNA markers, including m
utations, microsatellites, and tissue-specific gene expression. It is likel
y that these molecular methods will provide important clinical information,
though their current clinical utility remains unclear. The current status
of nucleic acid-based assays for the detection and assessment of disease st
atus in the management of patients with solid tumours is reviewed. Copyrigh
t (C) 2000 John Wiley & Sons, Ltd.