The ability to precisely describe tumour aggressiveness in human breas
t cancer is inadequate. Current prognostic indicators, although useful
, cannot accurately predict tumour behavior. As a result, multivariate
analyses are required to obtain any significant value from a wide ran
ge of prognostic indicators. Prognostic indications are generally dete
rmined from the primary tumour, but real prognostic value is dependent
upon the activity of potentially metastatic lesions. We present in th
is paper evidence for the use of thymidine kinase, an enzyme indicativ
e of cellular proliferation, as a tumour marker with individual progno
stic value. It has been previously established that thymidine kinase l
evels in both tumours and sera of patients with breast cancer have bee
n shown in clinical studies to be positively correlated with tumour st
age. The monitoring of serial serum samples has also proven to be of p
rognostic value in predicting response to therapy. Measurements of thy
midine kinase levels in primary tumours have demonstrated utility as a
predictor of tumour recurrence. We propose that the development of a
more accurate method of measuring thymidine kinase activity may aid si
gnificantly in the management of breast cancer, while eliminating the
current detection problems of radiolabeling assay systems. This can be
done by the inclusion of an immunologically based detection system.