Background Detection of S100 beta in serum has been shown to be a significa
nt prognostic market for malignant melanoma in earlier studies. Melanoma in
hibiting activity (MIA) has recently been detected as a new serum marker fo
r malignant melanoma. Materials and Methods: In the present study, serum le
vels of S100 beta protein and MIA were measured over a time period of up to
18 months in 271 serum samples from 65 melanoma patients at different stag
es of disease, during chemotherapy and/or immunotherapy. In addition, 46 se
ra of control patients were analysed The aim of this study was to compare b
oth potential markers. S100 beta was measured using the immunoluminometric
assay LIA-mat(A) Sangtec(R) (Byk Sangtec Diagnostica) with a cut-off level
of 0.12 mu g/l. MLA was determined by the MIA ELISA kit (Roche) using a cut
-off level of 6.5 ng/ml. Results: In 53 patients a direct correlation of S-
100 values and clinical course could be observed (81.5%), whereas in 48 pat
ients MIA-values and clinical course (73.8%) showed an association. S100 be
ta levels were incorrectly elevated in 5 out of 25 sera, "false positive" (
20%) and were in 8 out of 40 sera not elevated despite the detection of met
astases "false negative" (20%). Assessing the MLA levels, 2 out of 25 probe
s were false positive (8%) and 13 out of 40 probes false negative(32.5%). C
onclusion: Our data strongly suggest that S100 and MIA represent serum tumo
r markers that are valuable both in therapy-monitoring and in defection of
tumour progression.