The predictive value of the oncogene product ErbB-2 for chemosensitivity of
tumors is still unclear. We therefore correlated the in vitro chemosensiti
vity of breast cancer specimens from 125 patients with the respective expre
ssion levels of ErbB-2. Twenty-six percent of the patients were premenopaus
al Chemosensitivity was tested with the adenosine triphosphate cell viabili
ty assay and ErbB-2 content was assessed in the same specimens by ELISA. Wi
th the cut-off value used 34 % of the patients had turners with positive Er
bB-2 levels. The mean ErbB-2 amount of positive tumors was 388 U/mg +/- 254
and of negative tumors 65 U/mg +/- 36. The mean survival fractions (SF) in
the chemosensitivity assay at 0.25 peak plasma concentration (PPC) of a co
mbination of cyclophosphamide, methotrexate and 5-fluorouracil (CMF) were n
ot significantly, different for. ErbB-2-positive and for ErbB-2-negative tu
mors (0.68 and 0.65, respectively (p = 0.6)). The median SF for positive tu
mors was 0.68 and for negative tumors 0.62, respectively. Similarly, at fou
r times the PPC of CMF no significant differences in SF of ErB-2-positive a
nd -negative specimens were found (p = 0.8). Comparison of the median of Er
bB-2-protein content of CMF-sensitive tumors with that of CMF-resistant tum
ors also yielded no significant difference. Taken together; no significant
association between in vitro CMF-chemosensitivity and expression levels of
ErbB-2 in tumors of patients with primary chemotherapy naive breast cancer
could be determined.