Measurement of molecular markers predictive of response to therapy should e
nable more selective and effective utilization of anticancer agents. The pr
edictive value of HER2 remains a complex and inconclusive subject. In metas
tatic breast cancer, HER2-positive, ER-positive patients can show responses
to endocrine treatment, but experience shorter time to progression and sur
vival than HER2-negative patients. In the adjuvant setting, weak, retrospec
tive evidence suggests that tamoxifen is potentially harmful in HER2-positi
ve patients and that there is no benefit from prolonged tamoxifen therapy.
It has not yet been demonstrated conclusively that HER2 positivity increase
s resistance to adjuvant cyclophosphamide, methotrexate, 5-FU (CMF), but th
ere are indications that HER2-positive patients benefit more from adequatel
y dosed anthracyclines than from CMF. The greatest value of HER2 as a predi
ctive marker lies in the prediction of response to therapies that target HE
R2, such as Herceptin (R). Patients with strongly HER2-positive breast canc
er derive significant clinical benefit from single-agent and combined Herce
ptin therapy. HER2 testing has become an integral part of the optimal manag
ement of the breast cancer patient. Best current practice in adjuvant breas
t cancer therapy based on the current knowledge of the potential predictive
power of HER2 constitutes not denying tamoxifen to HER2-positive, ER-posit
ive patients or CMF to HER2-positive patients. Outside of clinical trials,
adequately dosed anthracycline-based chemotherapy is the current preferred
adjuvant treatment option for HER2-positive patients. Copyright (C) 2001 S.
Karger AG, Basel.