Hormonal therapy in patients with breast cancer is based on estrogen blocka
de of tumor cell growth. In postmenopausal patients tamoxifen still represe
nts the hormonal agent of first choice and has shown to induce remission in
patients with metastatic disease, to reduce recurrence, and to improve ove
rall survival in the adjuvant setting. However, side effects such as slight
ly increased incidence of endometrial cancer have stimulated the search for
other substances. Substantial progress in the development of anti-estrogen
s have yielded in substances with different antagonistic/agonistic profils
(Toremifen, Raloxifen, Droloxifen, Idoxifen, ICI 182,780), which are curren
tly tested in phase II and III studies. In the group of the aromatase inhib
itors, which are mostly used in second-line protocols, new compounds are on
the market (Formestan, Anastrazol, Letrozol, Vorozol, Fadrozol) which circ
umvent the main problem of inhibition of the glucocorticoid synthesis of th
e first-generation drugs (glutethimide) by better specificity. These alread
y are widely used in patients with tamoxifen-resistant tumors. Whether thes
e substances can also improve the outcome in first-line therapy is currentl
y under clinical evaluation. An additional therapeutic intervention is the
pharmacological castration (Goserelin), which orginates from the optimistic
result of the surgical castration earlier days. This concept is used in pr
emenopausal patients and currently studied alternatively and in addition to
tamoxifen. In general there is hope to improve efficacy and to reduce side
effects of endocrine treatment with these new compounds in the near future
.