Postmenopausal patients with oestrogen receptor-positive locally advanced T
-4b, N0-1, M-0 and large operable breast cancers T-2>3 cm, T-3, T-4, N0-1 a
nd M-0 have been treated with 2.5 mg letrozole (12 patients), 10 mg letrozo
le (12 patients), 1 or 10 mg anastrozole (24 patients) and 20 mg tamoxifen
(65 patients), There was no apparent difference in response rate between 2.
5 and 10 mg letrozole. Only 17 patients with anastrozole have so far comple
ted the 3-month treatment period. Median clinical, mammographic and ultraso
und reductions in tumour volumes for patients treated with letrozole were 8
1% (95% confidence interval (CI) 66-88), 77% (95% CI 64-82) and 81% (95% Cl
69-86) respectively and for anastrozole, values were 87% (95% CI 59-97), 7
3% (95% CI 58-82) and 64% (95% CI 52-76) respectively, This compares with a
median reduction in tumour volume for tamoxifen-treated patients as assess
ed by ultrasound of 48% (95% CI 27-48), There were seven complete clinical
responses (CR), sixteen patients who achieved 50% or greater reduction in t
umour volume (PR) and one no change (NC) for letrozole and four CRs, twelve
PRs and one progressive disease for anastrozole. Best radiological respons
es were one CR, twenty PRs and three NCs for letrozole and one CR, fifteen
PRs and one NC for anastrozole. This study has shown that the new aromatase
inhibitors, letrozole and anastrozole, are highly effective agents in the
neoadjuvant setting and they should now be compared with tamoxifen as first
-line treatment in a randomised study.