P. Sevelda, TAMOXIFEN IN THE TREATMENT OF PATIENTS WITH BREAST-CANCER - RESULTS OF THE LATEST METAANALYSIS OF PROSPECTIVE RANDOMIZED CLINICAL-TRIALS, Gynakologisch-geburtshilfliche Rundschau, 38(2), 1998, pp. 81-84
A meta-analysis of 55 prospective randomized clinical trials including
more than 37,000 patients has analyzed the effectiveness of tamoxifen
in the treatment of breast cancer. Standard treatment consists of 20
mg tamoxifen daily for 5 years in patients with either a positive estr
ogen receptor or a positive progesterone receptor status. This treatme
nt achieves a 50% improvement of the 5-year relapse-free survival and
a 28% improvement of the overall survival. Tamoxifen is effective in l
ymphnode-negative and lymphnode-positive patients as well as in premen
opausal and postmenopausal women. The combination of chemotherapy with
hormonal treatment is even more effective and brings a further improv
ement of survival of 50%. In addition, tamoxifen reduces the number of
contralateral breast cancer cases to 50%, but increase the occurrence
of endometrial cancers from 1.2/1,000 breast cancer patients within 1
0 years to 4.4/1,000 women. In conclusion, tamoxifen 20 mg daily for 5
years is the standard treatment of hormone receptor-positive breast c
ancer patients.