Combination therapy of hormone and cytotoxic agents in advanced breast cancer
β Scribed by David T. Kiang; Daniel H. Frenning; Juliette Gay; Anne I. Goldman; B. J. Kennedy
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 422 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
β¦ Synopsis
The effectiveness of combination therapy with diethylstilbestrol, cyclophosphamide, and 5-fluorouracil (DES + CTx + FU) was compared with DES alone or CTx + FU in 87 postmenopausal women with advanced breast cancer. Therapy was randomized according to the tumor estrogen-receptor (ER) status.
In 30 patients with ER-rich tumors and 35 patients with ER-unknown tumors, combination therapy yielded a higher response rate than DES therapy (87% vs. 64% and 59% vs. 23%, respectively). The pooled data from these two groups of patients suggest that the improved response rate from DES + CTx + FU against DES becomes more apparent in patients with visceral involvement (89% vs. 47%) ( P < 0.025) and that patients treated initially with combination therapy (DES + CTx + FU) appeared to have a longer survival than those treated with sequential therapy (DES + CTx 4 FU) ( P = 0.06). The survival data in 22 patients with receptor-poor tumors were significantly inferior to those with receptor-rich tumors ( P = 0.001). The ER status and presence of visceral metastases are significant factors in the selection of treatment programs.
Cancer 47:452-456, 1981.
RESPONSE RATE of advanced breast cancer
1 treated with chemotherapy has been greater when combination therapies are used. However, the median duration of response from various types of combination chemotherapies has plateaued at nine month^.^ The determination of cytosol estrogen receptors in breast cancer has disclosed the different biologic behaviors among breast cancers and provides a good prediction for their clinical response to endocrine the rap^.^ It is well recognized that endocrine therapy and chemotherapy have different pharmacologic actions and tumoricidal effects in breast cancer. A combination of these two would theoretically not augment their untoward side effects but may yield better tumor control.
π SIMILAR VOLUMES
Sixty-nine patients with advanced breast cancer treated with cytotoxic chemotherapy were randomized to receive concomitantly either norethisterone acetate (progestogen group) or a placebo (placebo group). Objective responses were seen in 53% of patients in the progestogen group and 61% of patients i