"A huge European trial has shown that the 70-gene assay MammaPrint can identify patients with early breast cancer who can safely skip adjuvant chemotherapy, even if they have clinical characteristics suggesting they are at high risk.
(Generic versions may still be available.)
TESLAC (testolactone) is recommended as adjunctive therapy in the palliative treatment of advanced or disseminated breast cancer in postmenopausal women when hormonal therapy is indicated. It may also be used in women who were diagnosed as having had disseminated breast carcinoma when premenopausal, in whom ovarian function has been subsequently terminated.
TESLAC (testolactone) was found to be effective in approximately 15 percent of patients with advanced or disseminated mammary cancer evaluated according to the following criteria: 1) those with a measurable decrease in size of all demonstrable tumor masses; 2) those in whom more than 50 percent of non-osseous lesions decreased in size although all bone lesions remained static; and 3) those in whom more than 50 percent of total lesions improved while the remainder were static.
DOSAGE AND ADMINISTRATION
The recommended oral dose is 250 mg qid.
In order to evaluate the response, therapy with testolactone should be continued for a minimum of three months unless there is active progression of the disease.
TESLAC® (testolactone tablets, USP), 50 mg/tablet: bottles of 100 (NDC 0003-0690-50). Each round, white, biconvex tablet is imprinted with the identification number 690.
Store at controlled room temperature 25°C (77°F).
Bristol-Myers Squibb Company, Princeton, NJ 08543 USA. Made in Australia. Revised May 2004This monograph has been modified to include the generic and brand name in many instances.
Last reviewed on RxList: 6/30/2009
Additional Teslac Information
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
Find support and advances in treatment.