[Long-term clinical study on TAP-144-SR, an LH-RH agonist depot formulation, in premenopausal patients with advanced or recurrent breast cancer. TAP-144-SR Breast Cancer Study Group]

Gan To Kagaku Ryoho. 1995 Mar;22(4):495-508.
[Article in Japanese]

Abstract

Efficacy and safety of long-term treatment with an LH-RH agonist, TAP-144-SR were studied in premenopausal patients with advanced or recurrent breast cancer. The drug was given sc every 4 week at the dose of 3.75 or 7.5mg. The best objective response rates were 37.0% (17/46) in 3.75mg group, 30.6% (15/49) in 7.5mg group, respectively. The median duration of 12 PR patients in 3.75mg group was 280 (range: 84-830+) days. Serum estradiol level was maintained at < 30pg/ml in most patients given 3.75mg or 7.5mg as scheduled. There was no adverse reactions specific to the longterm administration subsequent to the foregoing 12-week administration study in both dose groups. In conclusion, TAP-144-SR is expected to be one of the first line therapies for patients with premenopausal breast cancer.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • English Abstract
  • Multicenter Study

MeSH terms

  • Adult
  • Breast Neoplasms / blood
  • Breast Neoplasms / drug therapy*
  • Climacteric / drug effects
  • Delayed-Action Preparations
  • Drug Administration Schedule
  • Estradiol / blood
  • Female
  • Gonadotropin-Releasing Hormone / agonists*
  • Humans
  • Injections, Subcutaneous
  • Leuprolide / administration & dosage*
  • Leuprolide / adverse effects
  • Middle Aged
  • Neoplasm Recurrence, Local / drug therapy*
  • Premenopause*

Substances

  • Delayed-Action Preparations
  • Gonadotropin-Releasing Hormone
  • Estradiol
  • Leuprolide