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Pick up to three peptides to see how their mechanisms, studied uses and evidence levels differ. Rows where the entries disagree are marked with a blue edge.

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Comparison
Goserelin

Reproductive & hormonal

Evidence level
Strong evidence
Approval status
Approved drug
Mechanism of action
  1. 1.Binds pituitary GnRH receptors with high affinity.
  2. 2.Continuous stimulation desensitises the gland, so LH and FSH release falls.
  3. 3.Testosterone or oestradiol drops to castrate or postmenopausal levels.
  4. 4.The implant releases a steady dose, avoiding the peaks that would otherwise restore pulsatility.
  5. 5.Suppression is reversible when the implant is stopped.
Studied for
  • Advanced and early prostate cancer
  • Hormone-receptor-positive breast cancer in premenopausal women
  • Endometriosis
  • Endometrial thinning before resection
  • Ovarian suppression in some fertility protocols
Reported effects
  • Castrate testosterone levels within three to four weeks
  • Reduced relapse and improved survival when added to tamoxifen in premenopausal breast cancer trials
  • Substantial reduction in endometriosis pain
  • Reversible menopause-like state with bone loss during treatment
Side effects
  • Hot flushes and sweats
  • Reduced libido
  • Bone mineral density loss
  • Mood changes and fatigue
  • Vaginal dryness
  • Bruising or pain at the implant site
  • Tumour flare at the start
Research protocol

Research context only - prescription medicine. A 3.6 mg implant every 28 days or a 10.8 mg implant every 12 weeks, placed subcutaneously in the abdominal wall, is the licensed pattern; endometriosis treatment is normally limited to six months because of bone density loss, and trials measure hormone suppression and bone mineral density at 6 and 12 months.

Research context only

Evidence justification
Large randomised trials in premenopausal breast cancer (ZEBRA and the Early Breast Cancer Trialists overview) and prostate cancer, with survival and endocrine endpoints.