Supprelin LA
Supprelin LA
Generic Name
Supprelin LA
Mechanism
- GnRH receptor agonist: binds to pituitary GnRH receptors, producing an initial surge in luteinizing hormone (LH) and follicle‑stimulating hormone (FSH).
- Desensitization: continuous stimulation leads to down‑regulation of receptors, resulting in a sustained decrease in LH/FSH secretion.
- Hormonal suppression: ↓ testosterone in males; ↓ estrogen in females, thereby reducing tumor growth or symptomatic estrogen production.
Pharmacokinetics
- Formulation: 3.75 mg or 7.5 mg of leuprolide acetate in a biodegradable polymer for extended release.
- Absorption: subcutaneous (SC) injection; peak serum levels ~24 h post‑injection.
- Distribution: ~15 % protein binding; crosses blood‑brain barrier minimally.
- Metabolism: largely unchanged; metabolized via hydrolysis in plasma.
- Elimination: renal (≈20 %) and hepatic (≈80 %) routes; terminal half‑life 3–4 days; depot release provides effective coverage for 3–6 months.
- Drug interactions: minimal; may potentiate effects of medications causing QT prolongation.
Indications
- Prostate cancer: metastatic or locally advanced hormone‑sensitive disease.
- Gynecologic disorders: endometriosis, uterine fibroids, adenomyosis.
- Endocrinology: precocious puberty, hirsutism (when combined with anti‑androgens).
- Transgender hormone therapy: masculinizing or feminizing protocols in selected cases.
Contraindications
- Hypersensitivity to leuprolide or excipients.
- Pregnancy: contraindicated; risk of fetal testosterone deficiency.
- Severe hepatic impairment: avoid use.
- Known hypersensitivity to GnRH agonists.
- Severe cardiovascular disease: risk of exacerbated ischemia.
- Bone metabolic disorders: baseline bone density testing required.
Dosing
| Indication | Dose | Administration Route | Frequency | Notes |
| Prostate cancer | 3.75 mg SC or 7.5 mg IM | SC (preferred) | 3 months | 3.75 mg for ≤80 kg; 7.5 mg for >80 kg |
| Endometriosis / fibroids | 3.75 mg SC | SC | 3 months | May repeat up to 12 months |
| Precocious puberty | 0.3 mg/kg SC | SC | Every 4 weeks | Adjust to body weight |
| Transgender therapy | 7.5 mg SC | SC | 3 months | Combine with anti‑androgen or estrogen |
• Injection technique: Rotate sites, use 1–2 cm depth; observe for pain, erythema, or hematoma.
• Premedication: Not routinely required; antihistamine may be used if history of injection reaction.
Adverse Effects
| Category | Common (≥10 %) | Serious (≤1 %) |
| Endocrine | Hot flashes, night sweats, decreased libido, erectile dysfunction | Acute hypogonadism symptoms (e.g., severe mood changes) |
| Metabolic | Weight gain, fluid retention, hyperglycemia | Cardiovascular events (myocardial infarction, stroke) |
| Bone | Mild bone mineral loss | Osteoporotic fracture |
| Injection site | Pain, erythema, induration, local pruritus | Abscess, granuloma |
| Others | Headache, dizziness, fatigue | Seizure, severe hypotension |
Monitoring
- Seizures: rare but reported; monitor neurologic status.
- Cardiac arrhythmias: consider baseline ECG if at risk.
- Bone fractures: high risk in elderly or long‑term use.
Clinical Pearls
- “Hot‑flash first aid”: co‑prescribe low‑dose NSAIDs or gabapentin; avoid hot‑flash‑inducing triggers (caffeine, alcohol).
- Bone health: co‑treat with bisphosphonates or denosumab if baseline T‑score ≤ −1.5 or if >5 years of therapy.
- Weight‑based dosing: 3.75 mg SC for patients < 80 kg; 7.5 mg for heavier patients—skipping the weight adjustment can lead to suboptimal suppression.
- Avoid “bolus” injection: use the slow‑release polymer; a single 3.75 mg SC dose yields ~90 % suppression for 3 months.
- Transgender protocol: use 7.5 mg SC every 3 months; monitor testosterone and estrogen levels; consider adding aromatase inhibitor if estradiol remains high.
- Injection site rotation: SC injections into the abdomen, thigh, or buttock; avoid the same site every visit to minimize scar tissue and local pain.
- Pregnancy test: mandatory before every cycle; patient education on contraception during therapy.
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• Key Takeaway: Supprelin LA provides reliable, long‑acting hormonal suppression with a favorable safety profile when properly monitored. Use dose‑adjusted SC injections, proactive bone protection, and patient education to maximize efficacy and minimize adverse events.