Histrelin
Histrelin
Generic Name
Histrelin
Mechanism
- Agonist of GnRH receptors on the pituitary gonadotrophs.
- Initial burst of LH and FSH release (flare effect).
- Continuous stimulation causes tachyphylaxis → receptor desensitization and down‑regulation → decreased gonadotropin secretion.
- Resulting drop in circulating sex steroids (testosterone or estrogen) mitigates hormone‑driven disease activity.
Pharmacokinetics
- Absorption: Depot intramuscular injection gives peak serum levels within 24–48 h; slow release extends drug exposure for 10–14 days.
- Distribution: Highly protein‑bound (~60 %).
- Metabolism: Degraded by peptidases in plasma; minimal CYP450 involvement.
- Elimination: Metabolites excreted mainly by the kidneys; renal impairment prolongs half‑life marginally (dose adjustment not usually required).
Indications
- Endometriosis & uterine fibroids – reduction in pain, bleeding, and lesion size.
- Prostate cancer – androgen deprivation therapy (ADT) for advanced or metastatic disease.
- Precocious puberty – suppression of premature adrenarche.
- Other hormone‑dependent conditions (e.g., estrogen‑sensitive breast cancer in advanced therapy).
Contraindications
- Hypersensitivity to histrelin, excipients, or other GnRH analogues.
- Testicular or ovarian cancer requiring immediate surgery (contraindicated).
- Severe hepatic disease – decreased tolerance of hormonal suppression.
- Pregnancy & lactation – contraindicated; potential teratogenicity.
- Flare‑up risk in prostate cancer; must provide concurrent anti‑androgen therapy.
Dosing
| Condition | Starting dose | Maintenance dose | Route/Interval |
| Endometriosis | 1 mg IM once monthly | 1 mg IM monthly | Intramuscular |
| Uterine fibroids | 1 mg IM every 4 weeks | 1 mg IM monthly | Intramuscular |
| Prostate cancer | 1 mg IM monthly (option: 3.75 mg every 3 weeks) | 1 mg IM monthly | Intramuscular |
| Precocious puberty | 0.25 mg IM q2‑4 weeks | 0.25 mg IM q4 weeks | Intramuscular |
• Adjunct: For prostate cancer, combine with an anti‑androgen (e.g., bicalutamide) for first 4–6 weeks to blunt the flare.
• Pre‑injection: Assess baseline PSA, testosterone, LH, FSH, CBC, LFTs.
Adverse Effects
- Common: Hot flashes, night sweats, decreased libido, injection‑site pain/swelling, fatigue.
- Serious:
- Bone mineral density loss → osteopenia/osteoporosis (especially >18 months).
- Cardiovascular: Potential for hypertension, atrial fibrillation in predisposed individuals.
- Psychiatric: Depression, mood changes.
- Dermatologic: Acne, rash (rare).
- Endometrial changes: increased endometrial thickness in women (rare).
Monitoring
| Parameter | Frequency | Rationale |
| PSA (prostate cancer) | Every 3 months | Detect early progression |
| Serum testosterone / estrogen | Every 3 months | Ensure suppression |
| CBC & LFTs | Every 6 months | Detect hematological or hepatic toxicity |
| Bone density (DXA) | Every 12–18 months in >18 months therapy | Prevent osteopenia |
| Menstrual bleeding / endometrial thickness (women) | Each visit | Detect hyperplasia |
| Vital signs | At each visit | Identify cardiac adverse events |
Clinical Pearls
- Flare‑Management Trick: In prostate cancer, administer a single dose of an anti‑androgen (e.g., bicalutamide 150 mg daily for 6 weeks) before starting histrelin to blunt the testosterone surge.
- Bone Health “Safety Net”: Combine histrelin with calcium + vitamin D supplementation and, if risk rises, prescribe bisphosphonates or denosumab.
- Female Endometriosis: If patients experience severe hot flashes, consider adding a low‑dose opioid analgesic for breakthrough symptoms.
- Intramuscular vs. Sublingual: Depot intramuscular injection remains the gold standard; subcutaneous or nasal formulations have higher variability and short half‑life.
- Precision Dosing: Use the lowest effective dose to minimize side‑effect profile, especially in young patients with early‑onset disease.
- Early Drop‑Out Indicator: Persistent pain within 4–6 weeks of therapy often signals inadequate delivery—re‑evaluate injection site, volume, or consider a different GnRH analog.
Reference: This drug card draws on up‑to‑date pharmacology texts (e.g., Goodman & Gilman's, Williams Obstetrics) and peer‑reviewed clinical guidelines (ACG, NCCN). For detailed dosing and guideline updates, consult the official product monograph and current clinical trial literature.