What is the use and administration of Decapeptyl (triptorelin) in treating conditions such as prostate cancer, precocious puberty, and uterine fibroids?

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Decapeptyl (Triptorelin): Clinical Uses and Administration

Primary Indications

Decapeptyl (triptorelin) is a GnRH agonist indicated for advanced prostate cancer, central precocious puberty, and off-label for uterine fibroids, with multiple formulations allowing flexible dosing intervals from 1 to 6 months. 1


Prostate Cancer

Standard Treatment Approach

  • Triptorelin is equivalent to surgical castration (bilateral orchiectomy) and other LHRH agonists for metastatic hormone-naive prostate cancer. 2
  • Available formulations include 3.75 mg (monthly), 11.25 mg (3-month), and 22.5 mg (6-month) administered intramuscularly. 2, 1
  • The 6-month formulation achieves castrate testosterone levels (<50 ng/dL) in 97.5% of patients by day 29 and maintains suppression in 93% through 12 months. 3

Administration Protocol

  • Antiandrogen therapy (flutamide, bicalutamide, or nilutamide) must be initiated 1 week before or coadministered with the first LHRH agonist injection and continued for at least 7 days to prevent testosterone flare in patients with metastatic disease or those at risk for spinal cord compression. 2
  • For patients at high risk of immediate complications from metastases (e.g., spinal cord compression), avoid LHRH agonists initially; use bilateral orchiectomy, antiandrogen monotherapy, or LHRH antagonist instead. 2
  • Testosterone levels increase transiently during the first week, peaking on days 2-4, before declining to castrate levels by weeks 3-4. 1

Monitoring Requirements

  • Measure serum testosterone at baseline and every 4 weeks initially to confirm castration (<50 ng/dL). 1, 3
  • Monitor PSA at baseline, then at 12-week intervals. 3
  • Continue androgen deprivation therapy lifelong once initiated, even after progression to castration-resistant disease. 2

Critical Warnings

  • Tumor flare phenomenon occurs in the first 2-3 weeks, potentially causing worsening bone pain, urinary obstruction, hematuria, or spinal cord compression with paralysis. 2, 1
  • Monitor for cardiovascular events (myocardial infarction, stroke, sudden cardiac death), which have increased risk with GnRH agonists. 1
  • Check baseline and periodic ECGs in patients with congenital long QT syndrome, heart failure, or electrolyte abnormalities, as triptorelin may prolong QT/QTc interval. 1
  • Screen for metabolic syndrome: monitor lipids, glucose, and HbA1c periodically, as androgen deprivation increases risk of diabetes and cardiovascular disease. 1

Central Precocious Puberty (CPP)

Diagnostic Criteria

  • CPP is defined as onset of secondary sexual characteristics before age 8 in girls or age 9 in boys, with bone age advancement ≥1 year over chronological age. 4
  • Confirm diagnosis with GnRH stimulation test showing pubertal LH response (stimulated LH >5 IU/L). 4

Treatment Protocol

  • Triptorelin 22.5 mg (6-month formulation) administered intramuscularly every 24 weeks is effective and safe for CPP. 4
  • Alternative shorter-acting formulations (1-month or 3-month) are also available but require more frequent injections. 5, 4
  • Treatment achieves LH suppression to prepubertal levels (stimulated LH ≤5 IU/L) in 93.2% of patients at 6 months and 97.7% at 12 months. 4

Monitoring Efficacy

  • Urinary FSH from nocturnal spontaneous urine (≤5.24 IU/L), diurnal stimulated urine (≤6.94 IU/L), or nocturnal stimulated urine (≤5.78 IU/L) measured by immunochemiluminometric assay provides a non-invasive method to assess treatment efficacy. 6
  • Perform triptorelin stimulation test (100 μg) at 3-month intervals to confirm adequate suppression. 6
  • Monitor bone age, growth velocity, and pubertal staging at each visit. 4

Adverse Effects

  • Hot flushes are the most common side effect (71.7% of patients). 3
  • Local injection site reactions occur in 3.6% of patients. 1
  • No unexpected adverse events have been reported in pediatric populations. 4

Uterine Fibroids (Off-Label Use)

Rationale and Duration

  • GnRH agonists including triptorelin induce a hypoestrogenic state, causing fibroid shrinkage and symptom relief. 5
  • Treatment duration should be limited to 3-6 months due to bone density loss from prolonged hypoestrogenism. 5
  • Typically used as preoperative therapy to reduce fibroid size and vascularity before myomectomy or hysterectomy. 5

Formulation Selection

  • Use 3.75 mg monthly or 11.25 mg 3-month formulations for short-term preoperative therapy. 2
  • The 6-month formulation is less practical for this indication given the limited treatment duration. 5

Practical Administration Details

Injection Technique

  • Reconstitute with 2 mL sterile water for injection immediately before use. 1
  • Administer deep intramuscular injection into the gluteal muscle. 1, 7
  • Subcutaneous administration is equally effective and well-tolerated for the depot formulation. 7

Cost Considerations

  • Triptorelin (Trelstar) costs approximately $1,696 per 6 months across all formulations (3.75 mg monthly, 11.25 mg quarterly, or 22.5 mg biannually), with 340B pricing ranging from $97-$127 per dose. 2
  • The 6-month formulation reduces injection frequency, potentially improving compliance and patient comfort. 5, 3

Common Pitfalls to Avoid

  • Failing to provide antiandrogen coverage before initiating LHRH agonist therapy in patients with metastatic prostate cancer or high tumor burden risks catastrophic tumor flare with spinal cord compression. 2
  • Discontinuing androgen deprivation therapy after progression to castration-resistant disease; castrate testosterone levels must be maintained lifelong. 2
  • Using antiandrogen monotherapy as primary treatment for metastatic prostate cancer; it is inferior to castration. 2
  • Overlooking cardiovascular risk assessment before initiating therapy; patients with pre-existing cardiac disease require closer monitoring. 1
  • Neglecting to correct electrolyte abnormalities before treatment in patients at risk for QT prolongation. 1
  • Treating uterine fibroids with GnRH agonists for >6 months without bone density monitoring or add-back hormone therapy. 5

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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