Goserelin

Brand names: Zoladex
Drug class: Antineoplastic Agents

Usage of Goserelin

Prostate Cancer

Palliative treatment of advanced prostate cancer. Considered one of several first-line options for hormonal therapy; other options include orchiectomy, estrogens, and antiandrogens.

In clinical studies, goserelin (3.6 mg every 4 weeks) was as effective as orchiectomy. Clinical outcome in patients receiving goserelin 10.8 mg every 12 weeks expected to be similar to that of patients receiving goserelin 3.6 mg every 4 weeks.

Also used as an adjunct to radiation therapy in patients with stage III [C]) prostate cancer.

Treatment of locally confined stage T2b-T4 (B2-C) prostate cancer in conjunction with flutamide and radiation therapy.

Endometriosis

Palliative treatment of endometriosis. Experience with goserelin has been limited to women ≥18 years of age who received consecutive therapy (3.6 mg every 4 weeks) for 6 months.

Breast Cancer

Palliative treatment of advanced breast cancer in premenopausal and perimenopausal women.

Use of ovarian suppression in combination with endocrine therapy (i.e., anastrozole, exemestane, letrozole, tamoxifen)† [off-label] as adjuvant therapy† [off-label] in premenopausal women with early-stage hormone receptor-positive breast cancer† [off-label] may be considered a reasonable choice (accepted).

Dysfunctional Uterine Bleeding

Used as an endometrial-thinning agent prior to endometrial ablation procedures for the treatment of dysfunctional uterine bleeding.

Relate drugs

How to use Goserelin

General

Determine serum testosterone concentrations periodically in patients with prostate cancer in whom the anticipated clinical or biochemical response to goserelin has not been achieved.

Reduction in serum prostate specific antigen (PSA) concentrations may provide information about duration of progression-free status in men with prostate cancer. Do not rely solely on PSA concentrations to monitor response because decreases in PSA concentration may occur independent of tumor response.

Administration

Sub-Q

Administered as a biodegradable implant into the anterior abdominal wall below the navel line.

Implants containing goserelin 3.6 mg are administered every 4 weeks.

Implants containing goserelin 10.8 mg are administered every 12 weeks.

Adherence to the recommended schedule recommended; a delay of a few days is permitted.

The implant may be located by ultrasound in the event that it needs to be removed.

Consult the manufacturer’s labeling for proper methods of administration and associated precautions.

Dosage

Available as goserelin acetate; dosage expressed in terms of goserelin.

Adults

Prostate Cancer Advanced Prostate Cancer Sub-Q

One implant containing 3.6 mg every 4 weeks or one implant containing 10.8 mg every 12 weeks. Intended for long-term administration unless it is clinically inappropriate.

Stage III [C]) prostate cancer (as an adjunct to radiation therapy): One implant containing 3.6 mg every 4 weeks; initiate therapy on the first day of radiation or during the last week of radiation.

Stage B2-C Prostate Cancer Sub-Q

One implant containing 3.6 mg every 4 weeks starting 8 weeks prior to radiation therapy and continuing for a total of 4 doses recommended by the manufacturer. Alternatively, one implant containing 3.6 mg implanted 8 weeks prior to radiation therapy and followed by one implant containing 10.8 mg on day 28 (4 weeks after initial 3.6-mg dose) recommended by the manufacturer.

Endometriosis Sub-Q

One implant containing 3.6 mg every 4 weeks for 6 consecutive months. Retreatment with additional courses currently not recommended; safety has only been established for a 6-month course of therapy; there are concerns about potential long-term effects on bone density. Assess bone density if retreatment for recurrence is considered. (See Musculoskeletal Effects under Cautions.)

Breast Cancer Advanced Breast Cancer Sub-Q

One implant containing 3.6 mg every 4 weeks. Consider dosage increase to 7.2 mg (3.6 mg implanted to 2 different sites) every 4 weeks in women whose serum estradiol concentrations are not reduced to postmenopausal levels after 8 weeks. Intended for long-term administration unless clinically inappropriate.

Early-stage† [off-label] Breast Cancer Sub-Q

Dosage of one implant containing 3.6 mg every 4 weeks has been used in combination with endocrine therapy† [off-label]. (See Breast Cancer under Uses.)

Dysfunctional Uterine Bleeding Sub-Q

One implant containing 3.6 mg 4 weeks before endometrial ablation. Alternatively, the initial 3.6-mg dose of goserelin can be followed by a second 3.6-mg dose 4 weeks after the first dose; surgery should be performed 2–4 weeks after the second dose.

Prescribing Limits

Adults

Endometriosis Sub-Q

Maximum 3.6 mg every 4 weeks for 6 consecutive months.

Special Populations

Hepatic Impairment

Dosage adjustment not needed in patients with mild to moderate hepatic impairment. Not studied in patients with severe hepatic insufficiency.

Renal Impairment

Dosage adjustment not needed. (See Special Populations under Pharmacokinetics.)

Geriatric Patients

Dosage adjustment not needed.

Warnings

Contraindications

  • Known hypersensitivity to goserelin or any ingredient in the formulation, other GnRH agonists, or GnRH.
  • Known or suspected pregnancy unless being used for palliative treatment of advanced breast cancer.
  • Abnormal vaginal bleeding of unknown etiology.
  • The implant containing 10.8 mg of goserelin should not be used in women; insufficient data available to determine whether this preparation is associated with reliable suppression of serum estradiol.

    • Warnings/Precautions

    Sensitivity Reactions

    Hypersensitivity Reactions

    Antibody formation and acute anaphylactic reactions reported with GnRH agonists, including goserelin.

    Fetal/Neonatal Morbidity and Mortality

    Expected hormonal changes increase the risk for pregnancy loss and fetal harm when administered to a pregnant woman; increased risk of pregnancy loss demonstrated in animals.

    Women of childbearing potential should avoid pregnancy and use an effective nonhormonal method of contraception during therapy and for 12 weeks following the last dose of goserelin. Continuous use of goserelin usually inhibits ovulation and stops menstruation; however, prevention of pregnancy is not ensured.

    Exclude pregnancy before initiating therapy in women with benign gynecologic conditions. If a patient with endometriosis or undergoing endometrial thinning becomes pregnant during therapy, discontinue the drug and advise patient about potential fetal hazard.

    If used during pregnancy in women with advanced breast cancer, apprise of potential fetal hazard.

    Endocrine Effects

    Possible worsening of signs and/or symptoms of prostate or breast cancer (e.g., increased bone pain) and/or development of new manifestations due to transient increases in serum testosterone (in men) or estrogen (in women) concentrations during the initial weeks of therapy. Concomitant therapy with an antiandrogen (e.g., bicalutamide, flutamide, nilutamide) 1 week before and during the first few weeks of goserelin therapy may minimize disease flare in men with prostate cancer.

    Spinal cord compression and/or ureteral obstruction reported in men with prostate cancer. If spinal cord compression or renal impairment secondary to ureteral obstruction develops, institute standard treatment of these complications; consider immediate orchiectomy in extreme cases. Caution in patients at particular risk of developing spinal cord compression or ureteral obstruction; observe closely during the first month of therapy. Treat spinal cord compression or ureteral obstruction before initiating goserelin.

    Possible hyperglycemia and increased risk of diabetes in patients receiving GnRH agonists for treatment of prostate cancer. Studies evaluating risk of diabetes in women and children receiving GnRH agonists not performed to date. Evaluate patients for risk factors for diabetes and carefully weigh benefits and risks of GnRH agonist therapy before selecting treatment for prostate cancer. Periodically monitor blood glucose and/or HbA1c in patients receiving GnRH agonists for treatment of prostate cancer. Manage hyperglycemia or diabetes according to current standards of care.

    Possible increase in cervical resistance. Perform cervical dilation carefully following use of goserelin as an endometrial thinning agent.

    Cardiovascular Effects

    Possible increased risk of cardiovascular disease (e.g., MI, sudden cardiac death, stroke) in patients receiving GnRH agonists for treatment of prostate cancer. Studies evaluating risk of cardiovascular disease in women and children receiving GnRH agonists not performed to date.

    Evaluate patients for cardiovascular risk factors and carefully weigh benefits and risks of GnRH agonist therapy before selecting treatment for prostate cancer.

    Periodically monitor patients receiving GnRH agonists for manifestations of cardiovascular disease; manage cardiovascular disease according to current standards of care.

    Cases of serious venous and arterial thromboembolism (e.g., DVT, PE, MI, TIA, stroke) reported in women receiving GnRH agonists.

    Possible transient changes in BP (hypotension or hypertension).

    Possible increased total cholesterol, LDL cholesterol, and triglycerides and decreased HDL cholesterol.

    Musculoskeletal Effects

    Decreases in bone mineral density (BMD), osteoporosis, and bone fracture reported in men; decreases in BMD reported in women. Currently available data suggest that recovery of bone loss occurs following cessation of therapy most women.

    For management of endometriosis in women, concurrent use of hormone replacement therapy or bisphosphonates (e.g., alendronate) may minimize bone mineral loss associated with GnRH agonist therapy without compromising efficacy.

    For treatment of prostate cancer in men, concurrent use of bisphosphonates may minimize bone mineral loss associated with GnRH agonist therapy.

    Risk of BMD loss may be increased in patients with a history of prior therapy that resulted in BMD loss and/or patients with risk factors for decreased BMD (e.g., chronic alcohol abuse, tobacco abuse, family history of osteoporosis, chronic use of anticonvulsants or corticosteroids).

    Hypercalcemia reported in patients with prostate or breast cancer with bone metastases. Initiate appropriate treatment if hypercalcemia develops.

    Prolongation of QT Interval

    Possible QT-interval prolonlgation. Consider monitoring ECG and serum electrolyte concentrations periodically during therapy. Correct electrolyte abnormalities.

    Weigh benefits and risks of androgen deprivation therapy in patients with congenital long QT syndrome, electrolyte abnormalities, or CHF and in patients taking drugs known to prolong the QT interval.

    Local Reactions

    Injection site injury and vascular injury (e.g., pain, hematoma, hemorrhage, hemorrhagic shock) requiring blood transfusion and surgical intervention reported.

    Administer with caution in patients with low BMI and/or those receiving full-dose anticoagulation therapy.

    Pituitary Apoplexy

    Pituitary apoplexy, a clinical syndrome resulting from infarction of the pituitary gland, and pituitary adenoma reported rarely. Most cases occur within 2 weeks of the first dose, sometimes within the first hour. If manifestations occur (e.g., sudden headache, vomiting, visual changes, ophthalmoplegia, altered mental status, sometimes cardiovascular collapse), immediate medical attention required.

    Specific Populations

    Pregnancy

    May cause fetal harm. (See Fetal/Neonatal Morbidity and Mortality under Cautions.)

    Lactation

    Distributed into milk in rats; not known whether distributed into human milk. Discontinue nursing or the drug.

    Pediatric Use

    Safety and efficacy not established.

    Geriatric Use

    Clinical studies for use in prostate cancer have been conducted principally in patients ≥65 years of age. Clinical studies in women >65 years of age not performed to date.

    Renal Impairment

    Incidence of adverse effects not increased in patients with renal impairment receiving goserelin 10.8 mg.

    Common Adverse Effects

    Men: Hot flushes (flashes), sexual dysfunction, decreased erections, lower urinary tract symptoms, pain (worsened in the first month).

    Women: Hot flushes (flashes), vaginitis, headache, emotional lability, decreased/increased libido, sweating, depression, acne, breast atrophy, breast enlargement.

    What other drugs will affect Goserelin

    No formal drug interaction studies to date.

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