Trastuzumab
(tra-stu′zu-mab)
Herceptin
Classifications: IMMUNOMODULATOR; MONOCLONAL ANTIBODY; ANTINEOPLASTIC; ANTI-HUMAN EPIDERMAL GROWTH FACTOR (ANTI-HER)
Therapeutic:
ANTINEOPLASTIC; IMMUNOMODULATOR; ANTI-HER
Pregnancy Category: D
AVAILABILITY
Solution for injection
ACTION & THERAPEUTIC EFFECT
Recombinant DNA monoclonal
antibody (IgG1 kappa) that selectively binds to the human
epidermal growth factor receptor-2 protein (HER2). Inhibits growth of human tumor cells that overexpress HER2 proteins.
USES
Metastatic breast cancer in those
whose tumors overexpress the HER2 protein. HER2-positive breast cancer after surgery.
CONTRAINDICATIONS
Concurrent administration of
anthracycline or radiation; pregnancy (category D); lactation during and for 6
mo following administration of trastuzumab.
CAUTIOUS USE
Preexisting cardiac dysfunction;
pulmonary disease; previous administration of cardiotoxic therapy (e.g.,
anthracycline or radiation); hypersensitivity to benzyl alcohol; older adults.
ROUTE & DOSAGE
Metastatic Breast Cancer
|
Trastuzumab (Herceptin) Uses, Dosage, Side Effects |
Adult:
IV 4 mg/kg, then 2 mg/kg qwk
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ADMINISTRATION
Intravenous
PREPARE:
IV Infusion: Reconstitute each vial with 20
mL of supplied diluent (bacteriostatic water) to produce a multidose vial
containing 21 mg/mL.
- Note: For patients with a hypersensitivity to
benzyl alcohol, reconstitute with sterile water for injection; this solution must be used immediately with any unused
portion discarded.
- Withdraw the ordered dose and add to a 250 mL of
NS and invert bag to mix.
- Do not give or mix with dextrose solutions.
ADMINISTER:
IV Infusion: Infuse loading dose (4 mg/kg)
over 90 min; infuse subsequent doses (2 mg/kg) over 30 min.
- Do not give
IV push or as a bolus dose.
INCOMPATIBILITIES:
Solution/additive: Dextrose solution; do not mix or coadminister with other
drugs.
- Store unopened vials and
reconstituted vials at 2°–8° C (36°–46° F).
- Discard reconstituted vials 28 days
after reconstitution.
ADVERSE EFFECTS (≥1%)
Body as a Whole: Pain, asthenia, fever,
chills, flu syndrome, allergic reaction,
bone pain, arthralgia,
hypersensitivity (anaphylaxis, urticaria, bronchospasm, angioedema, or hypotension), increased incidence of infections,
infusion reaction (chills, fever, nausea, vomiting, pain, rigors,
headache, dizziness, dyspnea, hypotension, rash). CNS: Headache, insomnia, dizziness, paresthesias, depression, peripheral neuritis, neuropathy. CV: CHF, cardiac dysfunction (dyspnea, cough, paroxysmal
nocturnal dyspnea, peripheral edema, S3 gallop, reduced ejection fraction), tachycardia, edema,
cardiotoxicity. GI: Diarrhea,
abdominal pain, nausea,
vomiting, anorexia. Hematologic: Anemia, leukopenia. Respiratory: Cough, dyspnea, rhinitis, pharyngitis, sinusitis. Skin: Rash, herpes simplex, acne.
INTERACTIONS
Drug: Paclitaxel may increase trastuzumab levels and toxicity.
PHARMACOKINETICS
Half-Life: 5.8 days.
NURSING IMPLICATIONS
Black Box
Warning
Trastuzumab
has been associated with cardiomyopathy, infusion reactions, pulmonary
toxicity, and embryo-fetal toxicity.
Assessment & Drug Effects
- Monitor for
infusion reactions within 24 h of infusion. Stop infusion and notify prescriber
if patients develop dyspnea, significant hypotension, or any other sign of
infusion reaction. Monitor closely until symptoms resolve. chills and fever
during the first IV infusion; these adverse events usually respond to prompt
treatment without the need to discontinue the infusion. Notify prescriber immediately.
- Monitor carefully cardiovascular status at baseline and
throughout course of therapy, assessing for S&S of heart failure (e.g.,
dyspnea, increased cough, PND, edema, S3 gallop). Those with preexisting
cardiac dysfunction are at high risk for cardiotoxicity.
- Monitor lab tests: Periodic CBC with differential, platelet
count, and Hgb and Hct.
Patient & Family Education
- Report promptly any unusual symptoms (e.g., chills, nausea,
fever) during infusion.
- Report promptly any of the following: Shortness of breath, swelling
of feet or legs, persistent cough, difficulty sleeping, loss of appetite,
abdominal bloating.
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