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PERJETA

PERTUZUMAB · by ROCHE

ANTINEOPLASTICS Recombinant humanized monoclonal antibody ROCHE

Composition

Inj 420mg/14ml: Pertuzumab 30mg/ml solution for infusion single use vial

Indications & Dosage

Treatment of HER2-positive metastatic or locally recurrent unresectable breast cancer in combination with trastuzumab and docetaxel, in patients who have not received previous anti-HER2 therapy or chemotherapy: BY IV INF: Adults: Initial dose is 840mg IV INF over 60 min, followed by 420 mg IV INF over 30-60 min every 3 weeks.

Administration

Do not administer as an IV push or bolus only IV infusion initial doses over 60 min. Resuscitation facilities should be available.

Precautions

Cardiavascular disease, conditions that could impair left ventricular function, history of congestive heart failure, impaired left ventricular function, prior anthracycline exposure, radiotherapy to the chest area, recent myocardial infarction, serious cardiac arrhythmia, uncontrolled hypertension

Interactions

Anthracyclines, cyclophosphamide.

Pregnancy

Positive evidence of risk: Avoid

Lactation

Contraindicated. Discontinue breast-feeding

Side Effects

Alopecia, anaemia, arthralgia, chills, constipation, cough, decreased appetite, diarrhoea, dizziness, dry skin, dyspepsia, dyspnoea, febrile, neutropenia, headache, increased lacrimation, insomnia, left ventricular dysfunction, leucopenia, malaise, myalgia, nasopharyngitis, oedema, pain, paronychia, peripheral neuropathy, pleural effusion, pruritus, pyrexia, rash, severe hypersensitivity reactions, taste disturbance, nausea, oral mucositis, vomiting, upper respiratory-tract infection. Rare: Interstitial lung disease, bone-marrow suppression, extravasation, hyperuricaemia, thromboembolism, tumour lysis syndrome