
Perjeta420 mg/14
Roche Bangladesh Ltd.
Pertuzumab is a HER2-targeted monoclonal antibody approved only for use in combination regimens for HER2-positive breast cancer and more.
Pertuzumab is a HER2-targeted monoclonal antibody approved only for use in combination regimens for HER2-positive breast cancer, based on confirmed HER2 overexpression/gene amplification by an FDA-approved test. It is not used as monotherapy.
| Setting | Combination | Patient population |
|---|---|---|
| Neoadjuvant (before surgery) | With trastuzumab and chemotherapy | HER2-positive, locally advanced, inflammatory, or early-stage breast cancer (tumor greater than 2 cm or node-positive), as part of a complete treatment regimen |
| Adjuvant (after surgery) | With trastuzumab and chemotherapy | HER2-positive early breast cancer at high risk of recurrence |
| Metastatic | With trastuzumab and docetaxel | HER2-positive metastatic breast cancer in patients who have not received prior anti-HER2 therapy or chemotherapy for metastatic disease |
Pertuzumab is not approved for HER2-negative breast cancer or for cancers other than breast cancer, and is not established as effective outside of these specific combination regimens.
Pertuzumab should be used only after confirming HER2 positivity by a validated test, and is always given in combination with trastuzumab and chemotherapy, administered by intravenous infusion under the supervision of a physician experienced in cancer chemotherapy.
| Dose | Regimen |
|---|---|
| Initial (loading) dose | 840 mg by IV infusion over 60 minutes |
| Maintenance dose | 420 mg by IV infusion over 30 to 60 minutes, every 3 weeks, together with trastuzumab and chemotherapy, for the number of cycles specified by the approved regimen being used |
Pertuzumab and trastuzumab are withheld for a significant drop in left ventricular ejection fraction (LVEF) and resumed only if LVEF recovers per protocol criteria. No dose reduction of Pertuzumab is recommended for any indication; a dose is either given in full or withheld.
The most common side effects, occurring in more than 30% of patients receiving Pertuzumab-based combination regimens, include:
Pertuzumab is contraindicated in patients with known hypersensitivity to Pertuzumab or to any of its excipients.
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