Systemic Anti-Cancer Therapy Regimen Library
amivantamab 1050 mg (LUNG NSCLC Locally advanced/Metastatic - amivantamab )
Treatment Overview
Recommended starting dose for body-weight less than 80 kg.
Cycle 1 - 28 days
dexamethasone:
- Days 1 and 2: dexamethasone premedication is required;
- Days 8, 15 and 22: dexamethasone premedication may be omitted if no infusion-related reaction occurred during previous infusions. If dexamethasone is omitted, the clinician may consider ondansetron 8 mg ONE hour prior to amivantamab infusion for antiemetic cover.
Cycle 2 (and all further cycles) - 28 days
amivantamab:
- Administer dexamethasone 10 mg IV 45 to 60 minutes prior to amivantamab if an infusion-related reaction occurred during previous infusions.
- If dexamethasone is administered, ondansetron 8 mg ONE hour prior to amivantamab infusion for antiemetic cover may be omitted.
Cycle details
Cycle 1 - 28 days
Medication | Dose | Route | Days | Max Duration |
---|---|---|---|---|
dexamethasone * | 10 mg flat dosing | intravenous | 1, 2, 8, 15, 22 |
15 minutes |
loratadine * | 10 mg | oral administration | 1, 2, 8, 15, 22 |
|
paracetamol | 1000 mg flat dosing | oral administration | 1, 2, 8, 15, 22 |
|
amivantamab | 350 mg flat dosing | intravenous | 1 | 5 hours |
amivantamab | 700 mg flat dosing | intravenous | 2 | 5 hours |
amivantamab | 1050 mg flat dosing | intravenous | 8, 15, 22 | 3 hours |
domperidone | 10 mg Three times daily | oral administration | 1 |
dexamethasone:
- Days 1 and 2: dexamethasone premedication is required;
- Days 8, 15 and 22: dexamethasone premedication may be omitted if no infusion-related reaction occurred during previous infusions. If dexamethasone is omitted, the clinician may consider ondansetron 8 mg ONE hour prior to amivantamab infusion for antiemetic cover.
Cycle 2 (and all further cycles) - 28 days
Medication | Dose | Route | Days | Max Duration |
---|---|---|---|---|
ondansetron | 8 mg | oral administration | 1, 15 | |
loratadine * | 10 mg | oral administration | 1, 15 | |
paracetamol | 1000 mg flat dosing | oral administration | 1, 15 | |
amivantamab | 1050 mg flat dosing | intravenous | 1, 15 | 2 hours |
domperidone | 10 mg Three times daily | oral administration | 1 |
amivantamab:
- Administer dexamethasone 10 mg IV 45 to 60 minutes prior to amivantamab if an infusion-related reaction occurred during previous infusions.
- If dexamethasone is administered, ondansetron 8 mg ONE hour prior to amivantamab infusion for antiemetic cover may be omitted.
Full details
Cycle 1 - 28 days
Day: 1
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
dexamethasone * | 10 mg flat dosing | intravenous | 15 minutes |
Instructions:
45 to 60 minutes prior to amivantamab, or as per institutional practice. |
loratadine * | 10 mg | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
paracetamol | 1000 mg flat dosing | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
amivantamab | 350 mg flat dosing | intravenous | 5 hours |
Instructions:
Additional details:
|
domperidone | 10 mg Three times daily | oral administration |
Instructions:
When required for nausea and/or vomiting.
|
Day: 2
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
dexamethasone * | 10 mg flat dosing | intravenous | 15 minutes |
Instructions:
45 to 60 minutes prior to amivantamab, or as per institutional practice. |
loratadine * | 10 mg | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
paracetamol | 1000 mg flat dosing | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
amivantamab | 700 mg flat dosing | intravenous | 5 hours |
Instructions:
Additional details:
|
Day: 8
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
dexamethasone * | 10 mg flat dosing | intravenous | 15 minutes |
Instructions:
45 to 60 minutes prior to amivantamab, or as per institutional practice.
|
loratadine * | 10 mg | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
paracetamol | 1000 mg flat dosing | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
amivantamab | 1050 mg flat dosing | intravenous | 3 hours |
Instructions:
Additional details:
|
Day: 15
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
dexamethasone * | 10 mg flat dosing | intravenous | 15 minutes |
Instructions:
45 to 60 minutes prior to amivantamab, or as per institutional practice.
|
loratadine * | 10 mg | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
paracetamol | 1000 mg flat dosing | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
amivantamab | 1050 mg flat dosing | intravenous | 3 hours |
Instructions:
Additional details:
|
Day: 22
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
dexamethasone * | 10 mg flat dosing | intravenous | 15 minutes |
Instructions:
45 to 60 minutes prior to amivantamab, or as per institutional practice.
|
loratadine * | 10 mg | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
paracetamol | 1000 mg flat dosing | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
amivantamab | 1050 mg flat dosing | intravenous | 3 hours |
Instructions:
Additional details:
|
Cycle 2 (and all further cycles) - 28 days
Day: 1
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
ondansetron | 8 mg | oral administration |
Instructions:
ONE hour prior to amivantamab infusion.
|
|
loratadine * | 10 mg | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
paracetamol | 1000 mg flat dosing | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
amivantamab | 1050 mg flat dosing | intravenous | 2 hours |
Instructions:
Additional details:
|
domperidone | 10 mg Three times daily | oral administration |
Instructions:
When required for nausea and/or vomiting.
|
Day: 15
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
ondansetron | 8 mg | oral administration |
Instructions:
ONE hour prior to amivantamab infusion.
|
|
loratadine * | 10 mg | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
paracetamol | 1000 mg flat dosing | oral administration |
Instructions:
30 to 60 minutes prior to amivantamab. |
|
amivantamab | 1050 mg flat dosing | intravenous | 2 hours |
Instructions:
Additional details:
|
Additional details
Section 1: Infusion rates
Table from: Rybrevant New Zealand Datasheet (Accessed 06 August 2024).
Supportive Care Factors
Factor | Value |
---|---|
Emetogenicity: | Low |
Hypersensitivity / Infusion related reaction risk: | High - routine premedication recommended |
References
Janssen-Cilag (New Zealand) Limited. Rybrevant New Zealand Datasheet 19 February 2024. https://www.medsafe.govt.nz/profs/datasheet/r/rybrevantinf.pdf (Accessed 06 August 2024)
* The medicines, doses, combinations, and schedule in this treatment regimen have been carefully reviewed against international best practice guidelines by specialists in medical oncology around New Zealand and this advice has been accepted for publication by Te Aho o Te Kahu (the Cancer Control Agency). Sometimes medicines that are used in routine clinical practice have not been through a formal review process by the NZ Medicines Regulator Medsafe and are therefore considered unapproved or off-label. These medicines are legally able to be prescribed through sections 25 and 29 of the Medicines Act and by obtaining informed consent from patients. All treatment regimens listed on this website have been through robust peer review and are considered an accepted standard of care, whether prescribed through sections 25 or 29 or carrying formal Medsafe Approval.
s29: This symbol indicates that some formulations of the associated medicine are legally only able to be prescribed under section 29 of the Medicines Act. You can see which formulations are section 29 by hovering over the s29 symbol. You can access full medication details from the New Zealand Formulary by clicking on the medication name. Each clinician retains full responsibility for ensuring they have complied with all relevant obligations and requirements of section 29 including obtaining informed patient consent prior to prescribing the applicable medicine.