Systemic Anti-Cancer Therapy Regimen Library
GU Renal cell Metastatic - beVACizumab and erlotinib
Treatment Overview
This regimen contains a medicine where one or more biosimilars may exist. Any biosimilars used have been reviewed by the regulator (Medsafe) and relevant specialists were consulted nationally. Where regulators, in consultation with relevant specialists, have agreed that there are no clinically significant differences in either safety or effectiveness between a biosimilar and originator product, these drugs may be used interchangeably.
Cycle 1 (and all further cycles) - 28 days
Cycle details
Cycle 1 (and all further cycles) - 28 days
Medication | Dose | Route | Days | Max Duration |
---|---|---|---|---|
doxycycline * | 100 mg Once daily | oral administration | 0 | |
hydrocortisone * | 1 % Once daily | topical administration | 0 | |
cetostearyl alcohol + paraffin liquid + paraffin soft white | 50 g Once daily | topical administration | 0 | |
avobenzone + homosalate + octisalate + octocrilene + oxybenzone | 50 g | topical administration | 0 | |
beVACizumab * | 10 mg/kg | intravenous | 1, 15 | 90 minutes |
erlotinib * | 150 mg Once daily | oral administration | 1 to 28 | |
loperamide | 2 mg | oral administration | 1 |
Full details
Cycle 1 (and all further cycles) - 28 days
Day: 0
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
doxycycline * | 100 mg Once daily | oral administration |
Instructions:
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hydrocortisone * | 1 % Once daily | topical administration |
Instructions:
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cetostearyl alcohol + paraffin liquid + paraffin soft white | 50 g Once daily | topical administration |
Instructions:
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avobenzone + homosalate + octisalate + octocrilene + oxybenzone | 50 g | topical administration |
Instructions:
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Day: 1
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
beVACizumab * | 10 mg/kg | intravenous | 90 minutes |
Instructions:
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erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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loperamide | 2 mg | oral administration |
Instructions:
Take TWO capsules (=4 mg) at onset of loose bowel motions and a further ONE capsule (=2 mg) for every loose bowel motion (maximum of EIGHT capsules in 24 hours), or use as directed by oncologist or haematologist. |
Day: 2
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 3
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 4
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 5
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 6
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 7
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 8
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 9
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 10
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 11
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 12
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 13
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 14
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 15
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
beVACizumab * | 10 mg/kg | intravenous | 90 minutes |
Instructions:
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erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 16
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 17
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 18
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 19
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 20
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 21
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 22
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 23
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 24
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 25
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 26
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 27
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Day: 28
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
erlotinib * | 150 mg Once daily | oral administration |
Instructions:
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Supportive Care Factors
Factor | Value |
---|---|
Diarrhoea risk: | Anti-diarrhoeals are usually prescribed with this treatment |
Emetogenicity: | Minimal to low |
Hypersensitivity / Infusion related reaction risk: | Low - routine premedication not recommended |
Emetogenicity: Antiemetics may be required with continuous dosing of oral anti-cancer medicines with MINIMAL to LOW emetic risk; an individualised approach is appropriate.
References
Srinivasan R, Gurram S, Al Harthy M, et al. Results from a phase II study of bevacizumab and erlotinib in subjects with advanced hereditary leiomyomatosis and renal cell cancer (HLRCC) or sporadic papillary renal cell cancer. Journal of Clinical Oncology 2020;38:5004-5004. https://doi.org/10.1200/JCO.2020.38.15_suppl.5004.
Srinivasan R, Su D, Stamatakis L, et al. Mechanism based targeted therapy for hereditary leiomyomatosis and renal cell cancer (HLRCC) and sporadic papillary renal cell carcinoma: interim results from a phase 2 study of bevacizumab and erlotinib [abstract]. Eur J Cancer 2014;50:8. http://www.ejcancer.com/article/S0959-8049(14)70131-5/abstract.
Roche Products (New Zealand) Limited. Tarceva New Zealand Data Sheet 19 July 2022 https://www.medsafe.govt.nz/profs/Datasheet/t/tarcevatab.pdf (Accessed 30 September 2022).
Roche Products (New Zealand) Limited. Avastin New Zealand Data Sheet. 21 December 2021 https://www.medsafe.govt.nz/profs/datasheet/a/Avastininf.pdf (Accessed 30 September 2022).
* 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.