Systemic Anti-Cancer Therapy Regimen Library
BR Adjuvant - EC-D [epirubicin and CYCLOPHOSPHamide followed by DOCEtaxel]
Treatment Overview
This regimen consists of two parts: EC [epirubicin and CYCLOPHOSPHamide] followed by DOCEtaxel.
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.
Cycles 1 to 4 - 21 days - EC [epirubicin and CYCLOPHOSPHamide]
Cycle specific Supportive Care Factors:
Emetogenicity: HIGH.
Cycles 5 to 8 - 21 days - DOCEtaxel
Some centres may wish to replace the three oral doses of dexamethasone 8 mg premedication with a single intravenous dose of dexamethasone 20 mg prior to DOCEtaxel infusion.
Cycle specific Supportive Care Factors:
Diarrhoea risk: Anti-diarrhoeals are usually prescribed with this treatment.
Emetogenicity: LOW.
Growth factor support: Recommended for primary prophylaxis.
Hypersensitivity / Infusion related reaction risk: HIGH - routine premedication recommended.
Cycle details
Cycles 1 to 4 - 21 days - EC [epirubicin and CYCLOPHOSPHamide]
Medication | Dose | Route | Days | Max Duration |
---|---|---|---|---|
olanzapine * | 5 mg | oral administration | 1 to 4 | |
aprepitant | 125 mg | oral administration | 1 | |
aprepitant | 80 mg | oral administration | 2, 3 | |
dexamethasone * | 12 mg | oral administration | 1 | |
dexamethasone * | 8 mg | oral administration | 2, 3, 4 | |
ondansetron | 8 mg | oral administration | 1 | |
epirubicin | 90 mg/m² | intravenous | 1 | 15 minutes |
CYCLOPHOSPHamide | 600 mg/m² | intravenous | 1 | 60 minutes |
ondansetron | 8 mg | oral administration | 1 | |
cycliZINE | 50 mg Three times daily | oral administration | 1 |
Cycle specific Supportive Care Factors:
Emetogenicity: HIGH.
Cycles 5 to 8 - 21 days - DOCEtaxel
Medication | Dose | Route | Days | Max Duration |
---|---|---|---|---|
dexamethasone * | 8 mg Twice daily | oral administration | 0, 1, 2 | |
DOCEtaxel | 100 mg/m² | intravenous | 1 | 60 minutes |
pegFILGRASTIM | 6 mg | subcutaneous injection | 2 | |
domperidone | 10 mg Three times daily | oral administration | 1 | |
loperamide | 2 mg | oral administration | 1 |
Some centres may wish to replace the three oral doses of dexamethasone 8 mg premedication with a single intravenous dose of dexamethasone 20 mg prior to DOCEtaxel infusion.
Cycle specific Supportive Care Factors:
Diarrhoea risk: Anti-diarrhoeals are usually prescribed with this treatment.
Emetogenicity: LOW.
Growth factor support: Recommended for primary prophylaxis.
Hypersensitivity / Infusion related reaction risk: HIGH - routine premedication recommended.
Full details
Cycles 1 to 4 - 21 days - EC [epirubicin and CYCLOPHOSPHamide]
Day: 1
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
olanzapine * | 5 mg | oral administration |
Instructions:
ONE hour prior to chemotherapy.
|
|
aprepitant | 125 mg | oral administration |
Instructions:
ONE hour prior to chemotherapy. |
|
dexamethasone * | 12 mg | oral administration |
Instructions:
ONE hour prior to chemotherapy with food. |
|
ondansetron | 8 mg | oral administration |
Instructions:
ONE hour prior to chemotherapy. |
|
epirubicin | 90 mg/m² | intravenous | 15 minutes |
Instructions:
Warning vesicant—ensure vein is patent prior to administration, administer vesicant as per institutional policy and monitor for signs of extravasation throughout administration. |
CYCLOPHOSPHamide | 600 mg/m² | intravenous | 60 minutes | |
ondansetron | 8 mg | oral administration |
Instructions:
EIGHT hours after chemotherapy OR before bed. |
|
cycliZINE | 50 mg Three times daily | oral administration |
Instructions:
When required for nausea and/or vomiting.
|
Day: 2
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
olanzapine * | 5 mg | oral administration |
Instructions:
ONCE daily. This medicine may make you sleepy and make it dangerous to drive or operate machinery. Limit alcohol intake. |
|
aprepitant | 80 mg | oral administration |
Instructions:
ONCE daily in the morning. |
|
dexamethasone * | 8 mg | oral administration |
Instructions:
ONCE daily in the morning with food. Dose and duration may be individualised at clinician’s discretion. |
Day: 3
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
olanzapine * | 5 mg | oral administration |
Instructions:
ONCE daily. This medicine may make you sleepy and make it dangerous to drive or operate machinery. Limit alcohol intake. |
|
aprepitant | 80 mg | oral administration |
Instructions:
ONCE daily in the morning. |
|
dexamethasone * | 8 mg | oral administration |
Instructions:
ONCE daily in the morning with food. Dose and duration may be individualised at clinician’s discretion. |
Day: 4
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
olanzapine * | 5 mg | oral administration |
Instructions:
ONCE daily. This medicine may make you sleepy and make it dangerous to drive or operate machinery. Limit alcohol intake. |
|
dexamethasone * | 8 mg | oral administration |
Instructions:
ONCE daily in the morning with food. Dose and duration may be individualised at clinician’s discretion. |
Cycles 5 to 8 - 21 days - DOCEtaxel
Day: 0
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
dexamethasone * | 8 mg Twice daily | oral administration |
Instructions:
Take with food. |
Day: 1
Medication | Dose | Route | Max duration | Details |
---|---|---|---|---|
dexamethasone * | 8 mg Twice daily | oral administration |
Instructions:
Take with food. |
|
DOCEtaxel | 100 mg/m² | intravenous | 60 minutes |
Instructions:
Prepare solution in PVC-free bag and administer via polyethylene lined administration set. Please carry out graded challenge as per institutional policy. |
domperidone | 10 mg Three times daily | oral administration |
Instructions:
When required for nausea and/or vomiting. The choice of rescue antiemetic may be substituted to reflect institutional policy or individual patient characteristics. |
|
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 |
---|---|---|---|---|
dexamethasone * | 8 mg Twice daily | oral administration |
Instructions:
Take with food. |
|
pegFILGRASTIM | 6 mg | subcutaneous injection |
Supportive Care Factors
Factor | Value |
---|---|
Diarrhoea risk: | Variable |
Emetogenicity: | Variable |
Growth factor support: | Variable |
Hypersensitivity / Infusion related reaction risk: | Variable |
References
Rogers, E. S., E. Witton, J. Stewart, and D. Porter. "Efficacy and safety of a single dose of dexamethasone pre docetaxel treatment: The Auckland experience." Annals of Oncology 25 (2014): iv537.
* 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.