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Systemic Anti-Cancer Therapy Regimen Library

UGI OES NON-Metastatic - mitomycin and fluorouracil chemoradiation [MSKCC]

Treatment Overview

Commence regimen in relation to radiation therapy as per institutional policy.

Cycle 1 - 56 days

Cycle length:
56

Cycle details

Cycle 1 - 56 days

Medication Dose Route Days Max Duration
ondansetron 8 mg oral administration 1, 29
mitomycin * 8 mg/m² Cap dose per administration at: 18 mg intravenous 1 15 minutes
fluorouracil * 3000 mg/m² intravenous 1, 29 96 hours Min: 96 hours
domperidone 10 mg Three times daily oral administration 1
loperamide 2 mg oral administration 1

Full details

Cycle 1 - 56 days

Day: 1

Medication Dose Route Max duration Details
ondansetron 8 mg oral administration
Instructions:
ONE hour prior to chemotherapy. Alternative is dexamethasone 4 mg.
mitomycin * 8 mg/m² Cap dose per administration at: 18 mg 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.
fluorouracil * 3000 mg/m² intravenous 96 hours Min: 96 hours
Instructions:
Continuous infusion via pump over 96 hours.
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: 29

Medication Dose Route Max duration Details
ondansetron 8 mg oral administration
Instructions:
ONE hour prior to chemotherapy. Alternative is dexamethasone 4 mg.
fluorouracil * 3000 mg/m² intravenous 96 hours Min: 96 hours
Instructions:
Continuous infusion via pump over 96 hours.

Supportive Care Factors

Factor Value
Diarrhoea risk: Anti-diarrhoeals are usually prescribed with this treatment
Emetogenicity: Low
Hypersensitivity / Infusion related reaction risk: Low - routine premedication not recommended

* 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.