Menu Close Menu

Fewer cancers.
Better survival.
Equity for all.

Systemic Anti-Cancer Therapy Regimen Library

LYM Relapsed - GIVE [filgrastim, IFOSFamide, etoposide and epirubicin]

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.

Cycles 1 to 3 - 21 days

Cycle length:
21

If for stem cell harvest, mobilise after cycle 2 or as per institutional practice.


Mesna dosing, as per Bishton 2007 (see Reference below).

Cycle details

Cycles 1 to 3 - 21 days

Medication Dose Route Days Max Duration
epirubicin 50 mg/m² intravenous 1 15 minutes
etoposide (as phosphate) * 200 mg/m² Once daily intravenous 1, 2, 3 60 minutes
sodium chloride 0.9 % intravenous 1 120 minutes
mesna * 1800 mg/m² intravenous 1 15 minutes
IFOSFamide * 3000 mg/m² Once daily intravenous 1, 2, 3 24 hours Min: 24 hours
mesna 3000 mg/m² Once daily intravenous 1, 2, 3 24 hours Min: 24 hours
mesna * 5400 mg/m² intravenous 4 12 hours Min: 12 hours
filgrastim 5 microgram/kg Once daily subcutaneous injection 5 to 10

If for stem cell harvest, mobilise after cycle 2 or as per institutional practice.


Mesna dosing, as per Bishton 2007 (see Reference below).

Full details

Cycles 1 to 3 - 21 days

Day: 1

Medication Dose Route Max duration Details
epirubicin 50 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.

etoposide (as phosphate) * 200 mg/m² Once daily intravenous 60 minutes
sodium chloride 0.9 % intravenous 120 minutes
Quantity:1000 mL
Instructions:

Prior to IFOSFamide infusion.

mesna * 1800 mg/m² intravenous 15 minutes
Instructions:

Immediately prior to the first dose of IFOSFamide.

IFOSFamide * 3000 mg/m² Once daily intravenous 24 hours Min: 24 hours
Instructions:

Admixed with mesna 3000 mg/m2 and administer by continuous infusion over 24 hours.

Recommended daily hydration is 3000 ml per day as oral or IV fluid on day(s) of IFOSFamide and for 24 hours after, or as per institutional practice.

mesna 3000 mg/m² Once daily intravenous 24 hours Min: 24 hours
Instructions:

Admixed with IFOSFamide and administer by continuous infusion over 24 hours.

Day: 2

Medication Dose Route Max duration Details
etoposide (as phosphate) * 200 mg/m² Once daily intravenous 60 minutes
IFOSFamide * 3000 mg/m² Once daily intravenous 24 hours Min: 24 hours
Instructions:

Admixed with mesna 3000 mg/m2 and administer by continuous infusion over 24 hours.

Recommended daily hydration is 3000 ml per day as oral or IV fluid on day(s) of IFOSFamide and for 24 hours after, or as per institutional practice.

mesna 3000 mg/m² Once daily intravenous 24 hours Min: 24 hours
Instructions:

Admixed with IFOSFamide and administer by continuous infusion over 24 hours.

Day: 3

Medication Dose Route Max duration Details
etoposide (as phosphate) * 200 mg/m² Once daily intravenous 60 minutes
IFOSFamide * 3000 mg/m² Once daily intravenous 24 hours Min: 24 hours
Instructions:

Admixed with mesna 3000 mg/m2 and administer by continuous infusion over 24 hours.

Recommended daily hydration is 3000 ml per day as oral or IV fluid on day(s) of IFOSFamide and for 24 hours after, or as per institutional practice.

mesna 3000 mg/m² Once daily intravenous 24 hours Min: 24 hours
Instructions:

Admixed with IFOSFamide and administer by continuous infusion over 24 hours.

Day: 4

Medication Dose Route Max duration Details
mesna * 5400 mg/m² intravenous 12 hours Min: 12 hours
Instructions:

Start immediately after last IFOSFamide infusion.

Day: 5

Medication Dose Route Max duration Details
filgrastim 5 microgram/kg Once daily subcutaneous injection
Instructions:
Round dose to nearest prefilled syringe dose of 300 micrograms or 480 micrograms.

Day: 6

Medication Dose Route Max duration Details
filgrastim 5 microgram/kg Once daily subcutaneous injection
Instructions:
Round dose to nearest prefilled syringe dose of 300 micrograms or 480 micrograms.

Day: 7

Medication Dose Route Max duration Details
filgrastim 5 microgram/kg Once daily subcutaneous injection
Instructions:
Round dose to nearest prefilled syringe dose of 300 micrograms or 480 micrograms.

Day: 8

Medication Dose Route Max duration Details
filgrastim 5 microgram/kg Once daily subcutaneous injection
Instructions:
Round dose to nearest prefilled syringe dose of 300 micrograms or 480 micrograms.

Day: 9

Medication Dose Route Max duration Details
filgrastim 5 microgram/kg Once daily subcutaneous injection
Instructions:
Round dose to nearest prefilled syringe dose of 300 micrograms or 480 micrograms.

Day: 10

Medication Dose Route Max duration Details
filgrastim 5 microgram/kg Once daily subcutaneous injection
Instructions:
Round dose to nearest prefilled syringe dose of 300 micrograms or 480 micrograms.

Supportive Care Factors

Factor Value
Antiviral prophylaxis for herpes virus: Routine antiviral prophylaxis may be considered
Emetogenicity: High
Growth factor support: Recommended for primary prophylaxis
Hydration: Routine hydration recommended
Irradiated blood components: Variable
Mesna uroprotection: Routine mesna uroprotection recommended
Tumour lysis syndrome prophylaxis: Tumour lysis syndrome prophylaxis may be considered

Antiviral prophylaxis for hepatitis B virus: Guidance is limited to high-risk anti-cancer medicines. Clinicians will need to assess individual patient risk for other anti-cancer medicines.

Irradiated blood components: Required for Hodgkin lymphoma patients at all stages of disease and therapy. Continue indefinitely.

References

Bishton, M. J., R. J. Lush, J. L. Byrne, et al. 2007. "Ifosphamide, etoposide and epirubicin is an effective combined salvage and peripheral blood stem cell mobilisation regimen for transplant-eligible patients with non-Hodgkin lymphoma and Hodgkin disease." Br J Haematol 136(5):752-761., PMID: 17313378

McQuaker, I. G., A. P. Haynes, C. Stainer, et al. 1997. "Stem cell mobilization in resistant or relapsed lymphoma: superior yield of progenitor cells following a salvage regimen comprising ifosphamide, etoposide and epirubicin compared to intermediate-dose cyclophosphamide." Br J Haematol 98(1):228-233. , PMID: 9233591

Zinzani, P. L., E. Barbieri, G. Visani, et al. 1994. "Ifosfamide, epirubicin and etoposide (IEV) therapy in relapsed and refractory high-grade non-Hodgkin's lymphoma and Hodgkin's disease." Haematologica 79(6):508-512., PMID: 7534744

Bishton, M. J. and A. P. Haynes. 2007. "Combination chemotherapy followed by autologous stem cell transplant for enteropathy-associated T cell lymphoma." Br J Haematol 136(1):111-113. , PMID: 17116129

Zinzani, P. L., M. Tani, A. L. Molinari, et al. 2002. "Ifosfamide, epirubicin and etoposide regimen as salvage and mobilizing therapy for relapsed/refractory lymphoma patients." Haematologica 87(8):816-821. , PMID: 12161357

Tabernero J, Vyas M, Giuliani R, Arnold D, Cardoso F, Casali PG, Cervantes A, Eggermont AMM, Eniu A, Jassem J, Pentheroudakis G, Peters S, Rauh S, Zielinski CC, Stahel RA, Voest E, Douillard JY, McGregor K, Ciardiello F. Biosimilars: a position paper of the European Society for Medical Oncology, with particular reference to oncology prescribers. ESMO Open. 2017 Jan 16;1(6):e000142. doi: 10.1136/esmoopen-2016-000142., PMID: 28848668

Lyman GH, Balaban E, Diaz M, Ferris A, Tsao A, Voest E, Zon R, Francisco M, Green S, Sherwood S, Harvey RD, Schilsky RL. American Society of Clinical Oncology Statement: Biosimilars in Oncology. J Clin Oncol. 2018 Apr 20;36(12):1260-1265. doi: 10.1200/JCO.2017.77.4893. Epub 2018 Feb 14., PMID: 29443651

New Zealand Blood Service Transfusion Medicine Handbook Third Edition, 2016 https://www.nzblood.co.nz/assets/Transfusion-Medicine/PDFs/111G122.pdf (accessed 16 June 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.