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Systemic Anti-Cancer Therapy Regimen Library

LYM NHL T-cell - CHOEP14 [CYCLOPHOSPHamide, DOXOrubicin, etoposide, vinCRISTine and prEDNISone] [IV/oral etoposide]

Treatment Overview

Use CHOEP14 with caution in patients over 60 years of age.


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 6 - 14 days

Cycle length:
14

If for stem cell harvest, mobilise as per institutional practice.

Cycle details

Cycles 1 to 6 - 14 days

Medication Dose Route Days Max Duration
prEDNISone 100 mg flat dosing Once daily oral administration 1 to 5
DOXOrubicin * 50 mg/m² intravenous 1 15 minutes
vinCRISTine 1.4 mg/m² Cap dose per administration at: 2 mg intravenous 1 10 minutes
etoposide (as phosphate) * 100 mg/m² intravenous 1 60 minutes
etoposide * 200 mg/m² Once daily oral administration 2, 3
CYCLOPHOSPHamide 750 mg/m² intravenous 1 60 minutes
pegFILGRASTIM 6 mg subcutaneous injection 4

If for stem cell harvest, mobilise as per institutional practice.

Full details

Cycles 1 to 6 - 14 days

Day: 1

Medication Dose Route Max duration Details
prEDNISone 100 mg flat dosing Once daily oral administration
Instructions:
Take in the morning with food.
DOXOrubicin * 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.
vinCRISTine 1.4 mg/m² Cap dose per administration at: 2 mg intravenous 10 minutes
Instructions:
  • Diluted in a minibag.
  • FOR INTRAVENOUS USE ONLY – fatal if given by any other routes.
  • 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) * 100 mg/m² intravenous 60 minutes
CYCLOPHOSPHamide 750 mg/m² intravenous 60 minutes

Day: 2

Medication Dose Route Max duration Details
prEDNISone 100 mg flat dosing Once daily oral administration
Instructions:
Take in the morning with food.
etoposide * 200 mg/m² Once daily oral administration
Instructions:

Take each dose on an empty stomach - one hour before OR two hours after food. Grapefruit or grapefruit juice may interact with this medicine, discuss with your pharmacist.

Round dose to closest multiple of 50 mg and/or 100 mg capsules.

Day: 3

Medication Dose Route Max duration Details
prEDNISone 100 mg flat dosing Once daily oral administration
Instructions:
Take in the morning with food.
etoposide * 200 mg/m² Once daily oral administration
Instructions:

Take each dose on an empty stomach - one hour before OR two hours after food. Grapefruit or grapefruit juice may interact with this medicine, discuss with your pharmacist.

Round dose to closest multiple of 50 mg and/or 100 mg capsules.

Day: 4

Medication Dose Route Max duration Details
prEDNISone 100 mg flat dosing Once daily oral administration
Instructions:
Take in the morning with food.
pegFILGRASTIM 6 mg subcutaneous injection

Day: 5

Medication Dose Route Max duration Details
prEDNISone 100 mg flat dosing Once daily oral administration
Instructions:
Take in the morning with food.

Supportive Care Factors

Factor Value
Antiviral prophylaxis for herpes virus: Routine antiviral prophylaxis may be considered
Constipation risk: laxatives are usually prescribed
Emetogenicity: Medium
Gastroprotection: Gastroprotection may be considered
Growth factor support: Recommended for primary prophylaxis
Pneumocystis jirovecii pneumonia (PJP) prophylaxis: Routine antibiotic prophylaxis recommended
Tumour lysis syndrome prophylaxis: Tumour lysis syndrome prophylaxis is recommended

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.

Tumour lysis syndrome prophylaxis: Recommended for cycle 1 and consider for subsequent cycles.

References

Savage, K. J., M. Chhanabhai, R. D. Gascoyne, et al. 2004. "Characterization of peripheral T-cell lymphomas in a single North American institution by the WHO classification." Ann Oncol 15(10):1467-1475. , PMID: 15367405

Vose, J., J. Armitage, D. Weisenburger, et al. 2008. "International peripheral T-cell and natural killer/T-cell lymphoma study: pathology findings and clinical outcomes." J Clin Oncol 26(25):4124-4130. , PMID: 18626005

Reimer, P., T. Rudiger, E. Geissinger, et al. 2009. "Autologous stem-cell transplantation as first-line therapy in peripheral T-cell lymphomas: results of a prospective multicenter study." J Clin Oncol 27(1):106-113. , PMID: 19029417

Simon, A., M. Peoch, P. Casassus, et al. 2010. "Upfront VIP-reinforced-ABVD (VIP-rABVD) is not superior to CHOP/21 in newly diagnosed peripheral T cell lymphoma. Results of the randomized phase III trial GOELAMS-LTP95." Br J Haematol 151(2):159-166., PMID: 20738307

Schmitz, N., L. Trumper, M. Ziepert, et al. 2010. "Treatment and prognosis of mature T-cell and NK-cell lymphoma: an analysis of patients with T-cell lymphoma treated in studies of the German High-Grade Non-Hodgkin Lymphoma Study Group." Blood 116(18):3418-3425., PMID: 20660290

d'Amore, F., T. Relander, G. F. Lauritzsen, et al. 2012. "Up-front autologous stem-cell transplantation in peripheral T-cell lymphoma: NLG-T-01." J Clin Oncol 30(25):3093-3099. , PMID: 22851556

Link Pharmaceuticals VEPESID® datasheet 18 November 2021 https://www.medsafe.govt.nz/profs/datasheet/v/Vepesidcapinj.pdf (accessed 24 January 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.