Systemic Anti-Cancer Therapy Regimen Library
LEU ALL precursor B-cell - UKALL14 with RITUximab [40 years and under] [for transplant]
Treatment Overview
UKALL14 with RITUximab [40 years and under] [for transplant] is intended for those with 40 years and under with CD20 expression greater than 10%, and a transplant planned.
This regimen consists of:
- Steroid pre-phase
- Phase 1 Induction
- Phase 2 Induction
- Intensification/CNS prophylaxis
- Consolidation [Cycles 1 and 2]
- Consolidation/delayed intensification [Cycle 3] Day 29 of this cycle should be delayed, if necessary, until count recovery.
- Consolidation [Cycle 4]
Each Cycle/phase starts after count recovery from the previous Cycle/phase with:
- Neutrophils greater than 0.75 x 109/L, and
- Platelets greater than 75 x 109/L.
Intrathecal metHOTREXATe, as per regimen is for CNS prophylaxis, escalation to a treatment strategy will be required for CNS disease or traumatic lumbar puncture.
dexamethasone pre-phase can be given for 5 to 7 days.
Followed by:
Starts after count recovery from Phase 1 Induction.
Starts after count recovery from Phase 2 Induction.
Consolidation Cycle 1 starts after count recovery from Intensification/CNS prophylaxis.
Cycle 2 is given on count recovery from Cycle 1.
Starts after count recovery from Consolidation Cycle 2.
Day 29 of this cycle should be delayed, if necessary, until count recovery.
Starts after count recovery from Consolidation/delayed intensification Cycle 3.
Supportive Care Factors
| Factor | Value |
|---|---|
| Antifungal prophylaxis: | Routine antifungal prophylaxis recommended |
| Antiviral prophylaxis for hepatitis B virus: | Required for anti–HBc positive patients at risk of reactivation |
| Antiviral prophylaxis for herpes virus: | Routine antiviral prophylaxis recommended |
| Constipation risk: | Variable |
| Emetogenicity: | Variable |
| Folinic acid rescue for high dose methotrexate: | Variable |
| Gastroprotection: | Variable |
| Hydration: | Variable |
| Hypersensitivity / Infusion related reaction risk: | Variable |
| Pneumocystis jirovecii pneumonia (PJP) prophylaxis: | Routine antibiotic prophylaxis recommended |
| Tumour lysis syndrome prophylaxis: | Variable |
Gastroprotection: Gastroprotective agents are only intended for short term use while patient is receiving corticosteroid treatment doses.
References
Cancer Research UK and University College London, UKALL14 A randomized trial for adults with newly diagnosed acute lymphoblastic leukaemia Clinicaltrials.gov no: NCT01085617 Version 5.0 20.07.12 Accessed 16 September 2022.
Servier Laboratories NZ Ltd Oncaspar®New Zealand data sheet 25 August 2022 https://www.medsafe.govt.nz/profs/datasheet/o/oncasparinj.pdf (accessed 7 February 2023).
Clinical Commissioning Policy: Addition of rituximab to first-line standard chemotherapy for CD20 positive B-cell precursor acute lymphoblastic leukaemia (Adults) Publication date: January 2021 Version number: 1.0 https://www.england.nhs.uk/wp-content/uploads/2021/01/1748-Addition-of-rituximab-to-first-line-standard-chemotherapy-for-CD20-positive-B-cell-precursor-acute-lympho.pdf (accessed 14 October 2022).
Medicines and Hepatitis B Reactivation Prescriber Update 38(1): 2-3 March 2017 https://medsafe.govt.nz/profs/PUArticles/March2017/MedicinesAndHepatitisB.htm.
Rituximab and Hepatitis B Reactivation Prescriber Update 34(3):27 September 2013 https://www.medsafe.govt.nz/profs/PUArticles/Sept2013RituximabHepB.htm.
Regimen details sometimes vary slightly from the published literature after recommendation by expert committee consensus.
* 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.