Haematology / Page 1 of 5
Burkitt-type Lymphoma
Hyper-CVAD
This alternates with MTX Ara C / Height / cm
Weight / kg
BSA / m2
Cycle length: / 21 days / CBC / Day 1 / Limits / Allergies/Hypersensitivities:
Antiemetics
± domperidone 10-20mg PO QID
± Lorazepam 1-2mg PO daily / Agent
Rituximab days 1 and 11 for 1st4 cycles
Cyclophosphamide days 1-4 Q12H
Vincristine days 4 and 11 (2 doses)
Doxorubicin day 4
Dexamethasone days 1-4 and 11-14
DOSE MODIFIED:NO YESNOYES / Round
10 mg
20mg
0.2mg
5mg
Cycle no / 1 3 / Date
Destination / Neuts / ≥3 X 109/L
Plts / ≥50X 109/L
Reference:Thomas et al Cancer, 2006106(7) 1569-1580
Day / Date / Time / Agent / Dose / Route / Instructions / Doctor / Nurse / Check / Start / Stop
-1 / Methotrexate 12mg IT / See intrathecal chemotherapy chart
1 / *Methylprednisone / 100 / mg / IV / In 100ml 0.9% saline over 15 mins
*Paracetamol / 1000 / mg / PO / 30-60 minutes prior to rituximab
*Loratidine / 20 / mg / PO / 30-60 minutes prior to rituximab
*Rituxumab 375mg/m2 / mg / IV / Standard infusion: added to 500 ml 0.9S
Rapid infusion: added to 500ml 0.9S
1-4 / Dexamethasone daily for 4 days / 40 / mg / PO / (days 1-4 and 11-14) Prescribe on QMR4/outpatient script
1 / Ondansetron / 8 / mg / PO / Give 30-60 minutes prior to chemo
T =0 / Cyclophosphamide 300mg/m2 / mg / IV / In 100ml D5W over 2 hours Q12H
T =0 / MESNA 600mg/m2 / mg / IV / In 500ml D5W over 24 hrs

* Rituximab is given for the first 4 cycles only– 8 doses. See rituximab recording chart Page 4

  • Give IV hydration with alkalinisation and allopuinol ( or rasbuicase for high tumour burden) during course 1. Encourage patients to drink at least 3 litres of fluid per day, and to void frequently when receiving cyclophosphamide.Cyclophosphamide and mesna are infused via a Y-site connector
  • Hyper CVAD consists of 2 regimes – Hyper CVAD and High dose Methotrexate and Cytarabine Arabinoside. Both regimes are given 21 days apart.8 cycles are usually given.
  • CNS prophylaxis is given with each cycle total of 16 treatments. If CNS disease, IT therapy is given twice weekly until CSF cell count normalised and cytology negative.

Patient Category:
Y J A P O 1 3 Z / OSP Group:
1 2 3 4 5 6 7 / Consultant:
NZMC Reg. No: / Special authority:
Rituximab
Burkitt-type Lymphoma
Hyper-CVAD
This alternates with MTX Ara C / Height / cm
Weight / kg
BSA / m2
Day / Date / Time / Agent / Dose / Route / Instructions / Doctor / Nurse / Check / Start / Stop
1 / Ondansetron / 8 / mg / PO / Give 30-60 minutes prior to chemo
T +12h / Cyclophosphamide 300mg/m2 / mg / IV / In 100ml D5Wover 2 hours Q12H
2 / Ondansetron / 8 / mg / PO / Give 30-60 minutes prior to chemo
T =0 / Cyclophosphamide 300mg/m2 / mg / IV / In 100ml D5W over 2 hours Q12H
T =0 / MESNA 600mg/m2 / mg / IV / In 1000ml D5W over 24 hrs
Ondansetron / 8 / mg / PO / Give 30-60 minutes prior to chemo
T +12h / Cyclophosphamide 300mg/m2 / mg / IV / In 100ml D5W over 2 hours Q12H
3 / Ondansetron / 8 / mg / PO / Give 30-60 minutes prior to chemo
T =0 / Cyclophosphamide 300mg/m2 / mg / IV / In 100ml D5W over 2 hours Q12H
T =0 / MESNA 600mg/m2 / mg / IV / In 1000ml D5W over 24 hrs
Ondansetron / 8 / mg / PO / Give 30-60 minutes prior to chemo
T +12h / Cyclophosphamide 300mg/m2 / mg / IV / In 100ml D5W over 2 hours Q12H
4 / Vincristine 1.4mg/m2 / mg / IV / In 50ml 0.9S free run over 10 mins
0.9% Sodium Chloride / 250 / ml / IV / Flush and fast running saline
Doxorubicin 50mg/m2 / mg / IV / In 500ml 0.9% saline over 24 hrs
Pegylated G-CSF / 6 / mg / SC / 24 hours following last dose of chemotherapy.
  • Doxorubicin must be given via a CVAD

Burkitt-type Lymphoma
Hyper-CVAD
This alternates with MTX Ara C / Height / cm
Weight / kg
BSA / m2
Day / Date / Time / Agent / Dose / Route / Instructions / Doctor / Nurse / Check / Start / Stop
8 / Cytarabine 100mg IT / See intrathecal chemotherapy chart
11 / *Methylprednisone / 100 / mg / IV / In 100ml 0.9% saline over 15 mins
*Paracetamol / 1000 / mg / PO / 30-60 minutes prior to rituximab
*Loratidine / 20 / mg / PO / 30-60 minutes prior to rituximab
*Rituxumab 375mg/m2 / mg / IV / Standard infusion: added to 500 ml 0.9S
Rapid infusion: added to 500ml 0.9S
11 / Vincristine 1.4mg/m2 / mg / IV / In 50ml 0.9S free run over 10 mins
0.9% Sodium Chloride / 100 / ml / IV / For flushing
11-14 / Dexamethasone daily for 4 days / 40 / mg / PO / Chart on QMR4 or give OP Script

* Rituximab is given for the first 4 cycles only– 8 doses. See rituximab recording chart Page 5

Authorised by Dr S Gibbons Pharmacist: B Harden / February 2015
T:\Pictures\CDHB\Red_Book\NHL Burkitt-type lymphoma Ritux hyper-CVAD cycles 1 and 3.docx / Review: 2016
CHEMOTHERAPY
MEDICATION
CHART
C260070

Haematology / Page 1of 5
Rituximab (Mabthera®) giving instructions
Patient label
Date

Standard infusion:

/ Commence infusion at 50 mg/hr for the first hour, if no side effects; increase the infusion rate in 50mg increments every 30 minutes to a maximum rate of 400mg/hr. Remember that the IV line will have been primed with saline therefore rituximab will not be infused immediately.
To calculate 50mg in _____ml
Rapid infusion: / If no previous toxicities, give 20% of the dose over 30 minutes and the remaining 80% over the following 60 minutes.
If any adverse effects noted: / Discontinue infusion, evaluate severity of symptoms, and treat accordingly. If reactions settle, recommence at ½ the previous rate. Consider hydrocortisone 100mg IV if required, plus chlorphenamine and paracetamol depending on time interval.
Document recordings – T,P,R,B/P and EWS on adult observation chart
Following infusion: Observe for delayed side effects, for 2 hours following infusion.
Time / Rate / Comments
Baseline
30 mins
45 mins
60 mins
75 mins
2 hours
3 hours
4 hours
5 hours

Note:•Monitor patients with high tumour burden for infusion related reactions and tumour lysis syndrome.

•Ensure adequate hydration and consider addition of allopurinol for 1 – 3 courses.

DO NOT SHAKE during preparation, rotate gently. Aggregation & precipitation of antibody can occur.

PRN medications for Hypersensitivity reactions

Date / Time / Medication / Dose / Route / Doctor / Nurse / Check
Hydrocortisone / 100 mg / Slow IV bolus
Paracetamol / 1000 mg / PO
Chlorphenamine / 10 mg / Slow IV bolus
PRN antiemetics / DR / NURSE SIGN
Domperidone / 10-20 mg / PO QID
Cyclizine / 50 mg / PO/IV Q8H
Lorazepam / 0.5-1 mg / PO BD
Rituximab (Mabthera®) giving instructions
Patient label
Date

Standard infusion:

/ Commence infusion at 50 mg/hr for the first hour, if no side effects; increase the infusion rate in 50mg increments every 30 minutes to a maximum rate of 400mg/hr. Remember that the IV line will have been primed with saline therefore rituximab will not be infused immediately.
To calculate 50mg in _____ml
Rapid infusion: / If no previous toxicities, give 20% of the dose over 30 minutes and the remaining 80% over the following 60 minutes.
If any adverse effects noted: / Discontinue infusion, evaluate severity of symptoms, and treat accordingly. If reactions settle, recommence at ½ the previous rate. Consider hydrocortisone 100mg IV if required, plus chlorphenamine and paracetamol depending on time interval.
Document recordings – T,P,R,B/P and EWS on adult observation chart
Following infusion: Observe for delayed side effects, for 2 hours following infusion.
Time / Rate / Comments
Baseline
30 mins
45 mins
60 mins
75 mins
2 hours
3 hours
4 hours
5 hours

Note:•Monitor patients with high tumour burden for infusion related reactions and tumour lysis syndrome.

•Ensure adequate hydration and consider addition of allopurinol for 1 – 3 courses.

DO NOT SHAKE during preparation, rotate gently. Aggregation & precipitation of antibody can occur.

PRN medications for Hypersensitivity reactions

Date / Time / Medication / Dose / Route / Doctor / Nurse / Check
Hydrocortisone / 100 mg / Slow IV bolus
Paracetamol / 1000 mg / PO
Chlorphenamine / 10 mg / Slow IV bolus
PRN antiemetics / DR / NURSE SIGN
Domperidone / 10-20 mg / PO QID
Cyclizine / 50 mg / PO/IV Q8H
Lorazepam / 0.5-1 mg / PO BD
Authorised by Dr S GibbonsPharmacist B Harden / February 2015
T:\Pictures\CDHB\Red_Book\NHL Burkitt-type lymphoma Ritux hyper-CVAD cycles 1 and 3.docx / Review 2016