Your treatment
The treatment schedule below explains how the drugs for this treatment are given.
R-IVAC (rituximab, ifosfamide, etoposide, cytarabine) | |||
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This treatment protocol alternates withthe dose modified R-CODOX-Mprotocoland may continuefor up to 4 cycles of chemotherapy in total.Your doctor will advise you of the number of treatments you will have. | |||
Day | Treatment | How it is given | How long it takes |
1 | Rituximab(ri-TUX-i-mab) | By a drip into a vein | 1st cycle:About 4 to 6 hours Cycles thereafter:About 3 to 4 hours |
Cytarabine (sye-TARE-a-been) | By a drip into a vein | About 3 hours TWICE a day | |
Etoposide (e-TOE-poe-side) | By a drip into a vein | About 1 hour | |
Mesna(MES-na) | By a drip into a vein | About 15 minutes (day 1 only) | |
Ifosfamide (eye-FOS-fa-mide) | By a drip into a vein | About 2 hours | |
Mesna | By a drip into a vein | For 24 hours | |
2 | Cytarabine | By a drip into a vein | About 3 hours TWICE a day |
Etoposide | By a drip into a vein | About 1 hour | |
Ifosfamide | By a drip into a vein | About 2 hours | |
Mesna | By a drip into a vein | For 24 hours | |
3 and 4 | Etoposide | By a drip into a vein | About 1 hour |
Ifosfamide | By a drip into a vein | About 2 hours | |
Mesna | By a drip into a vein | For 24 hours | |
5 | Etoposide | By a drip into a vein | About 1 hour |
Ifosfamide | By a drip into a vein | About 2 hours | |
Mesna | By a drip into a vein | For 24 hours | |
Methotrexate (meth-o-TREX-ate) | By injection into your spine | About 2 hours | |
6 | Mesna | By a drip into a vein | For 24 hours |
Calcium folinate (Leucovorin) (loo-koe-VOR-in) | Take orally for ONE dose only, 24 hours after the methotrexateinjection. | ||
7 | Granulocyte Colony Stimulating Factor (G-CSF) | By injection under the skin | About 5 minutes |
- After completion of chemotherapy, you may require a further two doses of rituximab. Your doctor will determine whether this is appropriate.
When to get help
Anticancer drugs (drugs used to treat cancer) can sometimes cause serious problems. It is important to get medical help immediately if you become unwell.
| Emergency contact details Ask your doctor or nurse from your treating team who to contact if you have a problem | ||
| Daytime: Night/weekend: Other instructions: |
During your treatment immediately tell the doctor or nurse looking after you if you get any of the following problems:
- leaking from the area where the drugs are being given
- pain, stinging, swelling or redness in the area where the drugs are being givenor at any injection sites
- a skin rash, itching, feeling short of breath, wheezing, fever, shivers, or feeling dizzy or unwell in any way (allergic reaction).
Other information about your treatment
Changes to your dose or treatment delays
Sometimes a treatment may be started at a lower dose or the dose needs to be changed during treatment. There may also be times when your treatment is delayed.This can happen if your doctor thinks you are likely to have severe side effects, if you get severe side effects, if your blood counts are affected andcausing delays in treatment, or if you are finding it hard to cope with the treatment. This is called a dose reduction, dose change or treatment delay. Your doctor will explain if you need any changes or delays to your treatment and the reason why.
Blood tests and monitoring
Anti-cancer drugs can reduce the number of blood cells in your body. You will need to have regular blood tests to check that your blood cell count has returned to normal. If your blood count is low, your treatment may be delayed until it has returned to normal. Your doctor or nurse will tell you when to have these blood tests.
Central venous access devices (CVADs)
Your treatment will be given through a central venous access device (CVAD). Your doctor or nurse will explain this to you.For more information see the eviQ patient information sheets on CVADs.
Medications for blood pressure
Rituximab may lower your blood pressure. Tell your doctor if you are taking any blood pressure medications. Your doctor may advise you to temporarily stop your blood pressure medications before your rituximab infusions.
Other medications given during this treatment
- Rituximab premedication:before your treatment with rituximab you will need to take some tablets called a premedication to help prevent you from having a reaction to the rituximab.
- Anti-sickness (anti-nausea) medication: you may be given some anti-sickness medication.Make sure you take this medicationas your doctor or nurse tells you, even if you don’t feel sick. This can help to prevent the sickness starting.
- Eye drops: you will be given eye drops to help prevent sore eyes. You will start using the eye drops before you have your first dose of cytarabine and continue to use the eye drops until 72 hours after your last dose of cytarabine.
- Prophylaxis medication: youmay need to take some medications to prevent infection and to help prevent or reduce some of the side effects of your treatment. Your doctor or nurse will tell you how and when to take these medications.
- G-CSF: you will be given injection(s) of a drug called G-CSF (also called filgrastim, lipegfilgrastim or pegfilgrastim) under your skin. This helps to boost your white blood cell count. Your white blood cells help to fight infection. Lipegfilgrastim and pegfilgrastim are given once. Filgrastim is given for several days until your white blood cells recover.Follow this link to read more information on how to give this injection.
Side effects
Cancer treatments can cause damage to normal cells in your body, which can cause side effects. Everyone gets different side effects, and some people will have more problems than others.
The table below shows some of the side effects you may get with this treatment. You are unlikely to get all of those listed and you may also get some side effects that have not been listed.
Tell your doctor or nurse about any side effects that worry you. Follow the instructions below and those given to you by your doctor or nurse.
Immediate (onset hours to days) | |
Allergic reaction |
While you are in hospital: Tell your doctor or nurse immediately. After you leave: Contact your doctor or nurse immediately, or go to the nearest hospital Emergency Department. |
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Bone pain after G-CSF injection |
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Flu-like symptoms from cytarabine |
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Brain swelling (encephalopathy) |
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Pain or swelling at injection site (extravasation) |
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Bladder irritation (haemorrhagic cystitis) |
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Headache |
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Nausea and vomiting |
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Nervous system changes from cytarabine |
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Eye problems from cytarabine |
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Taste and smell changes |
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Early (onset days to weeks) | |
Infection risk (neutropenia) |
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Low platelets (thrombocytopenia) |
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Appetite loss (anorexia) |
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Tiredness and lack of energy (fatigue) |
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Kidney damage |
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Mouth pain and soreness (mucositis) |
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Skin rash |
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Late (onset weeks to months) | |
Hair loss (alopecia) |
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Low red blood cells (anaemia) |
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Chemo brain (chemotherapy-related cognitive impairment) |
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Changes in the way your brain works [progressive multifocal leukoencephalopathy (PML)] |
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Delayed (onset months to years) | |
Lung problems |
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General advice for people having cancer treatment
Chemotherapy safety
- Learn how to keep you and your family safe while you are having anticancer drugs.
- See our patient information sheet - Chemotherapy safety at home.
Blood clot risk
- Cancer and anticancer drugs can increase the risk of a blood clot (thrombosis).
- Tell your doctor if you have a family history of blood clots.
- A blood clot can cause pain, redness, swelling in your arms or legs, shortness of breath or chest pain.
- If you have any of these symptoms go to your nearest hospital Emergency Department.
Medications and vaccinations
- Before you start treatment, tell your doctor about any medications you are taking, including vitamins or herbal supplements.
- Don’t stop or start any medications during treatment without talking to your doctor and pharmacist first.
- Paracetamol is safe to take if you have a headache or other mild aches and pains. It is recommended that you avoid taking aspirin, ibuprofen and other anti-inflammatory type medications for pain while you are having treatment. However, if these medications have been prescribed by your doctor, do not stop taking them withoutspeaking with your doctor.
- Vaccinations such as flu and tetanus vaccines are safe to receive while having treatment. Do not have any live vaccines during your treatment or for 6 months after it finishes. If you are unsure, check with your doctor before you have any vaccinations.
- People you live with should be fully vaccinated, including having live vaccines according to the current vaccination schedule. Extra care needs to be taken with hand washing and careful disposal of soiled nappies for infants who have recently received the rotavirus vaccine.
Other medical and dental treatment
- If you go to hospital or any other medical appointment (including dental appointments), always tell the person treating you that you are receiving anticancer drugs.
- Before you have any dental treatment, talk to your doctor.
Diet and food safety
- While you are receiving this treatment, it is important that you try to maintain a healthy diet.
- Grapefruit and grapefruit juice can interact withyour medication and should be avoided while you are on this treatment.
- Speak to your doctor or nurse about whether drinking alcohol is safe with your treatment.
- If you have any concerns about recent weight loss or weight gain or questions about your diet, ask to speak to a dietitian.
- There are some foods that may cause infection in high risk individuals and should be avoided. For further information on foods to avoid and food hygiene please ask for a copy of the Listeria and food brochure.
Fertility
- Some cancer treatments can reduce your fertility. This can make it difficult or impossible to get pregnant or father a child.
- Talk to your doctor or nurse before you start any treatment. Depending on your situation there may be fertility sparing options available to you and/or your partner, discuss these with your doctor or nurse.
Pregnancy and breastfeeding
- Some cancer treatments can be dangerous to unborn babies. Talk to your doctor or nurse if you think there is any chance that you could be pregnant.
- Do not try to get pregnant or father a child during this treatment. Contraception should be used during treatment and after stopping treatment. Ask your doctor or nurse about what type of contraception you should use.
- If you are planning pregnancy/fatherhood after completing this treatment, talk to your doctor. Some doctors advise waiting between 6 months and 2 years after treatment.
- Do not breastfeed if you are on this treatment, as anti-cancer medications can also pass into breast milk.
Sex life and sexuality
- The desire to have sex may decrease as a result of this treatment or its side effects.
- Your emotions and the way you feel about yourself may also be affected by this treatment.
- It may help to discuss your concerns with your partner anddoctor or nurse.
Risk of developing a second cancer
- Some anticancer treatments can increase your chance of developing a second cancer, this is rare. Your doctor will discuss with you the specific risks of your treatment.
Quitting smoking
- It is never too late to quit smoking. Quitting smoking is one of the best things you can do to help your treatment work better.
- There are many effective tools to improve your chances of quitting.
- Talk to your treating teamfor more information and referral to a smoking cessation support service.
Staying active
- Research shows that exercise, no matter how small, has many benefitsfor people during and after cancer treatment.
- Talk to your doctor before starting an exercise program. Your doctor can advisewhether you need a modified exercise program.
For more information about cancer treatment, side effects and side effect management see our Patient and carerssection.
Where to get more information
Telephone support
- Call Cancer Council on 13 11 20 for cancer information and support
- Call the Leukaemia Foundation on 1800620420(MontoFri9am – 5pm)
- Call the Lymphoma Nurse Support Line on 1800 953 081 (Mon to Fri 9am - 5pm)
- Call the Myeloma Australia Support Line on 1800 693 566 (Mon to Fri 9am - 5pm)
Haematology,transplant and cellular therapyinformation
- Arrowbonemarrowtransplantfoundation– arrow.org.au
- AustralasianMenopauseSociety– menopause.org.au
- Chris O'Brien Lifehouse- Total Body Irradiation -mylifehouse.org.au/departments/radiation-oncology/total-body-irradiation/
- Healthy Male Andrology Australia –healthymale.org.au/
- International Myeloma Foundation – myeloma.org
- LeukaemiaFoundation –leukaemia.org.au
- LymphomaAustralia– lymphoma.org.au
- Myeloma Australia – myeloma.org.au
- NSWAgencyforClinicalInnovation,Blood&MarrowTransplantNetwork –aci.health.nsw.gov.au/networks/bmtct
- NSW Agency for Clinical Innovation- aci.health.nsw.gov.au/projects/immune-effector-cell-service
- NCCNGuidelines for Patients Immunotherapy Side Effects:CAR T-Cell Therapy - nccn.org/patientresources/patient-resources/guidelines-for-patients
- TalkBloodCancer – cmlsupport.org.uk/organisation-type/social-media-groups
General cancer information and support
- Australian Rare Cancer (ARC) Portal –arcportal.org.au/
- Beyond Blue – beyondblue.org.au
- Cancer Australia – canceraustralia.gov.au
- Cancer Council Australia– cancer.org.au
- Cancer Voices Australia – cancervoicesaustralia.org
- CanTeen – canteen.org.au
- Carers Australia – carersaustralia.com.au
- Carer Help -carerhelp.com.au
- eviQ Cancer Treatments Online–eviQ.org.au
- Is a clinical trial an option for me? -cancer.nsw.gov.au/about-cancer/document-library/i-have-cancer-is-a-clinical-trial-an-option-for-me
- Food Standards Australia New Zealand: Listeria & Food Safety – foodstandards.gov.au/publications/listeriabrochuretext
- LGBTQI+ People and Cancer - cancercouncil.com.au/cancer-information/lgbtqi
- Look Good Feel Better– lgfb.org.au
- Patient Information -patients.cancer.nsw.gov.au
- Radiation Oncology Targeting Cancer - targetingcancer.com.au
- Redkite – redkite.org.au
- Return Unwanted Medicines – returnmed.com.au
- Staying active during cancer treatment –patients.cancer.nsw.gov.au/coping-with-cancer/physical-wellbeing/staying-active
Quit smoking information and support
Quitting smoking is helpful even after you have been diagnosed with cancer. The following resources provide useful information and support to help you quit smoking. Talk to your treating team about any other questions you may have.
- Call Quitline on 13 QUIT (13 78 48)
- iCanQuit – iCanQuit.com.au
- Patient Information -patients.cancer.nsw.gov.au/coping-with-cancer/physical-wellbeing/quitting-smoking
- Quitnow – quitnow.gov.au