Anthracyclines Flashcards

1
Q

Name the 4

A

Daunorubicin
Doxorubicin hydrochloride
Epirubicin hydrochloride
Idarubicin hydrochloride

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2
Q

Name the 2 anthracycline derivative

A

Mitoxantrone
Pixantrone

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3
Q

Which 2 are available as both conventional and liposomal formulations

A

Doxorubicin, daunorubicin

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4
Q

Which complication is most often associated with FU, MTX and anthracyclines?

A

oral mucositis

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5
Q

What is a main important SE that they are associated with

A

dose-related, cumulative and potenitally life threatening cardiotoxic SE

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6
Q

Are conventional and pegylated liposomal formulations of doxorubicin, daunorubicin interchangeable

A

NO

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7
Q

Important safety info- doxorubicin & daunorubicin re liposomal and lipid-complex formulations name change to reduce medication errors

A
  • serious harm and fatal overdoses have occured due to mix up between the different forms
  • therefore medicines now will explicitly inlude ‘liposomal’, ‘pegylated-liposomal’, or ‘lipid complex’ within their name to reduce risk of potentially fatal medical errors
  • they are not interchangeable
  • clear distinction between forms required when prescribing, dispensing, administering, communicating about doxorubicin
  • verify produce name and dose before admin and do not exceed max dose
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8
Q

Caution is necessary with the concurrent use of anthracyclines and ….. drugs

A

cardiotoxic drugs, or drugs that reduce cardiac contracility

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9
Q

Where is doxorubicin largely excreted?

A

Bile

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10
Q

What is the significance of bilirubin concentrations with doxorubicin?

A

Doxorubicin is largely excreted in the bile and an elevated bilirubin concentration is an indication for reducing the dose.

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11
Q

Doxorubicin & cardiomyopathy - doses

A

Higher cumulative doses are associated with cardiomyopathy and it is usual to limit total cumulative doses to 450 mg/m2.

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12
Q

What are the adv and disadv of liposomal forms of doxorubicin

A
  • they may reduce incidence of cardiotoxicity and lower the potential for local necrosis
  • however infusion rwactions, sometimes severe may occur
  • hand-foot syndrome (painful, macular reddening skin eruptions) occurs commonly with liposomal doxorubucin and may be dose limiting
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13
Q

What is hand-foot syndrome, what drug does it most often occur with and how can it be prevented

A

Hand-foot syndrome (painful, macular reddening skin eruptions) occurs commonly with liposomal doxorubicin and may be dose limiting.
It can occur after 2–3 treatment cycles and may be prevented by cooling hands and feet and avoiding socks, gloves, or tight-fitting footwear.
It may also occur with non-liposomal formulations.

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14
Q

Conception & contraception advice with doxorubicin

A

effective contraception during and for at least 6 months after treatment in men or women.

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15
Q

Cardiac contraindications include

A
  • myocardiopathy
  • recent MI
  • severe arrhythmia
  • severe myocardial insufficiency
  • unstable angina
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16
Q

epirubicin - conception and contraception advice

A

Females of childbearing potential should use effective contraception during treatment and for at least 6.5 months after last dose; male patients should use effective contraception during treatment and for at least 3.5 months after last dose.

17
Q

Epirubicin doses & congestive HF

A

Manufacturer advises extreme caution with cumulative doses exceeding 900 mg/m2—risk of congestive heart failure increased.

18
Q

daunorubicin & cardiotoxicity

A

Cardiotoxicity is cumulative and may be irreversible, however responds to treatment if detected early.

19
Q

CI of all anthracyclines re previous treatment with anthracyclines

A

Contraindicated if pt has had previous treatment with maximum cumulative dose of anthracycline

20
Q

Idarubicin conception and contraception advice

A

Females of childbearing potential should use effective contraception during treatment and for at least 6 and a half months after last treatment; male patients should use effective contraception during treatment and for at least 3 and a half months after last treatment.

21
Q

Is cardiac toxicity still a SE of the 2 anthracycline derivatives mitoxantrone, pixantrone

A

Yes

22
Q

Cardiac toxicity SE – mitoxantrone

A

Cardiac toxicity, including irreversible and fatal congestive heart failure, may occur either during treatment with mitoxantrone or months to years after discontinuation; the risk increases with cumulative dose.

23
Q

Mitoxantrone

A

Manufacturer advises effective contraception during and for at least 6 months after treatment in men or women.

24
Q

CI for pixantrone

A

Active severe infection; risk factors for severe infection

25
Q

Photosensivity is a theoretical risk for this drug and pt should be advised to follow sun protection strategies

A

Pixantrone

26
Q

Photosensivity is a theoretical risk and pt should be advised to follow sun protection strategies for one of the following drugs
- doxorubicin
- daunorubicin
- epirubicin
- pixantrone
- mitocantrone

A
  • pixantrone
27
Q

How to prevent chronic cumulative cardiotoxciity cuased by anthracyclines, and also anthracycline extravasation

(antidote)

A

Dexrazoxane is an antidote - iron chelator

28
Q

name 2 important SE of the antracyclines

A

cardiotoxicity and extravasation injury

reduced by liposomal forms, however they are associated with infusion reactions e.g. hand food syndrome which is likely following doxorubicin liposomal admin after 2-3 treatment cycles

29
Q

patient has cardiotoxicity from anthracycline. what do you do

A

The antidote for anthracyclines is dexrazoxane, which is administered intravenously. Dexrazoxane is used to treat anthracycline-induced cardiotoxicity and extravasation.

30
Q

patient has extravasation injury from anthracycline - tissue necrosis! what do you do

A

The antidote for anthracyclines is dexrazoxane, which is administered intravenously. Dexrazoxane is used to treat anthracycline-induced cardiotoxicity and extravasation.

31
Q

what is dexrazoxane

A

The antidote for anthracyclines is dexrazoxane, which is administered intravenously. Dexrazoxane is used to treat anthracycline-induced cardiotoxicity and extravasation.