Wednesday, September 21, 2016

Zinecard


Generic Name: Dexrazoxane Hydrochloride
Class: Protective Agents
ATC Class: V03AF02
VA Class: AN700
Chemical Name: (S)-4,4′-(1-Methyl-1,2-ethanediyl)bis-2,6-piperazinedione
Molecular Formula: C11H16N4O4
CAS Number: 24584-09-6

Introduction

Cardioprotective agent; a cyclic derivative of edetic acid (EDTA).1 2 3 4 5 6 7 8 9 10 11 13 16 44 45


Uses for Zinecard


Anthracycline-induced Cardiomyopathy Prophylaxis


Reduction of the incidence and severity of cardiomyopathy associated with doxorubicin administration in women with metastatic breast cancer who have received a cumulative doxorubicin dose of ≥300 mg/m2 and would benefit from continued doxorubicin therapy (designated an orphan drug by FDA for this use).1 2 3 4 5 6 7 8 9 10 11 16 44 45 47


Not recommended for use with initiation of doxorubicin therapy.1 2 4 5 16 18 35 39 46 (See Effectiveness of Cytotoxic Regimens under Cautions.)


Zinecard Dosage and Administration


General



  • Consult specialized references for procedures for proper handling and disposal of antineoplastics.1



Administration


IV Administration


Administer by slow IV injection or by rapid IV infusion.1 2 3 4 6 7 8 9 13


Handle cautiously; use protective equipment (e.g., latex gloves).1


Administer dexrazoxane ≤30 minutes prior to initiating doxorubicin therapy; administer doxorubicin no later than 30 minutes after the start of dexrazoxane administration.1 2 3 4 5 6 7 8 9 10 11 46 Do not administer doxorubicin prior to dexrazoxane.a


Reconstitution

Reconstitute vial containing 250 or 500 mg of dexrazoxane powder with 25 or 50 mL of (1/6) M sodium lactate injection (provided by manufacturer), respectively, to provide a solution containing 10 mg/mL.1


Dilution

May be further diluted with 0.9% sodium chloride injection or 5% dextrose injection to a concentration of 1.3–5 mg/mL.a 1


Rate of Administration

Administer by slow IV push or rapid IV infusion over 5–15 minutes.a 1 2 3 4 6 7 8 9 13


Dosage


Available as dexrazoxane hydrochloride; dosage expressed in terms of dexrazoxane.a 1


Administer in a dosage ratio relative to the IV dose of doxorubicin hydrochloride.1


Adults


Prophylaxis of Anthracycline-induced Cardiomyopathy

IV

Recommended dosage ratio of dexrazoxane to doxorubicin is 10:1 (e.g., 500 mg/m2 dexrazoxane should be administered with 50 mg/m2 doxorubicin).1 2 4 5 8 9 13 44


Prescribing Limits


Adults


Prophylaxis of Anthracycline-induced Cardiomyopathy

IV

Maximum 1000 mg/m2 every 3 weeks was administered during clinical trials.a


Special Populations


Hepatic Impairment


Reduced doxorubicin dose recommended in patients with hyperbilirubinemia; proportionally reduce dexrazoxane dosage maintaining 10:1 dexrazoxane to doxorubicin ratio.a


Renal Impairment


Moderate to severe renal impairment (Clcr <40 mL/min): Reduce dosage ratio to 5:1 dexrazoxane to doxorubicin (e.g., 250 mg/m2 dexrazoxane if 50 mg/m2 doxorubicin is administered).a


Not studied in those undergoing dialysis.a


Geriatric Patients


No dosage adjustments except those related to renal impairment.a (See Renal Impairment under Dosage and Administration.)


Cautions for Zinecard


Contraindications


Use with chemotherapy regimens that do not contain an anthracycline.a


Warnings/Precautions


Warnings


Hematologic Effects

May add to myelosuppression caused by chemotherapeutic agents; perform CBCs frequently.a


Effectiveness of Cytotoxic Regimens

Concurrent use of dexrazoxane with the initiation of fluorouracil, doxorubicin, and cyclophosphamide (FAC) therapy may interfere with the antitumor efficacy of the regimen; such use is not recommended.a (See Prophylaxis of Anthracycline-induced Cardiotoxicity under Uses.)


Cardiotoxicity

Use of dexrazoxane does not eliminate potential for anthracycline induced cardiac toxicity; monitor cardiac function carefully.a


Secondary Malignancies

Possible increased risk of secondary malignancies; acute myeloid leukemias, lymphomas, and cutaneous carcinomas reported in patients treated chronically with oral razoxane, a racemic mixture of which dexrazoxane is the S(+)-enantiomer.a


Specific Populations


Pregnancy

Category C.


Lactation

Not known whether dexrazoxane is distributed into milk.a Discontinue nursing because of potential risk to nursing infants.a


Pediatric Use

Safety and efficacy not established.a


Geriatric Use

Response in patients >65 years of age does not appear to differ from that in younger adults; however, use with caution due to greater frequency of decreased hepatic, renal, and/or cardiac function and of concomitant disease and drug therapy observed in the elderly.a


Hepatic Impairment

Pharmacokinetics not evaluated; dosage adjustments may be required in patients with hyperbilirubinemia.a (See Hepatic Impairment under Dosage and Administration.)


Renal Impairment

Decreased clearance; dosage adjustments necessary in patients with moderate to severe renal impairment (Clcr <40 mL/min).a (See Renal Impairment under Dosage and Administration.)


Common Adverse Effects


Alopecia, nausea, vomiting, fatigue/malaise, anorexia, stomatitis, fever, infection, diarrhea, pain on injection, sepsis, neurotoxicity.a


Interactions for Zinecard


Antineoplastic Agents


No significant change in pharmacokinetics of doxorubicin and its predominant metabolite reported with concurrent use of dexrazoxane.a


Zinecard Pharmacokinetics


Distribution


Extent


Distributed primarily in total body water.a


Plasma Protein Binding


Not bound to plasma proteins.a


Elimination


Metabolism


Metabolized to a diacid-diamide cleavage product and two monoacid-monoamide ring products.a


Elimination Route


Excreted principally in urine as unchanged drug (42%), a diacid-diamide cleavage product, and two monoacid-monoamide ring products.a


Half-life


2.1–2.5 hours.a


Stability


Storage


Parenteral


Injection

25°C (may be exposed to 15–30°C).a 1


Reconstituted or diluted solutions are stable for 6 hours at 15–30°C or under refrigeration (2–8°C).1


Discard unused solutions.1


Compatibility


For information on systemic interactions resulting from concomitant use, see Interactions.


Parenteral


Solution CompatibilityHID





Compatible



Dextrose 5% in water



Sodium chloride 0.9%


Drug CompatibilityHID





Y-Site Compatibility

Compatible



Gemcitabine HCl



Pemetrexed disodium


ActionsActions



  • Cardioprotective agent that readily penetrates cell membranes; however, exact mechanism of cardioprotective effect not clearly established.a




  • Converts intracellularly to a ring-opened bidentate chelating agent that may prevent anthracycline-induced cardiotoxicity, at least in part, by chelating free iron and thus preventing the formation of the anthracycline-iron complex and resultant free radical generation.a 1 2 3 4 5 7 11 13 16 38 40 42



Advice to Patients



  • Importance of recognizing and reporting signs and symptoms of CHF.a




  • Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as any concomitant illnesses.a




  • Importance of women informing their clinician if they are or plan to become pregnant or plan to breast-feed.a




  • Importance of informing patients of other important precautionary information. (See Cautions)



Preparations


Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.


















Dexrazoxane Hydrochloride

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Parenteral



For injection, for IV use



250 mg (of dexrazoxane)



Zinecard (with 25 mL sodium lactate injection 0.167 Molar [M/6] diluent)



Pfizer



500 mg (of dexrazoxane)



Zinecard (with 50 mL sodium lactate injection 0.167 Molar [M/6] diluent)



Pfizer



Disclaimer

This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.


The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.

AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions September 2007. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.




References



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2. Anon. Dexrazoxane. Phase III Drug Profiles. 1993; 3:20-7.



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40. Hasinoff BB. NADPH-cytochrome-P450 reductase promotes hydroxyl radical production by the iron complex of ADR-925, the hydrolysis product of ICRF-187 (dexrazoxane). Free Radical Res. 1995; 22:319-25.



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a. Pharmacia & Upjohn Co. Div. of Pfizer, Inc. Zinecard (dexrazoxane) for injection prescribing information. New York, NY; 2004 Oct.



HID. Trissel LA. Handbook on injectable drugs. 14th ed. Bethesda, MD: American Society of Health-System Pharmacists; 2007:496.



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