Names and pronunciation
(dox-oh-roo′bi-sin) Adriamycin
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Individual generic drug information
Extracted information for DOXOrubicin only.
(dox-oh-roo′bi-sin) Adriamycin
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Func. class.: Antineoplastic, antibiotic
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Chem. class.: Anthracycline glycoside
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Do not confuse: DOXOrubicin/DOXOrubicin liposomal/ DAUNOrubicin
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ACTION: Inhibits DNA synthesis primar- ily; replication is decreased by binding to DNA, which causes strand splitting; active throughout entire cell cycle; a vesicant
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USES: Wilms’ tumor; bladder, breast, lung, ovarian, stomach, thyroid cancer; Hodgkin’s/non-Hodgkin’s disease; acute lymphoblastic leukemia; myeloblastic leukemia; neuroblastomas; soft tissue/ bone sarcomas
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Extracted information for DOXOrubicin only.
CONTRAINDICATIONS: Preg- nancy, breastfeeding, hypersensitivity, systemic infections, cardiac disorders, severe myelosuppression, lifetime dose of 550 mg/m2, hepatic disease Precautions: Accidental exposure, car- diac disease, dental work, electrolyte imbalance, infection, hyperuricemia
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Black Box Warning: Bone marrow sup- pression, extravasation, heart failure, secondary malignancy; requires an expe- rienced clinician, IM/SUBCUT use Black Box Warning: Do not give IM, SUBCUT Black Box Warning: If extravasation oc- curs, stop infusion and complete via an- other vein, preferably in another limb, use dexrazoxane topically • Aluminum needles may be used dur- ing administration; avoid aluminum dur- ing storage • Rapid injection can cause facial flush- ing or erythema along the vein Reconstitution: • To avoid risks with reconstitution, the commercially available injection may be used; there are still risks involved in handling the injection • Do not use diluents containing preser- vatives to reconstitute powder for injection • Reconstitute 10, 20, 50, 100 mg of DOXOrubicin with 5, 10, 25, 50 mL, respectively, of nonbacteriostatic NS in- jection (2 mg/mL), shake until com- pletely dissolved; use reconstituted so- lution within 24 hr; do not expose to sunlight • IV injection Inject reconstituted solution over >3-5 min via Y-site or 3-way stopcock into a free-flow- ing IV infusion of NS or D5W; a butterfly needle inserted into a large vein is preferred • Increase fluid intake to 2-3 L/day to prevent urate, calculi formation • Store at room temperature for 24 hr after reconstituting Y-site compatibilities: Alemtuzumab, alfentanil, amifostine, amikacin, anidula- fungin, argatroban, aztreonam, bivalirudin, bleomycin, bumetanide, buprenorphine, butorphanol, calcium chloride/gluconate, CARBOplatin, car- mustine, caspofungin, ceftizoxime, chlor- proMAZINE, cimetidine, ciprofloxacin, CISplatin, cladribine, clindamycin, cyclo- phosphamide, cycloSPORINE, cytara- bine, DACTINomycin, DAPTOmycin, dexamethasone, diltiazem, diphenhydrA MINE, DOBUTamine, DOCEtaxel, dolase- tron, DOPamine, doripenem, doxycy- cline, droperidol, enalaprilat, ePHEDrine, EPINEPHrine, erythromycin, esmolol, etoposide, etoposide phos- phate, famotidine, fenoldopam, fentaNYL, filgrastim, fluconazole, fludarabine, gem- citabine, gentamicin, granisetron, halo- peridol, hydrocortisone, HYDROmor- phone, ifosfamide, imipenem cilastatin, inamrinone, isoproterenol, ketorolac, labetalol, leucovorin, levorphanol, lido- caine, linezolid, LORazepam, mannitol, mechlorethamine, melphalan, meperi- dine, mesna, methotrexate, metoclo- pramide, metoprolol, metroNIDAZOLE, midazolam, milrinone, mitoMYcin, mor- phine, nalbuphine, naloxone, nesiritide, niCARdipine, nitroglycerin, nitroprus- side, octreotide, ofloxacin, ondansetron, oxaliplatin, PACLitaxel, palonosetron, pancuronium, phenylephrine, potassium chloride, procainamide, prochlorpera- zine, promethazine, propranolol, quinu- pristin-dalfopristin, ranitidine, sar- gramostim, sodium acetate, tacrolimus, teniposide, theophylline, thiotepa, ticar- cillin/clavulanate, tigecycline, tirofiban, tobramycin, topotecan, trastuzumab, tri- methobenzamide, vancomycin, vasopres- sin, vecuronium, verapamil, vinBLAStine, vinCRIStine, vinorelbine, zidovudine, zoledronic acid Black Box Warning: Bone marrow de- pression: CBC, differential, platelet count weekly; withhold or reduce dose of product if WBC is <1500/mm3 or platelet count is <50,000/mm3; notify prescriber of these results • Renal studies: BUN, serum uric acid, urine CCr, electrolytes prior to, during therapy • I&O ratio: report fall in urine output to <30 mL/hr • Monitor temperature: fever might in- dicate beginning infection • Hepatotoxicity: hepatic studies prior to, during therapy: bilirubin, AST, ALT, alka- line phosphatase as needed or monthly; check for jaundice of skin and sclera, dark urine, clay-colored stools, itchy skin, abdominal pain, fever, diarrhea Black Box Warning: Dysrhythmias: ECG; watch for ST-T wave changes, low QRS and T, possible dysrhythmias (sinus tachycardia, heart block, PVCs), ejection fraction prior to treatment, signs of irre- versible cardiomyopathy, can occur up to 6 mo after treatment begins • Bleeding: hematuria, guaiac, bruising, petechiae of mucosa or orifices every 8 hr • Effects of alopecia on body image; discuss feelings about body changes; al- most total alopecia is expected • Buccal cavity every 8 hr for dryness, sores, ulceration, white patches, oral pain, bleeding, dysphagia • Alkalosis if severe vomiting is present Black Box Warning: Secondary malig- nancy: assess for AML and MDS, which may occur Black Box Warning: Extravasation: lo- cal irritation, pain, burning at injection site; a vesicant; if extravasation occurs, stop drug, restart at another site, apply ice, elevate extremity to reduce swelling; if resolution does not occur, surgical de- bridement may be required • GI symptoms: frequency of stools, cramping • Rinsing of mouth tid-qid with water, club soda; brushing of teeth bid-tid with soft brush or cotton-tipped applicators for stomatitis; use unwaxed dental floss
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SIDE EFFECTS D CV: Increased B/P, sinus tachycardia, PVCs, chest pain, bradycardia, extrasys- toles, irreversible cardiomyopathy, acute left ventricular failure GI: Nausea, vomiting, anorexia, mucositis, hepatotoxicity GU: Impotence, sterility, amenorrhea, gynecomastia, hyperuricemia, urine discoloration HEMA: Thrombocytopenia, leukopenia, anemia RESP: Recall pneumonitis INTEG: Rash, necrosis at injection site, dermatitis, reversible alopecia, cel- lulitis, thrombophlebitis at injection site, radiation recall SYST: Anaphylaxis, secondary malignancy
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INTERACTIONS Increase: life-threatening dysrhythmias— posaconazole, fluconazole; do not use together Increase: QT prolongation—other drugs that increase QT prolongation Increase: neutropenia, thrombocytope- nia—progesterone Increase: cardiomyopathy—calcium- channel blockers Increase: toxicity—other antineoplas- tics, cycloSPORINE, radiation, mercapto- purine Increase: hemorrhagic cystitis risk, car- diac toxicity—cyclophosphamide Increase: effect of phenytoin, fosphenytoin Increase: DOXOrubicin effect—strepto- zocin Decrease: DOXOrubicin effect—PHENo- barbital Decrease: antibody response—live virus vaccine Decrease: clearance of DOXOrubicin— PACLitaxel Drug/Lab Test Increase: uric acid
Source pages 427, 428
Extracted information for DOXOrubicin only.
DOSAGE AND ROUTES • Adult: IV 60-75 mg/m2 every 3 wk, or 25-30 mg/m2 daily × 2-3 days, repeat q3-4wk or 20 mg/m2/wk, or may be used in combination with other antineoplas- tics with 40-75 mg/m2 every 21-28 days, max cumulative dose 550 mg/m2 or 450 mg/m2 if prior DAUNOrubicin, cyclo- phosphamide, mediastinal XRT • Child: IV 30 mg/m2/day × 3 days q4wk Hepatic dose • Adult: IV Bilirubin 1.2-3 mg/dL, give 50% of dose; bilirubin 3.1-5 mg/dL, give 25% of dose Renal dose • Adult: IV CCr <10 mL/min give 75% of dose
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Available forms: Powder for injection 10, 20, 50 mg/vial; solution for injec- tion 2 mg/mL
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Administer: IV route • Give antiemetic 30-60 min prior to product to prevent vomiting • Give allopurinol or sodium bicarbon- ate to maintain uric acid levels, alkalinza- tion of urine • Use cytotoxic handling procedures: inspect for particulate and discoloration prior to use
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Extracted information for DOXOrubicin only.
Assess:
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Evaluate: • Therapeutic response: decreased tu- mor size, spread of malignancy
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CLINICAL CONSIDERATIONS
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Patient and caregiver information: • To add 2-3 L of fluids unless contrain- dicated prior to and for 24-48 hr after to decrease possible hemorrhagic cystitis • To report any complaints, side effects to nurse or prescriber • That hair may be lost during treat- ment; that wig or hairpiece might make patient feel better; that new hair might be different in color, texture • That continuing follow-up and lab work will be needed • To notify health care professional of trouble breathing; swelling of hands, feet; increase in weight; change in heart rate • That body fluids should not be han- dled unless protective equipment is used • To discuss OTC, Rx, herbals, supple- ments with health care professional • To avoid foods with citric acid, hot temperature, or rough texture • To report any bleeding, white spots, ulcerations in mouth to prescriber; to examine mouth daily • That urine, other body fluids may be red-orange for 48 hr • To avoid crowds and persons with in- fections when granulocyte count is low • To avoid vaccinations • Pregnancy/breastfeeding: that bar- rier contraceptive measures are recom- mended during therapy and for 4 mo after ending therapy; to avoid breastfeeding HIGH ALERT
Source pages 428, 429
Extracted information for DOXOrubicin only.
PHARMACOKINETICS Half-life 30 min, terminal 16.5 hr; metabolized by liver; crosses placenta; excreted in urine, bile, breast milk
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Filter the extracted dose blocks for this individual drug.
• Adult: IV 60-75 mg/m2 every 3 wk, or 25-30 mg/m2 daily × 2-3 days, repeat q3-4wk or 20 mg/m2/wk, or may be used in combination with other antineoplas- tics with 40-75 mg/m2 every 21-28 days, max cumulative dose 550 mg/m2 or 450 mg/m2 if prior DAUNOrubicin, cyclo- phosphamide, mediastinal XRT
Candidate age grouping · source page 426
• Child: IV 30 mg/m2/day × 3 days q4wk Hepatic dose
Candidate age grouping · source page 426
• Adult: IV Bilirubin 1.2-3 mg/dL, give 50% of dose; bilirubin 3.1-5 mg/dL, give 25% of dose Renal dose
Candidate age grouping · source page 426
• Adult: IV CCr <10 mL/min give 75% of dose
Candidate age grouping · source page 426