Trade Names:BiCNU- Powder for injection 100 mg
Trade Names:Gliadel- Wafer 7.7 mg
Carmustine alkylates DNA and RNA and also inhibits several enzymes by carbamoylation of amino acids in proteins. Antineoplastic and toxic activities may be caused by metabolites.
Vd is 3.25 L/kg. Crosses the blood-brain barrier.
The t ½ is 22 min. Cl is 56 mL/min/kg. Approximately 60% is excreted in the urine; 6% is expired as CO 2 .
Brain tumors, multiple myeloma, Hodgkin and non-Hodgkin lymphomas; adjunct to surgery and radiation in newly diagnosed high-grade malignant glioma patients and as an adjunct in recurrent glioblastoma multiforme patients (wafer).
IV 150 to 200 mg/m 2 every 6 wk, as a single dose or divided into 2 successive daily infusions.Dosage ReductionAdults
IV Compromised bone marrow function or therapy with other myelosuppressive drugs requires a reduction in dose. Do not administer repeat courses until acceptable leukocyte and platelet counts have recovered (usually greater than 4,000/mm 3 and 100,000/mm 3 , respectively). Subsequent doses are determined by the clinical and hematologic tolerance of the previous dose. The following leukocyte and platelet counts refer to the levels reached at nadir after prior dose. Give 100% of the prior dose given if the leukocytes are greater than 3000 cells/mm 3 and the platelets are greater than 75,000 cells/mm 3 . Give 70% of the prior dose given if the leukocytes are 2000 to 2999 cells/mm 3 and the platelets are 25,000 to 74,999 cells/mm 3 . Give 50% of the prior dose given if the leukocytes are less than 2000 cells/mm 3 and the platelets are less than 25,000 cells/mm 3 .Adjunct To Surgery And Radiation In Newly Diagnosed High-Grade Malignant Glioma Patients And As An Adjunct In Recurrent Glioblastoma Multiforme PatientsAdults
Wafer for implantation 8 wafers placed in the resection cavity, for a total dose of 61.6 mg. If the cavity size and shape will not accommodate this, use the greatest number of wafers that will fit.
Store the unopened vials in a refrigerator (2° to 8°C; 3° to 46°F). After reconstitution, store at room temperature (25°C; 77°F) for up to 8 h. Protect from light.Wafer
Store at or below –20°C (–4°F). Unopened foil pouches may be kept at room temperature for up to 6 h.
Cimetidine may enhance the myelosuppressive effects of carmustine.Digoxin, phenytoin
Digoxin and phenytoin serum levels may be reduced by carmustine.
None well documented.
Deep thrombophlebitis (10%); pulmonary embolus (8%); hemorrhage (7%).
Depression (16%); intracranial hypertension (9%); anxiety, facial paralysis (7%); ataxia, hypesthesia (6%); dizziness, hallucinations, seizures (5%); headache (28%); meningitis; abscess; asthenia; confusion; somnolence; brain edema; intracranial infection.
Rash (wafer) (12%); local burning pain at the injection site; intense flushing of the skin.
Constipation (19%); abdominal pain, diarrhea (5%), (wafer); nausea (22%); vomiting (21%).
UTI (8%; wafer); amenorrhea; male infertility.
Bone marrow suppression; myelosuppression.
Transient LFT elevations; hepatic necrosis and veno-occlusive disease after bone marrow transplantation.
Diabetes mellitus (wafer).
Dose-related, delayed-onset, progressive renal failure.
Early pulmonary toxicity; delayed pulmonary fibrosis.
Retinitis; optic neuritis; suffusion of the conjunctiva.
Surgical wound healing abnormalities (16%); fever (12%); back pain, pain (7%); face edema (6%); abscess, chest pain (5%); CSF leak; subdural fluid collection; subgaleal or wound effusion; wound breakdown.
WarningsBone marrow suppression (notably thrombocytopenia and leukopenia)
May contribute to bleeding and infections. Toxicity is cumulative, thus adjust dose based on nadir counts from prior doses. Do not repeat doses more frequently than every 6 wk. Perform weekly complete blood cell counts for 6 wk postdose.Hematologic
The most frequent and serious toxic effect of injectable carmustine is delayed myelosuppression.Pulmonary fibrosis
Delayed onset pulmonary fibrosis has occurred up to 17 yr after treatment and has been reported in patients who received injectable carmustine in childhood and early adolescence.Pulmonary toxicity
Pulmonary toxicity from injectable carmustine appears to be dose-related. Patients receiving more than 1400 mg/m 2 cumulative dose are at significantly higher risk than those receiving less. Other risk factors include history of lung disease and duration of treatment. Cases of fatal pulmonary toxicity have occurred.
MonitorLiver/Renal function tests
Monitor liver and renal function tests periodically.Pulmonary function tests
Conduct baseline pulmonary function studies and frequent pulmonary function tests during treatment. Patients with a baseline less than 70% of predicted forced vital capacity (FVC) or carbon monoxide diffusing capacity (DL co ) are at particular risk.
Category D .
Safety and efficacy not established.
Long-term use of nitrosoureas has been reported to be associated with the development of secondary malignancies.
There have been reports of persistent testicular damage causing infertility with injectable carmustine.
Brain edema was noted in 4% of patients treated with the wafer.
Cases of intracerebral mass effect unresponsive to corticosteroids have been described in patients treated with the wafer.
Nausea and vomiting after IV administration. This dose-related toxicity appears within 2 h of dosing and lasts 4 to 6 h.
The majority of these events were mild to moderate in severity.
Reversible hepatic toxicity, manifested by increased transaminase, alkaline phosphatase, and bilirubin levels, has occurred in a small percentage of patients using injectable carmustine.
Intracranial infection (eg, meningitis, abscess) occurred in 4% to 5% of patients treated with the wafer.
Avoid communication between the surgical resection cavity and the ventricular system to prevent the wafers from migrating into the ventricular system and causing obstructive hydrocephalus.
Toxicity manifested as nerve fiber-layer infarcts and retinal hemorrhages has been associated with high dose injectable carmustine therapy.
Decrease in kidney size, progressive azotemia, and renal failure have occurred in patients.
The majority of seizures in the placebo vs wafer study were mild or moderate in severity.
Remnants of implanted wafers may be observed on brain imaging scans or during later operations even though all components are extensively degraded. Remnants removed from 2 patients after 64 and 92 days contained less than 0.0004% and 0.034%, respectively, of the original carmustine content. Remnants may persist for up to 232 days after implantation.
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