Alexan, 50 mg/ml ml

Antitumor drug. It belongs to the group of pyrimidine metabolites and is an S-phase-specific drug. It inhibits DNA synthesis. As a result of phosphorylation it is converted into arabinosyl cytosine triphosphate (Ara-CTP), which competitively inhibits DNA polymerase. In addition, there is evidence that DNA synthesis is also inhibited by the incorporation of cytarabine into the DNA and RNA molecule.

Possible development of resistance to cytarabine is associated with inhibition of membrane transport, deficiency of phosphorylating enzymes, increased inactivating enzyme activity, decreased DNA polymerase affinity or increased deoxy-CTPase pool. Cytotoxic action is achieved by creating constant high intracellular concentrations of Ara-CTF.

Indications

High-dose cytarabine therapy:

Active ingredient

Composition

1 ml of 50 mg/ml solution contains::

Active ingredients: cytarabine 50.00 mg;

Additional ingredients: sodium lactate 60 % solution 10.40 mg, lactic acid (pH regulator) 0.045 mg, water for injection up to 1 ml.

How to take, the dosage

The regimen and method of administration varies with different chemotherapy regimens.

The use of Alexan® is only possible in specialized clinics under medical supervision. Alexan® is not active when administered orally.

The Alexan® drug may be used both in monotherapy and in combination with cytostatics and, in some cases, glucocorticosteroids.

The drug Alexan® may be administered intravenously (bolus or drip), subcutaneously, intramuscularly (usually used only for maintenance of remission therapy), and intrathecally.

The average daily dose is 100-200 mg/m2. For elderly patients or those with decreased hematopoietic reserves, the daily dose should not exceed 50-70 mg/m2.

Induction of remission in acute leukemia: in combination with other antitumor drugs – 100 mg/m2/day as a continuous rapid or slow intravenous infusion for 5-10 days or intravenously every 12 hours for 7 consecutive days. A total of 4-7 treatment courses are carried out. The intervals between courses are at least 14 days.

High-dose therapy: high-dose therapy in treatment of leukemia with poor prognosis, as well as of refractory leukemia and relapses is carried out with the use of Aleksan® at a dose of 2-3 g/m2 of body surface in the form of intravenous infusion lasting 1-3 hours, with 12-hour intervals, for 4-6 days as monotherapy or in combination with other antitumor drugs.

Intrathecal therapy (treatment of leukemic lesions of the central nervous system): In acute leukemia the dose of Alexan® is 5-75 mg/m2. The frequency of administration may vary from once a day for 4 days to once every 4 days. Most commonly, cytarabine is administered at 30 mg/m2 of body surface every 4 days until normalization of parameters, followed by another additional administration. However, the dose and intervals between injections depend on the clinical situation. Due to the fact that the dosage and regimen of Alexan® depend on tailored polychemotherapy regimens, specific literature should be consulted in each individual case.

In cases of renal and hepatic impairment, Alexan® should be used with caution and the dose should be reduced if necessary, especially in patients with significant hepatic and renal impairment.

Citarabine is excreted by hemodialysis. It is not recommended to use the drug immediately before and immediately after a dialysis session.

In elderly patients (over 60 years of age), high-dose therapy may be used only after careful assessment of the benefit/risk ratio.

Preparation of solution for infusion

The Alexan® drug in the required dose is diluted in 0.9% sodium chloride solution or in 5% dextrose solution. The concentration of cytarabine should not exceed 100 mg/ml.

In intrathecal administration of Alexan®, 0.9% sodium chloride solution or 5% dextrose solution may be used. Solvents containing preservatives should not be used.

It is recommended that 5-8 ml of cerebrospinal fluid be taken first, mixed with the solution for injection in the syringe, and then the resulting solution should be slowly injected back.

The solution should be drawn from the bottle immediately prior to use.

Please only use freshly prepared clear solutions and only once!

Interaction

Special Instructions

The use of the drug Aleksan® should be carried out under the supervision of a qualified physician experienced in working with antitumor chemotherapy drugs and only under hospital conditions. Aleksan® can be used both as monotherapy and in combination with other antitumor drugs. The dose and regimen of the drug are chosen individually. In case of combined therapy it is necessary to take into account cumulative myelosuppressive effect of all drugs included into the scheme of treatment.

When working with the drug Alexan® care must be taken. The drug should be diluted under aseptic conditions in a specially designated room. This should be done by trained personnel. All measures should be taken to prevent contact of the cytarabine solution with skin and mucous membranes, in particular, protective clothing (gown, cap, mask, glasses and disposable gloves) should be worn. If citarabine comes into contact with the skin or mucous membranes, you should wash thoroughly with soap and water or (eyes) with plenty of water. Cytarabine strongly suppresses bone marrow function. Therapy with Alexan® should be started with caution in patients with pre-existing myelosuppression. Clinical blood count (daily during induction therapy), uric acid concentration in plasma, function of bone marrow, liver, kidneys, central nervous system, lungs should be controlled regularly. If platelets fall below 50000/mm3 or polymorphonuclear granulocytes fall below 1000/mm3, the treatment regimen should be suspended or changed. Peripheral blood platelet counts may continue to fall after drug withdrawal and reach a minimum level after 12-24 days. If indicated, therapy may be resumed when there are clear signs of hematopoiesis recovery based on the results of bone marrow examination.

We should keep in mind that complications such as bleeding (secondary to thrombocytopenia) and severe infection (secondary to granulocytopenia) may develop.

There have been reports of severe CNS, gastrointestinal and pulmonary toxicity (different from that of standard cytarabine therapy), sometimes with lethal outcome. Reversible damage of the cornea of the eye is possible; impairment of brain function, especially of the cerebellum, which are usually reversible, drowsiness, convulsions; severe gastrointestinal ulcers, including cystic pneumatosis of the intestine, which may lead to peritonitis; sepsis, liver abscess, pulmonary edema.

The occurrence of peripheral motor and sensory neuropathy has been reported after coadministration of high doses of cytarabine, daunorubicin, and asparaginase in adult patients with acute non lymphoblastic leukemia. Therefore, caution should be exercised when using high-dose cytarabine and timely dose adjustments should be made to avoid irreversible neurological disorders. There have been reports of delayed progressive ascending paralysis resulting in death in children with acute myeloleukemia after intrathecal and intravenous administration of cytarabine in usual doses in combination with other drugs.

In patients who have previously received treatment with CNS-damaging effects, such as intrathecal chemotherapy or radiation therapy, the risk of neurotoxicity increases with high doses of cytarabine. When cytarabine is administered rapidly intravenously, nausea and vomiting often occur within hours of administration. It is possible to reduce the incidence and severity of these side effects when using the drug by infusion. The literature describes cases of peritonitis and colitis with a positive test for occult blood in combination with neutropenia and thrombocytopenia in patients when using conventional doses of cytarabine in combination with other drugs. Patients have been successfully treated without surgery. There are reports of the occurrence of cardiomyopathy (including fatal) when using high-dose cytarabine in combination with cyclophosphamide. In case of cytarabine syndrome the use of Aleksan® should be stopped and treatment with glucocorticosteroids should be started. If steroid therapy is effective, treatment with cytarabine may be continued.

In order to prevent hemorrhagic conjunctivitis, local use of glucocorticosteroids is recommended.

Caution should be exercised when using the drug in patients with impaired hepatic and renal function.

High-dose therapy and intrathecal therapy should not use solutions containing benzyl alcohol.

As with other anticancer agents, the drug Alexan® may cause hyperuricemia due to rapid decay of tumor cells. Prevention of hyperuricemia is recommended in patients with a high blast cell count or large tumor masses (for example, in non-Hodgkin’s lymphoma): provide allopurinol and adequate fluid intake.

Inoculation of patients receiving therapy with Alexan® should be performed with extreme caution, after careful evaluation of hematologic status and with the consent of the physician administering the cytarabine therapy. The interval between the end of immunosuppressive therapy and vaccination depends on the type of immunosuppressant, underlying disease, and other factors and varies from 3 months to 1 year. Cytarabine is eliminated from the body by hemodialysis. Therefore, patients on dialysis should not be given Alexan® immediately before and during dialysis.

Women and men as well as their sexual partners should use reliable contraception during treatment and for 6 months after completion.

Impact on driving and operating machinery

Patients receiving chemotherapy may have impaired ability to drive and operate machinery, so if possible, they should refrain from engaging in potentially dangerous activities that require increased concentration and quick psychomotor reactions.

Contraindications

Side effects

Overdose

Symptoms: vomiting, diarrhea, marked suppression of bone marrow function, bleeding, development of infection, symptoms of neurotoxicity (impaired consciousness, motor disorders, seizures, cognitive disorders).

Treatment: there is no specific antidote. If an overdose occurred, symptomatic therapy (hemotransfusion) should be carried out. In case of severe overdose, after intrathecal administration, spinal fluid should be immediately replaced with isotonic saline solution. Cytarabine is excreted by hemodialysis. However, there is no information on the effectiveness of hemodialysis for cytarabine overdose.

Pregnancy use