Buy Leukeran
Leukeran

3.67
A chemotherapy medication used to treat specific types of blood and lymph system cancers.


Ingredient
Availability
In Stock
Delivery
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Alternative/Local Brand
Leukeran
Active Ingredient(s)
Chlorambucil
Primary Category
Cancer Treatment
Therapeutic Class
Antineoplastic agents, Alkylating agents, Nitrogen mustard analogues
Pharmacological Class
Nitrogen Mustards
Indications
Chronic lymphocytic leukaemia, Certain types of non-Hodgkin lymphoma, Hodgkin's disease, Waldenstrom's macroglobulinaemia
Contraindications
Pregnancy, Hypersensitivity to chlorambucil, Severe bone marrow suppression, Recent radiation therapy
Minor Side Effects
Nausea, Vomiting, Mouth sores
Moderate Side Effects
Skin rash, Lowered resistance to infections, Anaemia, Easy bruising
Serious Side Effects
Severe bone marrow suppression, Seizures, Infertility, Secondary malignancies, Lung fibrosis
Dosage Forms
Tablet
Administration Route
Oral
Mechanism of Action
Chlorambucil is an alkylating agent that works by attaching to and damaging the DNA of rapidly dividing cancer cells. This prevents the cells from replicating and carrying out normal functions, eventually leading to cell death and slowing the progression of the disease.
Prescription Status
Rx
Manufacturer
Aspen Pharma
Patient Summary
A chemotherapy medication used to treat specific types of blood and lymph system cancers.
Onset Time
Several weeks
Duration
Variable based on treatment cycle
Storage Instructions
Store in a refrigerator between 2°C and 8°C.
Drug Interactions
Live vaccines, Phenylbutazone, Other myelosuppressive drugs
Age Restrictions
Consult specialist for paediatric use
Pregnancy Use
Not recommended; can cause foetal harm. Effective contraception is required.
Alternative Drugs
Cyclophosphamide, Bendamustine, Fludarabine

What Is Leukeran?

Leukeran is a brand-name medication that contains the active ingredient chlorambucil. Chlorambucil belongs to a class of drugs known as alkylating agents and is used as an oncology support therapy. In Hong Kong, Leukeran is available only by prescription and is regulated by the Department of Health and the Pharmacy and Poisons Board. The medication is supplied as oral pill tablets in two strengths: 2 mg and 5 mg.

How Leukeran Works in the Body

Chlorambucil exerts its anticancer effect by attaching an alkyl group to DNA strands within rapidly dividing cells. This alkylation leads to cross-linking of DNA strands, which interferes with DNA replication and transcription. When cancer cells cannot properly duplicate their genetic material, they undergo programmed cell death (apoptosis).

Key pharmacologic features:

  • Onset of action: Clinical effects may become apparent within weeks of initiating therapy, as the drug gradually accumulates in target tissues.
  • Peak effect: Cytotoxic activity reaches its maximum after several treatment cycles, depending on dose and patient tolerance.
  • Duration: Chlorambucil has a relatively long half-life, allowing once-daily dosing.
  • Metabolism: The drug is metabolized primarily in the liver and excreted unchanged in the urine; renal function influences drug clearance.

Conditions Treated by Leukeran

Leukeran (chlorambucil) is approved in Hong Kong for the following indications:

  • Chronic lymphocytic leukemia (CLL) - to reduce the number of malignant lymphocytes and control disease progression.
  • Polycythemia vera (PV) - as a second-line option when first-line therapies are insufficient or not tolerated.
  • Certain low-grade non-Hodgkin lymphomas - when alternative agents are unsuitable.

These uses reflect regulatory approvals based on clinical trial data and expert consensus. The medication is generally prescribed for adult patients whose disease characteristics meet the criteria outlined in the product’s official label.

Evaluating Leukeran for Your Health Profile

Ideal Patient Characteristics

  • Adults with confirmed diagnoses of CLL, PV, or eligible low-grade lymphomas.
  • Individuals with adequate liver function (bilirubin ≤ 1.5 × upper limit of normal).
  • Patients whose bone-marrow reserve can tolerate potential myelosuppression.

Absolute Contraindications

  • Known hypersensitivity to chlorambucil or any component of the tablet.
  • Pregnant women (category D: associated with fetal toxicity).
  • Severe hepatic impairment (Child-Pugh C).
  • Uncontrolled infections or active severe cardiac disease.

Relative Contraindications

  • Moderate renal impairment (creatinine clearance < 30 mL/min) - dose reduction may be required.
  • Pre-existing bone-marrow suppression (e.g., low neutrophil or platelet counts).
  • Elderly patients (≥ 70 years) - may need closer monitoring.

Special Populations

  • Pregnancy & Lactation: Chlorambucil crosses the placenta and is excreted in breast milk; use is contraindicated.
  • Geriatric: Age-related decline in organ function may increase toxicity risk; start with the lower dose (2 mg) and titrate cautiously.

If any of the above conditions apply, a healthcare professional will determine whether Leukeran is appropriate or if alternative therapies should be considered.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Nausea or mild vomiting - often transient and may improve with food.
  • Transient leukopenia - a reduction in white blood cells that is usually reversible.
  • Mild fatigue - linked to bone-marrow suppression.
  • Hair thinning - typically mild and reversible after discontinuation.

Serious Adverse Events

  • Severe myelosuppression (neutropenia, thrombocytopenia) - may predispose to infections or bleeding; requires prompt medical evaluation.
  • Aplastic anemia - rare but life-threatening bone-marrow failure.
  • Secondary malignancies - long-term use carries a small risk of therapy-related cancers (e.g., myelodysplastic syndromes).

Patients should seek immediate medical attention for unexplained fever, easy bruising, persistent bleeding, or severe abdominal pain.

Drug Interactions

  • CYP2C9 inhibitors (e.g., fluconazole, amiodarone) - may increase chlorambucil plasma levels; dose adjustment may be necessary.
  • Other myelosuppressive agents (e.g., cyclophosphamide, methotrexate) - additive bone-marrow toxicity; close monitoring is essential.
  • Live vaccines - contraindicated while on chlorambucil due to impaired immune response.

If you are taking other prescription or over-the-counter medicines, inform your healthcare provider before starting Leukeran.

Food and Lifestyle Interactions

  • Food: Chlorambucil can be taken with or without food; consistent timing helps maintain stable blood levels.
  • Alcohol: Moderate consumption is generally acceptable, but excessive intake may worsen liver function and increase toxicity.
  • Driving: The medication rarely causes dizziness, but patients should assess their own alertness before operating machinery.

How to Take Leukeran

  • Standard dosing:
  • Initiate with 2 mg tablet once daily.
  • Depending on response and tolerability, the dose may be increased to 5 mg once daily.
  • Administration: Swallow the tablet whole with a glass of water. Do not crush, chew, or split the tablet unless directed by a pharmacist.
  • Timing: Take the dose at the same time each day to maintain steady drug levels.
  • Missed dose: If you forget a dose and it is less than 12 hours until the next scheduled dose, take the missed tablet. If it is longer than 12 hours, skip the missed dose and resume your regular schedule. Do not double the dose.
  • Overdose: Symptoms may include severe nausea, vomiting, diarrhea, and marked bone-marrow suppression. Seek emergency medical care; supportive care and hematopoietic growth factors are the mainstays of treatment.
  • Renal or hepatic impairment: Dose reductions are recommended; your prescriber will adjust the regimen based on laboratory results.
  • Treatment duration: Leukeran is usually prescribed for several months to years, depending on disease response. Never stop or alter the dose without professional guidance.

Monitoring and Follow-Up

  • Baseline labs: Complete blood count (CBC), liver function tests (LFTs), and renal function before initiating therapy.
  • Routine labs: CBC monitoring every 2-4 weeks during the first three months, then monthly if stable. LFTs and renal tests every 2-3 months.
  • Clinical assessment: Evaluate for signs of infection, bleeding, or new skin lesions at each visit.
  • Response evaluation: Hematologic parameters (e.g., lymphocyte count) and disease-specific markers are reviewed periodically to determine efficacy.

Regular follow-up with a hematology/oncology specialist is essential to balance therapeutic benefit against potential toxicity.

Storage and Handling

  • Store Leukeran tablets at room temperature (20 °C to 25 °C / 68 °F to 77 °F).
  • Keep the container tightly closed, away from moisture, heat, and direct sunlight.
  • Do not store in the bathroom or near a kitchen sink.
  • Keep out of reach of children and pets.
  • Dispose of unused tablets according to local pharmaceutical waste guidelines or return them to a pharmacy for safe disposal.

Medication-Specific Glossary

Alkylating Agent
A type of chemotherapy drug that adds alkyl groups to DNA, disrupting replication and leading to cell death.
Myelosuppression
Decreased production of blood cells by the bone marrow, resulting in lowered counts of white cells, red cells, or platelets.
Neutropenia
An abnormally low concentration of neutrophils, a key white-blood-cell type that fights infection.
Aplastic Anemia
A rare condition in which the bone marrow fails to produce sufficient new blood cells, potentially life-threatening.
Therapeutic Window
The dosage range in which a drug is effective without causing unacceptable toxicity.
Secondary Malignancy
A new cancer that arises as a delayed adverse effect of chemotherapy, distinct from the original disease.

Medical Disclaimer

This article provides educational information about Leukeran and is not a substitute for professional medical advice. Treatment decisions, including use for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Leukeran FAQ

Can I take Leukeran with other chemotherapy drugs?

Leukeran may be combined with other agents, but the risk of overlapping bone-marrow toxicity is higher. Your oncologist will assess the safety of any combination and adjust dosing or monitoring accordingly.

What should I do if I develop a fever while on Leukeran?

Fever can signal infection due to neutropenia. Contact your healthcare provider promptly; they may order blood tests and start antibiotics if an infection is suspected.

Is there a generic version of Leukeran available in Hong Kong?

Chlorambucil is available as a generic tablet in various strengths. Both brand-name and generic formulations contain the same active ingredient, but you should verify equivalence with your pharmacist.

How does food affect the absorption of chlorambucil?

Food does not significantly alter chlorambucil absorption. Taking the tablet with water, with or without meals, is acceptable; consistency helps maintain steady drug levels.

Can Leukeran cause hair loss?

Mild hair thinning may occur, but complete alopecia is uncommon with chlorambucil compared with some other chemotherapy agents. Hair loss is usually reversible after discontinuation.

Are there special considerations for travel with Leukeran?

Carry the medication in its original container, with a copy of the prescription. Verify that airport security permits the tablets, and keep them in your carry-on luggage to avoid temperature extremes.

What laboratory tests are required before each dose?

A complete blood count (CBC) is essential before each dose to ensure adequate white-cell and platelet counts. Liver and kidney function tests are performed periodically to guide dose adjustments.

Is Leukeran safe for patients with hepatitis B or C?

Patients with active hepatitis should be evaluated carefully, as liver impairment can increase drug toxicity. Your doctor may monitor liver enzymes more frequently or choose an alternative therapy.

How long does it take to see a clinical response in chronic lymphocytic leukemia?

Clinical improvement may be observed after several weeks to months of therapy, depending on disease burden and individual response. Ongoing monitoring helps determine treatment effectiveness.

Categories