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Vilban is consists of Vinblastine, is a chemotherapy medication derived from the periwinkle plant (Catharanthus roseus). It belongs to the vinca alkaloid class of drugs and is primarily used for treating various cancers, including Hodgkin’s lymphoma, non-Hodgkin’s lymphoma, breast cancer, testicular cancer, and Kaposi’s sarcoma. Vinblastine works by inhibiting microtubule formation, preventing cancer cells from dividing and proliferating. Vinblastine remains a cornerstone in cancer chemotherapy, particularly for Hodgkin’s lymphoma, testicular cancer, and Kaposi’s sarcoma. Its role in combination regimens has significantly improved survival rates for many patients. However, its myelosuppressive effects necessitate careful monitoring. With ongoing advancements in drug delivery and combination therapies, vinblastine’s effectiveness may continue to improve in the coming years.
Vinblastine is a mitotic inhibitor that functions by binding to tubulin, a protein essential for microtubule formation. Microtubules play a crucial role in cell division, and by preventing their assembly, vinblastine halts mitosis in the metaphase, leading to cancer cell death.
Microtubule Disruption: Prevents mitotic spindle formation, blocking cell division.
Apoptosis Induction: Leads to programmed cell death in rapidly dividing cancer cells.
Reduced Angiogenesis: Inhibits the formation of new blood vessels that feed tumors.
Hodgkin’s Lymphoma – Used in combination chemotherapy regimens like ABVD (Adriamycin, Bleomycin, Vinblastine, and Dacarbazine).
Non-Hodgkin’s Lymphoma – Effective in slowing disease progression.
Testicular Cancer – Part of BEP (Bleomycin, Etoposide, and Platinum-based therapy).
Breast Cancer – Used in advanced-stage or recurrent cases.
Kaposi’s Sarcoma – Treats aggressive cases in immunocompromised patients (e.g., HIV/AIDS-related Kaposi’s sarcoma).
Bladder Cancer & Lung Cancer – Investigated for efficacy in metastatic settings.
Typical Dosages:
Lymphomas: 6 mg/m² IV every 7-14 days.
Testicular Cancer: 3 mg/m² IV weekly.
Breast Cancer & Kaposi’s Sarcoma: Dosage varies depending on combination regimens.
Pediatric Dosing: Adjusted based on body surface area (BSA) and tolerance.
Hodgkin’s Lymphoma (ABVD Trial):
Improved survival rates with ABVD vs. older regimens.
High complete remission rates (~80%).
Testicular Cancer (BEP Regimen Studies):
High cure rates (~90%) in early-stage disease.
Kaposi’s Sarcoma (AIDS-Related Trials):
Effective in reducing tumor burden.
Common Side Effects:
Bone Marrow Suppression: Leads to leukopenia (low white blood cell count), increasing infection risk.
Gastrointestinal Issues: Nausea, vomiting, constipation.
Neuropathy: Mild to moderate peripheral neuropathy.
Alopecia: Temporary hair loss.
Fatigue & Weakness.
Serious Side Effects:
Severe Myelosuppression: Can lead to life-threatening infections.
Neurotoxicity: Less common than vincristine but can still occur.
Extravasation Risk: Severe local tissue necrosis if it leaks outside the vein.
Contraindications:
Severe leukopenia (low WBC count).
Hypersensitivity to vinca alkaloids.
Pregnancy and breastfeeding.
Precautions:
Renal & Hepatic Impairment: Dose adjustments required.
Neuropathy Risk: Monitor for tingling or numbness.
Vaccinations: Avoid live vaccines during therapy.
CYP3A4 Inhibitors (e.g., Ketoconazole, Erythromycin): Increase vinblastine levels, enhancing toxicity.
CYP3A4 Inducers (e.g., Rifampin, Carbamazepine): Reduce vinblastine efficacy.
Other Chemotherapy Agents: Increased bone marrow suppression when combined with cisplatin or doxorubicin.
Antifungal Medications (Itraconazole, Fluconazole): May exacerbate side effects.
Store at 2-8°C (Refrigerated).
Protect from light to prevent degradation.
Use within prescribed time after dilution.
Safe disposal required due to cytotoxic nature.
Vilban is used to treat the following -
Main Benefits
Other Benefits
This is the usual dosage recommended in most common treatment cases. Please remember that every patient and their case is different, so the dosage can be different based on the disease, route of administration, patient's age and medical history.
Find the right dosage based on disease and age
Age Group | Dosage |
Adult(Female) |
|
Geriatric |
|
Adult |
|
Adult(Male) |
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13 - 18 years (Adolescent) |
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Is the use of Vilban safe for pregnant women?
Pregnant women may get severe side effects after taking Vilban. If you are pregnant, do not take Vilban without a doctor's advice.
Is the use of Vilban safe during breastfeeding?
Vilban may cause serious side effects in breastfeeding women, so do not take this drug without doctor's advice.
What is the effect of Vilban on the Kidneys?
Vilban is not harmful for kidneys.
What is the effect of Vilban on the Liver?
There may be an adverse effect on the liver after taking Vilban. If you observe any side effects on your body then stop taking this drug. Take this medicine again only if your doctor advises you to do so.
What is the effect of Vilban on the Heart?
You can take Vilban without any fear of damage to the heart.
Vilban should not be taken with following medicines due to severe side effects it may cause to patients -
Severe
If you are suffering from any of the following diseases, you should not take Vilban unless your doctor advises you to do so -
Is this Vilban habit forming or addictive?
Vilban is not addictive in nature.
Is it safe to drive or operate heavy machinery when consuming?
No, you should do not do anything that requires concentration and attention as the Vilban can make you feel drowsy.
Is it safe?
Vilban is safe but it is important to consult a doctor before taking it.
Is it able to treat mental disorders?
There is no benefit of taking Vilban for mental disorders.
Interaction between Food and Vilban
Taking Vilban with food does not cause any problems.
Interaction between Alcohol and Vilban
Due to lack of research, nothing can be said about side effects of consuming alcohol while taking Vilban.
This medicine data has been created by -
B.Pharma, Pharmacy
5 Years of Experience
References
KD Tripathi. [link]. Seventh Edition. New Delhi, India: Jaypee Brothers Medical Publishers; 2013: Page No 865