Caboxen 80 mg, containing the active ingredient Cabozantinib, is an advanced tyrosine kinase inhibitor (TKI) designed for the treatment of various cancers, including advanced renal cell carcinoma (RCC) and hepatocellular carcinoma (HCC). As a multi-kinase inhibitor, Caboxen targets several critical pathways involved in tumor growth, angiogenesis, and metastasis, including VEGFRs, MET, and AXL. Manufactured under stringent pharmaceutical standards, Caboxen represents a significant innovation in oncology therapeutics, providing a targeted treatment option for patients with advanced cancers.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Targeted Cancer Therapy / Tyrosine Kinase Inhibitor
Caboxen 80 mg is indicated for:
Advanced renal cell carcinoma (RCC) in adults who have received prior anti-angiogenic therapy
Hepatocellular carcinoma (HCC) in adults who have previously been treated with sorafenib
Caboxen may also be used for other cancers under clinical supervision or in ongoing trials, as guided by oncologists.
Cabozantinib is a multi-targeted TKI that inhibits key kinases involved in tumor proliferation and angiogenesis:
VEGFR1-3: Prevents formation of new blood vessels that supply tumors
MET and AXL: Reduces tumor growth, metastasis, and resistance to therapy
By inhibiting these pathways, Cabozantinib slows tumor progression, reduces metastasis, and can improve survival outcomes in patients with RCC and HCC.
Pharmacokinetics:
Absorption: Peak plasma concentration occurs 2–5 hours after oral administration
Metabolism: Primarily via CYP3A4, with caution required when co-administered with CYP3A4 modulators
Half-life: Approximately 99 hours, supporting once-daily dosing
Recommended dose: 80 mg orally, once daily, with or without food
Tablets should be swallowed whole; do not crush or chew
Continue treatment until disease progression or unacceptable toxicity occurs
Missed dose: Take the next dose at the scheduled time; do not double the dose to compensate
Dose adjustments may be required for adverse reactions such as hypertension, hand-foot syndrome, diarrhea, or elevated liver enzymes
CYP3A4 inhibitors (e.g., ketoconazole) may increase Cabozantinib exposure; monitor for toxicity
CYP3A4 inducers (e.g., rifampicin) may reduce efficacy
Avoid co-administration with drugs that prolong QT interval or have narrow therapeutic windows without monitoring
Common adverse effects include:
Gastrointestinal: Diarrhea, nausea, vomiting
Dermatologic: Hand-foot syndrome, rash
Cardiovascular: Hypertension
Hematologic: Fatigue, anemia, thrombocytopenia
Hepatic: Elevated liver enzymes
Serious but less frequent side effects include hemorrhage, gastrointestinal perforation, and cardiac events, requiring close monitoring.
Cabozantinib may cause fetal harm; not recommended during pregnancy
Effective contraception is required during treatment and for 4 months after the last dose
Breastfeeding should be avoided during treatment and for a defined washout period
Monitor blood pressure, liver function, and electrolytes regularly
Interrupt or reduce dosage for severe toxicities such as GI perforation, hemorrhage, or severe hypertension
Patients should be counseled on sun protection due to photosensitivity risks
No dose adjustment required for mild to moderate renal or hepatic impairment
Safety in pediatric patients is not established
Limited data for elderly patients, though tolerability is generally consistent with younger adults
Store below 30°C, in a dry and dark place
Keep out of reach of children
Protect tablets from moisture and light.
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