Sotoxen contains Sotorasib, a selective KRAS G12C inhibitor indicated for adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) harboring the KRAS G12C mutation, who have received at least one prior systemic therapy. Sotorasib selectively targets KRASG12C, an oncogenic driver in many cancers, inhibiting tumor cell signaling, growth, and promoting apoptosis.
By covalently binding the unique cysteine in KRASG12C, Sotorasib locks the protein in an inactive state, blocking downstream oncogenic pathways without affecting wild-type KRAS, ensuring selective anti-tumor activity. Preclinical studies have shown Sotorasib also promotes anti-tumor immune responses in KRASG12C-expressing tumors.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
KRAS G12C-mutated NSCLC (locally advanced or metastatic)
Patients who have received at least one prior systemic therapy
Therapy guided by an FDA-approved KRAS G12C test
Mechanism of Action: Covalent, irreversible inhibition of KRAS G12C
Effect: Blocks tumor cell signaling, inhibits growth, induces apoptosis
Selectivity: Minimal off-target activity; locks KRASG12C in inactive state
Additional Effects: Enhances antigen presentation and inflammatory cytokine production selectively in KRASG12C tumor cells
Recommended Dose: 960 mg orally once daily (eight 120 mg tablets)
Administration: With or without food; swallow tablets whole
Missed Dose: If >6 hours late, take next dose at usual time; do not double dose
Vomiting: Do not take an additional dose; continue next day as scheduled
Treatment Duration: Continue until disease progression or unacceptable toxicity
Acid-reducing agents: Avoid PPIs, H2 blockers, and antacids if possible; if necessary, adjust timing
CYP3A4 inducers: Avoid strong inducers (e.g., rifampicin, carbamazepine)
CYP3A4 substrates: Avoid co-administration with sensitive substrates; may require dose adjustment
P-gp substrates: Caution with digoxin and other P-gp substrates; monitor for toxicity
Hepatotoxicity: Liver dysfunction including elevated AST, ALT, bilirubin, or drug-induced hepatitis
Interstitial Lung Disease (ILD)/Pneumonitis: Rare but potentially fatal; monitor for respiratory symptoms
Monitoring: Regular liver function tests every 3 weeks for first 3 months, then monthly
Hepatotoxicity: May require dose interruption, reduction, or permanent discontinuation
ILD/Pneumonitis: Immediately withhold if suspected; permanently discontinue if no alternative cause found
Patient Monitoring: Liver function, respiratory symptoms, and overall tolerance
Other Risks: Reproductive toxicity in animal studies; unknown effects in pregnancy and lactation
Pregnancy: No human data; animal studies show reproductive toxicity
Breastfeeding: Unknown if excreted in human milk; weigh benefits of therapy vs. breastfeeding
No clinical experience with overdose
Management: Symptomatic and supportive care as needed
Cytotoxic Chemotherapy / KRAS G12C Inhibitor
Store below 25°C in a cool, dry place, protected from light
Keep out of reach of children
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