Cetuximab is a monoclonal antibody that specifically targets the extracellular ligand-binding domain of the Epidermal Growth Factor Receptor (EGFR). By binding to EGFR, it competitively blocks the attachment of natural ligands, thereby inhibiting downstream signaling pathways crucial for cell growth, proliferation, and survival. This action leads to reduced tumor growth in EGFR-expressing cancers.
Treatment of wild-type RAS metastatic colorectal cancer in patients with tumours expressing epidermal growth factor receptor, as combination therapy, or as monotherapy if oxaliplatin- and irinotecan-based therapy has failed or if irinotecan is not toleratedTreatment of locally advanced squamous cell cancer of the head and neckcolorectal cancer (KRAS wild type)metastatic colorectal cancer with wild-type KRAS in combination with chemotherapyhead and neck squamous cell carcinoma (HNSCC) in combination with radiation or cisplatinmonotherapy for patients with metastatic or recurrent HNSCC whose disease progresses on platinum-based chemotherapyAdvanced/metastatic squamous carcinoma of head and neckEGF receptor positive metastatic colorectal cancer
- Adult
- with paclitaxel for the treatment of adult patients with platinum-resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other vascular endothelial growth factor (VEGF) inhibitors or VEGF receptor-targeted agents.…
Common
acneiform rashpruritusnail changesheadachediarrheaAcneform skin rashItchingDiarrhoea
Serious
- Necrotising fasciitis
- Congestive heart failure
- Posterior reversible encephalopathy syndrome
- Seizures
- Headache
- Altered mental status
- Visual disturbance
- Cortical blindness
- Osteonecrosis of jaw
- Hypertension
- infusion reactions
- cardiopulmonary arrest (in HNSCC patients receiving radiation or chemotherapy)
- interstitial lung disease
- serum electrolyte imbalances (hypomagnesemia)
- Anaphylactoid reactions
- Hypomagnesemia
Avoid—toxicity in animal studies.
Manufacturer advises avoid breastfeeding during and for at least 6 months after treatment.
Aminolevulinic AcidSevere
Database
Clinical effect not specified
Source: DDInter
ThalidomideSevere
Database
Drug interaction classified as: synergy
Source: DDInter
10 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.