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ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › ANTINEOPLASTIC AGENTS › PLANT ALKALOIDS AND OTHER NATURAL PRODUCTS › Taxanes
paclitaxel and encequidar
L01CD51
Forms & Strengths
- Oral tablet: paclitaxel 20 mg combined with encequidar 15 mg
Adult Dosing
- Metastatic breast cancer: 205 mg paclitaxel / 15 mg encequidar orally once daily on Days 1, 8, and 15 of a 28-day cycle
- Administer on an empty stomach (fast for 4 hours before and 2 hours after administration)
- Premedicate with an antiemetic as appropriate
Pediatric Dosing
- Safety and efficacy in pediatric patients have not been established
Indications
- Treatment of metastatic breast cancer
Mechanism of Action
- Paclitaxel is a taxane that stabilizes microtubules, inhibits depolymerization, and arrests cell division
- Encequidar is a potent P-glycoprotein inhibitor co-administered to enhance the intestinal absorption and oral bioavailability of paclitaxel
Contraindications
- Baseline neutrophil count < 1,500 cells/mm3
- Severe hepatic impairment
- Known hypersensitivity to paclitaxel, encequidar, or Cremophor EL (if applicable formulation context)
Adverse Reactions
- Neutropenia, leukopenia, anemia, thrombocytopenia
- Peripheral neuropathy
- Nausea, vomiting, diarrhea, abdominal pain
- Fatigue, asthenia
- Alopecia
- Musculoskeletal pain, arthralgia, myalgia
Drug Interactions
- Avoid strong CYP2C8 and CYP3A4 inhibitors and inducers, as paclitaxel is metabolized by these enzymes
- Avoid strong P-glycoprotein inhibitors or inducers that may unpredictably alter encequidar or paclitaxel absorption
- Use caution with medications known to prolong the QT interval or cause myelosuppression
Curated Content: Needs Vetting Before Put to Clinical Use