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Capecitabine adverse effects

Ixabepilone, a microtubule stabilizing agent, is indicated as monotherapy or in combination with capecitabine in MBC patients who have previously received an anthracycline and a taxane. Response rates and time to progression were increased with combination therapy as compared with capecitabine alone. Adverse effects include myelosuppression, peripheral neuropathy, and myalgias/arthralgias. [Pg.700]

Although not a taxane, ixabepilone is a novel microtubule inhibitor that was recently approved for metastatic breast cancer in combination with the oral fluoropyrimidine capecitabine or as monotherapy. It is a semisynthetic analog of epothilone B, and is active in the M phase of the cell cycle. This agent binds directly to 6-tubulin subunits on microtubules, leading to inhibition of normal microtubule dynamics. Of note, this agent continues to have activity in drug-resistant tumors that overexpress P-glycoprotein or tubulin mutations. The main adverse effects include myelosuppression, hypersensitivity reactions, and neurotoxicity in the form of peripheral sensory neuropathy. [Pg.1177]

Generic Name Capecitabine Trade Name Xeloda Primary Antineoplastic lndication(s) Breast cancer Common Adverse Effects Blood disorders [anemia, neutropenia, thrombocytopenia] Gl distress [abdominal pain, nausea, vomiting] dermatitis stomatitis unusual tiredness... [Pg.571]

Her estimated creatinine clearance is 74 mL/min. This represents a relatively normal renal function, particularly for someone of Mrs RP s age. The Summary of Product Characteristics for capecitabine (Summary of Product Characteristics, 2008) states that the dosage only needs to be reduced if creatinine clearance is between 30 and 50 mL/min, to 75% dosage. If creatinine clearance is <30 mL/min, then capecitabine is contraindicated. This is because the incidence of severe adverse effects is more common in patients with renal impairment compared with the overall population. [Pg.213]

It is imperative for patients to manage the side-effects of oral chemotherapy appropriately. This includes knowing when to stop taking the tablets should severe adverse effects occur. There are clear recommendations for stopping capecitabine should certain specific side-effects occur whilst taking the drug and contacting the treatment centre for further advice. These include ... [Pg.216]


See other pages where Capecitabine adverse effects is mentioned: [Pg.1392]    [Pg.202]    [Pg.453]    [Pg.202]    [Pg.475]    [Pg.280]    [Pg.633]    [Pg.1353]    [Pg.2356]   
See also in sourсe #XX -- [ Pg.1284 , Pg.1313 , Pg.1350 , Pg.1350 ]

See also in sourсe #XX -- [ Pg.183 , Pg.210 ]

See also in sourсe #XX -- [ Pg.2297 , Pg.2356 ]




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Capecitabin

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