Informational only — Not medical advice. Always consult a licensed healthcare provider.

Community data Updated 2 months ago

Indications

Ovarian Carcinoma: Paxel is indicated as first-line and subsequent therapy for the treatment of advanced carcinoma of the ovary. As first-line therapy, Paxel is indicated in combination with cisplatin. Breast Carcinoma: Paxel is indicated for the adjuvant treatment of node-positive breast cancer, given sequentially after standard doxorubicin-containing combination chemotherapy. Paxel is indicated for the treatment of breast cancer after failure of combination chemotherapy for metastatic disease, or relapse within 6 months of adjuvant chemotherapy. Prior therapy should have included an anthracycline unless clinically contraindicated. Paxel is indicated for the first-line therapy of advanced or metastatic breast cancer, either in combination with an anthracycline in patients for whom anthracycline therapy is suitable, or in combination with trastuzumab in patients whose tumours overexpress HER2 at a 2+ or 3+ level as determined by immunohistochemistry. Gemcitabine, in combination with Paxel, is indicated in the treatment of patients with unresectable, locally recurrent or metastatic breast cancer who have relapsed following adjuvant or neoadjuvant chemotherapy. Prior chemotherapy should have included an anthracycline unless clinically contraindicated. Paxel is indicated for the treatment of metastatic cancer of the breast, in combination with trastuzumab, in patients who have tumours that overexpress HER2 and who have not received previous chemotherapy for their metastatic disease. Non-Small Cell Lung Carcinoma: Paxel, in combination with cisplatin, is indicated for the first-line treatment of non-small cell lung cancer in patients who are not candidates for potentially curative surgery and/or radiation therapy. Kaposi's Sarcoma: Paxel is indicated for the second-line treatment of AIDS-related Kaposi's sarcoma. Gastric Carcinoma: Paxel is indicated for the treatment of gastric carcinoma.

⚠️ Always consult a registered physician before taking any medicine.

Pharmacology

Paclitaxel is a novel anti-microtubule agent. It promotes the assembly of microtubules from tubulin dimers and stabilizes microtubules by preventing depolymerization. This stability blocks the normal dynamic reorganization of the microtubule network, a process the cell depends on for vital interphase and mitotic functions. Paclitaxel also induces abnormal arrays or "bundles" of microtubules throughout the cell cycle, along with multiple asters of microtubules during mitosis. After intravenous administration, plasma concentrations of paclitaxel decline in a biphasic manner. The initial rapid decline reflects distribution into the peripheral compartment together with elimination of the drug, while the later, slower phase is due in part to a relatively slow efflux of paclitaxel back out of that peripheral compartment.

Pregnancy & Breastfeeding

Pregnancy Category D. There isn't enough evidence from human studies to confirm the effects of paclitaxel in pregnancy, but like other cytotoxic drugs, it may harm the unborn baby if taken while pregnant. Paclitaxel should not be used while breastfeeding.

⚠️ Talk to your doctor before taking any medicine during pregnancy or while breastfeeding.

Dosage Reference

⚠️ Reference ranges from official sources only. Consult your doctor for personalized dosing.

Adults: All patients should be premedicated prior to Paclitaxel administration in order to prevent severe hypersensitivity reactions. Such premedication may consist of dexamethasone 20 mg PO administered approximately 12 and 6 hours before Paclitaxel, diphenhydramine (or its equivalent) 50 mg IV 30 to 60 minutes prior to Paclitaxel, and cimetidine (300 mg) or ranitidine (50 mg) IV 30 to 60 minutes before Paclitaxel.First-line treatment of ovarian cancer: Although alternative medication regimens for paclitaxel are under investigation at present, a combination therapy of paclitaxel and cisplatin is recommended. Depending on the duration of infusion, two different dosages are recommended for paclitaxel treatment: 175 mg/m2 of paclitaxel is administered as an intravenous infusion over a period of three hours followed thereafter by 75 mg/m2 of cisplatin and the therapy is repeated at 3-week intervals, or 135 mg/m2 of paclitaxel is administered as an intravenous infusion over a period of 24 hours followed thereafter by 75 mg/m2 of cisplatin and the therapy is repeated at 3-week intervals.Second-line treatment of ovarian cancer: The recommended dose of paclitaxel is 175 mg/m2 administered over 3 hours, with a 3-week interval between courses.Adjuvant chemotherapy in breast carcinoma: The recommended dose of paclitaxel is 175 mg/m2 administered over a period of 3 hours every 3 weeks for four courses, following AC therapy.First-line chemotherapy of breast carcinoma: When used in combination with doxorubicin (50 mg/m2), paclitaxel should be administered 24 hours after doxorubicin. The recommended dose of paclitaxel is 220 mg/m2 administered intravenously over a period of 3 hours, with a 3-week interval between courses. When used in combination with trastuzumab, the recommended dose of paclitaxel is 175 mg/m2 administered intravenously over a period of 3 hours, with a 3-week interval between courses. Paclitaxel infusion may be started the day following the first dose of trastuzumab or immediately after the subsequent doses of trastuzumab if the preceding dose of trastuzumab was well tolerated.Second-line chemotherapy of breast carcinoma: The recommended dose of paclitaxel is 175 mg/m2 administered over a period of 3 hours, with a 3-week interval between courses.Advanced non-small-cell lung cancer: The recommended dose of paclitaxel is 175 mg/m2 administered over 3 hours followed by 80 mg/m2 of cisplatin, with a 3-week interval between courses.Treatment of AIDS-related KS: The recommended dose of paclitaxel is 100 mg/m2 administered as a 3-hour intravenous infusion every two weeks.Dose adjustment: Subsequent doses of paclitaxel should be administered according to individual patient tolerance. Paclitaxel should not be re-administered until the neutrophil count is >1.5 x 109/1 (>1 x 109/1 for KS patients) and the platelet count is >100 x 109/1 (>75 x 109/1 for KS patients).

Side Effects & Interactions