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|Product Name:||Paclitaxel Concentrate For Infusion||Composition:||Each 5ml Contains:30 Mg Paclitaxel|
|Indications:||1.The Palliative Treatment Of Stage 3 Or 4 Advanced Local Carcinoma Of The Ovary After Surgical Resection, In Combination With Cisplatin. 2. The Palliative Management Of Metastatic Carcinoma Of The Ovary After Failure Of First Line Or Subsequent Chemother||Storage Instructions:||Store At Room Temperature Not Exceeding 25°C.|
|Expiration Date:||2 Years|
Paclitaxel Concentrate for Infusion 30mg/5ml Anticancer medicine
Each 5 mL vial contains 30 mg paclitaxel and 49,7% v/v of dehydrated alcohol.
Paclitaxel is an antimicrotubule agent that promotes the assembly of microtubules from tubulin dimers and stabilizes microtubules by preventing depolymerization. This stability results in the inhibition of the normal dynamic reorganisation of the microtubule network that is essential for vital interphase and mitotic cellular functions. In addition, paclitaxel induces abnormal arrays or bundles of microtubules throughout the cell cycle and multiple asters of microtubules during mitosis.
Following intravenous administration, paclitaxel exhibits a biphasic decline in plasma concentrations. The initial rapid decline represents distribution to the peripheral compartment and elimination; the later phase is due, in part, to a relatively slow efflux of paclitaxel from the peripheral compartment. In patients treated with doses of 135 and 175 mg/m² given as 3 and 24 hour infusions, mean terminal half-life has ranged from 3,0 to 52,7 hours. Mean values for total body clearance ranged from 11.6 to 24 L/h/m². Mean steady state volume of distribution has ranged from 198 to 688 L/m², indicating extensive extravascular distribution and/or tissue binding.
The pharmacokinetics of paclitaxel are non-linear. There is a disproportionately large increase in Cmax and AUC with increasing dose, accompanied by an apparent dose-related decrease in total body clearance. These findings are most readily observed in patients in whom, high plasma concentrations of paclitaxel are achieved. Saturable processes in distribution and elimination/metabolism may account for these findings.
There was no evidence of accumulation of paclitaxel with multiple treatment course.
In vitro studies of binding to human serum proteins, using paclitaxel concentrations ranging from 0,1 to 50 micrograms/mL, indicate that, on average, 89% of drug is bound. The presence of cimetidine, ranitidine, dexamethasone or diphenhydramine did not affect protein binding of paclitaxel.
The disposition of paclitaxel has not been fully elucidated in humans. After intravenous administration of paclitaxel, mean values of cumulative urinary recovery of unchanged drug ranged from 1.3 to 12.6% of the dose, indicating extensive non-renal clearance.
Hepatic metabolism and biliary clearance may be the principal mechanism for disposition of paclitaxel. Paclitaxel is metabolized primarily by cytochrome P450 enzymes. Hydroxylated metabolites have been demonstrated to be the principal metabolites. The formation of 6 alpha-hydroxypaclitaxel ,3’-p-hydroxypaclitaxel and 6 alpha,3’-p-dihydroxypaclitaxel is catalysed by CYP2C8, 3A4 and both 2C8 and 3A4 respectively. The effect of the renal or hepatic dysfunction on the disposition of paclitaxel has not been investigated. The clearance of paclitaxel was not affected by cimetidine pre-treatment. Ketoconazole may inhibit the metabolism of paclitaxel. Plasma levels of doxorubicin and doxorubicinol may be increased when paclitaxel and doxorubicin are used in combination.
1.The palliative treatment of stage 3 or 4 advanced local carcinoma of the ovary after surgical resection, in combination with cisplatin.
2.The palliative management of metastatic carcinoma of the ovary after failure of first line or subsequent chemotherapy.
3.The treatment of metastatic carcinoma of the breast after failure of combination chemotherapy or relapse within 6 months of adjuvant chemotherapy. Prior therapy should have included an anthracycline unless clinically contra-indicated.4. Palliative treatment of advanced non-small cell lung cancer in patients who are not candidates for potentially curative surgery and/or radiation therapy.
DOSAGE AND DIRECTIONS FOR USE
Primary treatment of ovarian carcinoma: a combination regimen consisting of Paclitaxel 135 mg/m² administered over 24 hours, followed by cisplatin 75 mg/m², every 3 weeks. Paclitaxel should be administered before cisplatin.
Indication 2 and 3:
Secondary treatment of ovarian carcinoma: Paclitaxel at a dose of 175 mg/m² administered intravenously over 3 hours every 3 weeks has been shown to be effective in patients with metastatic carcinoma of the ovary or breast after the failure of first line or subsequent chemotherapy.
Palliative treatment of advanced non-small cell lung carcinoma: the recommended dose of Paclitaxel is 175 mg/m²administered over a period of 3 hours; followed by a platinum compound , with a 3 week interval between courses.
Paclitaxel should not be readministered until the neutrophil count is at least 1 500/mm³ and the platelet count is at least 100 000/mm³. Patients who experience severe neutropenia (neutrophil count <500/mm³) or moderate to severe peripheral neuropathy should receive a dose reduction of 20% for subsequent courses (see SIDE-EFFECTS AND SPECIAL PRECAUTIONS). The incidence and severity of neurotoxicity and haematologic toxicity increases with dose.
All patients must be premedicated with corticosteroids, antihistamines, and H2 antagonists prior to Paclitaxel administration, e.g. dexamethasone 20 mg orally approximately 12 and 6 hours before Paclitaxel, promethazine 25 mg IV 30 to 60 minutes prior to Paclitaxel, and cimetidine 300 mg or ranitidine 50 mg, IV 30 to 60 minutes before Paclitaxel.
Paclitaxel should be administered through an in-line filter with a microporous membrane not greater that 0,22 microm.
Directions for Use/Handling
Handling: Caution should be exercised when handling Paclitaxel. Dilution should be carried out by trained personnel in a designated area. Adequate protective gloves should be worn. Precautions should be taken to avoid contact with the skin, and mucous membranes. Following topical exposure, tingling, burning and redness have been observed. In the event of contact with the skin, the area should be washed with soap and water. In the event of contact with the mucous membranes, these should be flushed thoroughly with water. Upon inhalation, dyspnoea, chest pain, burning eyes, sore throat and nausea have been reported.
Preparation for IV Administration: Paclitaxel must be diluted prior to infusion. Paclitaxel should be diluted in 0,9% Sodium Chloride Injection, or 5% Dextrose Injection, or 5% Dextrose and 0,9% Sodium Chloride Injection, or 5% Dextrose in Ringer's Injection to a final concentration of 0,3 to 1,2 mg/mL. The prepared solutions are physically and chemically stable for up to 27 hours at ambient temperature (approximately 25°C) and room lighting conditions.
Parenteral drug products should be inspected visually for particulate matter and discolouration prior to administration whenever solution and container permit.
Upon preparation, solutions may show haziness, which is attributed to the formulation vehicle. Paclitaxel should be administered through an in-line filter with a microporous membrane not greater than 0,22 microm. No significant losses in potency have been noted following delivery of the solution through IV tubing containing an in-line filter.
In order to minimise patient exposure to the plasticiser DEHP [di-(2-ethylexyl)phthalate], which may be leached from plasticised PVC infusion bags or sets, diluted Paclitaxel solutions should preferably be stored in bottles (glass, polypropylene) or plastic bags (polypropylene, polyolefin) and administered through polyethylene-lined administration sets. Use of filter devices which incorporate short inlet and/or outlet plasticised PVC tubing has not resulted in significant leaching of DEHP.
Disposal: All items used for reconstitution, administration or otherwise coming into contact with Paclitaxel should undergo disposal according to local guidelines for the handling of cytotoxic compounds.
Paclitaxel is contra-indicated in patients who have a history of severe hypersensitivity reactions to Paclitaxel or other drugs formulated with polyoxyethylated castor oil.
Paclitaxel should not be used in patients with baseline neutrophils <1 500/mm³.
PREGNANCY AND LACTATION
Paclitaxel has been shown to be embryotoxic, foetotoxic and to decrease fertility in animal studies.
There is no information on the use of Paclitaxel in pregnant women. Paclitaxelmay cause foetal harm when administered to pregnant women. Paclitaxelshould not be used during pregnancy. Women of childbearing potential should be advised to avoid becoming pregnant during therapy with Paclitaxel, and to inform the treating physician immediately should this occur.
It is not known whether Paclitaxel is excreted in human milk. Breast feeding should be discontinued for the duration of Paclitaxel therapy.
SIDE-EFFECTS AND SPECIAL PRECAUTIONS
The frequency and severity of adverse events are generally similar between patients receiving Paclitaxel for the treatment of ovarian, breast or lung carcinoma. None of the observed toxicities were clearly influenced by age.
Safety of the Paclitaxel/platinum combination has been evaluated in a randomised trial in ovarian carcinoma and 2 phase lll trials in non-small cell lung carcinoma. Unless otherwise mentioned the combination of Paclitaxelwith platinum agents did not result in clinically relevant changes to the safety profile of single agent Paclitaxel.
Bone marrow suppression and peripheral neuropathy are the principal dose-related adverse effects associated with Paclitaxel. Myelosuppression is less frequent and less severe with a 3-hour infusion than with a 24 hour infusion schedule. The recommended Paclitaxel/cisplatin regimen for the primary treatment of ovarian cancer caused more severe myelosuppression than single dose Paclitaxel using the recommended schedule of 175 mg/m²over 3 hour infusion. There was no increase in clinical sequelae, however.
Compared to 24-hour infusion schedules, neutropenia is less common when Paclitaxel is given as a 3-hour infusion. Neutropenia is generally rapidly reversible. Severe neutropenia occurs in some patients. Neutropenia is not more frequent or severe in patients who receive prior radiation therapy. Likewise, neutropenia does not appear to be affected by treatment duration or cumulative exposure. Infectious episodes have been reported in some patients but none have resulted in fatality.
Thrombocytopenia occurs in a few patients. Severe thrombocytopenia is observed only during the first two courses. Although bleeding episodes occur in some patients, no patient has required platelet transfusion.
Anaemia has been observed in the majority of the patients. Incidence and severity of anaemia is related to baseline haemoglobin status. Red cell transfusions are required in some patients.
Paclitaxel therapy should not be administered to patients with baseline neutrophil counts of less than 1,500 cells/mm³. In order to monitor the occurrence of myelotoxicity, it is recommended that frequent peripheral blood cell counts be performed on all patients receiving Paclitaxel. Patients should not be retreated with subsequent cycles of Paclitaxel until neutrophils recover to a level >1,500 cells/mm³ and platelets recover to a level >100,000 cells/mm³. In the case of severe neutropenia (<500 cells/mm³ for seven days or more) during a course of Paclitaxel therapy, a 20% reduction in dose for subsequent courses of therapy is recommended.
Hypersensitivity reactions may occur requiring therapeutic intervention and/or early discontinuation of Paclitaxel infusion despite premedication. Severe symptoms occur within the first hour of Paclitaxel infusion. Dyspnoea, flushing, chest pains and tachycardia are the most frequent manifestations.
Paclitaxel dosage or schedule has no effect on the frequency of hypersensitivity reactions.
Besides the few patients with severe hypersensitivity reactions, other patients experience minor manifestations compatible with hypersensitivity reactions. The most frequent minor manifestations are flushing, rash and hypotension.
Patients with a history of severe hypersensitivity reactions to products containing Cremophor EL (e.g. cyclosporin for injection concentrate and teniposide for injection concentrate) should not be treated with Paclitaxel. In order to avoid the occurrence of severe hypersensitivity reactions, all patients treated with Paclitaxel should be premedicated with corticosteroids (such as dexamethasone), promethazine and H2 antagonists (such as cimetidine or ranitidine). Minor symptoms such as flushing, skin reaction, dyspnoea, hypotension or tachycardia do not require interruption of therapy. However, severe reactions, such as hypotension requiring treatment, dyspnoea requiring bronchodilators, angioedema or generalised urticaria require immediate discontinuation of Paclitaxel and appropriate emergency therapy. Patients who have developed severe hypersensitivity reactions should not be rechallenged with Paclitaxel.
Hypotension and bradycardia have been observed during administration of Paclitaxel, but generally do not require treatment. Frequent vital sign monitoring, particularly during the first hour of Paclitaxel infusion, is recommended. Continuous cardiac monitoring is not required except for patients with serious conduction abnormalities. (see "WARNINGS" section) Cases of myocardial infarction have been reported. Congestive heart failure has been reported typically in patients who have received other chemotherapy, notably anthracyclines.
Patients may experience severe cardiovascular events possibly related to Paclitaxel administration. Included are hypertension, venous thrombosis, ventricular tachycardia, and atrioventricular conduction block.
ECG alterations are experienced by some patients.
The most frequently reported ECG modifications are non-specific repolarization abnormalities, sinus tachycardia and premature beats. The relationship between Paclitaxeladministration and ECG alterations is not clear.
Peripheral neuropathy occurs and is dose dependent. Neurologic symptoms may occur following the first course and the frequency of symptoms may increase with increasing exposure to Paclitaxel. Sensory symptoms have usually improved or resolved within several months of Paclitaxel discontinuation. Pre-existing neuropathies resulting from prior therapies are not a contra-indication for Paclitaxel therapy.
Paclitaxel contains dehydrated alcohol, 396 mg/ mL. Consideration should be given to possible CNS and other effects of alcohol.
Although the occurrence of peripheral neuropathy is frequent, the development of moderate to severe symptomatology is unusual and requires a dose reduction of 20% for all subsequent courses of Paclitaxel.
In non-small cell lung carcinoma patients, the administration of Paclitaxel in combination with cisplatin resulted in a greater incidence of neurotoxicity than usually seen in patients receiving single agent Paclitaxel.
Besides peripheral neuropathy, other rare neurologic manifestations are grand mal seizure, syncope, ataxia and neuroencephalopathy. Reports of motor neuropathy with resultant minor distal weakness and autonomic neuropathy resulting in paralytic ileus and orthostatic hypotension have appeared. Optic nerve and/or visual disturbances (scintillating scotomata) have also been reported, particularly in patients who have received higher doses than recommended. These effects generally have been reversible. Ototoxicity has been reported.
Arthralgia/myalgia usually consisting of pain in the large joints of the arms and legs occurs but is usually mild. The symptoms are usually transient occurring two or three days after Paclitaxel administration and resolving within a few days.
There is no evidence that the toxicity of Paclitaxel is enhanced when given as a 3-hour infusion in patients with elevated liver enzymes, but no data are available for patients with severe baseline cholestasis.
When Paclitaxel is given as a 24-hour infusion to patients with moderate to severe hepatic impairment, increased myelosuppression may be seen as compared to patients with mildly elevated liver function tests given 24-hour infusions.
Analysis restricted to patients with normal baseline liver function, shows instances of elevated bilirubin elevated alkaline phosphate, and elevated AST (SGOT). Hepatic necrosis and hepatic encephalopathy leading to death have been reported.
Other Clinical Events:
Alopecia has been observed in almost all of the patients. Transient and mild nail and skin changes have been observed. Rare reports of skin abnormalities related to radiation recall have been received. Gastrointestinal side effects such as nausea/vomiting, diarrhoea and mucositis have been reported. These manifestations are usually mild to moderate at the recommended dose.
Fibrotic phlebitis has been reported.
Neutropenic enterocolitis has been reported. Radiation pneumonitis has also been reported in patients receiving concurrent radiotherapy.
Extravasation during intravenous administration may lead to oedema, pain, erythema and induration and ulceration. Extravasation can result in cellulitis. Skin discolouration may also occur. Recurrence of skin reactions at a site of previous extravasation following administration of Paclitaxel at a different site i.e. "recall reaction" has been reported. A specific treatment for extravasation reactions is unknown at this time.
Bowel obstructions/perforations and ischemic colitis have been reported in patients treated with paclitaxel.
Interaction with other medicaments and other forms of interaction:
The recommended regimen of Paclitaxel administration for the primary treatment of ovarian carcinoma is for Paclitaxel to be given before cisplatin. When Paclitaxel is given before cisplatin, the safety profile of Paclitaxel is consistent with that reported for single agent use. When Paclitaxelwas given after cisplatin, patients showed a more profound myelosuppression and an approximately 20% decrease in paclitaxel clearance.
Medications concomitantly administered with Paclitaxel(e.g., corticosteroids, antihistamines, and H2 antagonists) did not appear to interact adversely; however, possible interactions of Paclitaxelwith concomitantly administered medications have not been formally investigated.
Based on in vitro data, there is the possibility of an inhibition of Paclitaxelmetabolism in patients treated with ketoconazole. As a result, caution should be exercised when treating patients with Paclitaxelwhen they are receiving ketoconazole as concomitant therapy.
Plasma levels of doxorubicin and doxorubicinol may be increased when paclitaxel and doxorubicin are used in combination.
The metabolism of paclitaxel is catalysed by cytochrome P450 isoenzymes CYP2C8 and CYP3A4. In the absence of formal clinical drug interaction studies, caution should be exercised when administering Paclitaxel concomitantly with known substrates or inhibitors of these isoenzymes.
Contact of the undiluted concentrate with plasticized polyvinyl chloride (PVC) equipment or devices used to prepare solutions for infusion is not recommended. In order to minimise patient exposure to the plasticizer DEHP [di-(2-ethylhexyl)phthalate], which may be leached from PVC infusion bags or sets, diluted Paclitaxelsolutions should preferably be stored in bottles (glass, polypropylene) or plastic bags (polypropylene, polyolefin) and administered through polyethylene-lined administration sets.
Paclitaxelshould be administered through an in-line filter with a microporous membrane not greater that 0.22 microns. Use of filter devices such as IVEX-2 filters which incorporate short inlet and outlet PVC-coated tubing has not resulted in significant leaching of DEHP.
The safety and effectiveness of Paclitaxelin children have not been established.
Store at room temperature not exceeding 25°C.
After first use any unused concentrate may be stored at room temperature not exceeding 25°C for up to 28 days.
Solutions for infusion prepared as recommended in bottles (glass, polypropylene) or plastic bags (polypropylene, polyolefin) and administered through polyethylene-lined administration sets, are stable at ambient temperature (approximately 25°C) and lighting conditions for up to 27 hours.
To be kept in outer container until required. Protect from light.
KEEP OUT OF REACH OF CHILDREN.