শুধুমাত্র তথ্যমূলক — চিকিৎসা পরামর্শ নয়। সর্বদা লাইসেন্সপ্রাপ্ত স্বাস্থ্যসেবা প্রদানকারীর পরামর্শ নিন।

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Community data Updated 2 মাস আগে

ইঙ্গিত

Non-Small Cell Lung Cancer: Gemcitabine, in combination with cisplatin, is indicated as a first-line treatment for patients with locally advanced (inoperable Stage IIIA or IIIB) or metastatic (Stage IV) non-small cell lung cancer. Gemcitabine is also indicated for the palliative treatment of adult patients with locally advanced or metastatic non-small cell lung cancer. Pancreatic Cancer: Gemcitabine is indicated for the treatment of adult patients with locally advanced or metastatic adenocarcinoma of the pancreas. It is also indicated for patients with pancreatic cancer that is refractory to 5-FU (fluorouracil). Bladder Cancer: Gemcitabine is indicated, in combination with cisplatin therapy, for the treatment of advanced bladder cancer (muscle-invasive Stage IV tumours, with or without metastases). Breast Cancer: Gemcitabine, in combination with paclitaxel, is indicated for the treatment of patients with metastatic breast cancer who have relapsed following adjuvant or neoadjuvant chemotherapy. Prior chemotherapy should have included an anthracycline, unless this was clinically contraindicated. Ovarian Cancer: Gemcitabine, in combination with carboplatin, is indicated for the treatment of patients with recurrent epithelial ovarian carcinoma who have relapsed following platinum-based therapy.

⚠️ কোনো ওষুধ গ্রহণের আগে সর্বদা নিবন্ধিত চিকিৎসকের পরামর্শ নিন।

ফার্মাকোলজি

Gemcitabine (dFdC) is converted inside cells by nucleoside kinases into its active diphosphate (dFdCDP) and triphosphate (dFdCTP) forms. Its cytotoxic effect appears to stem from two ways these forms block DNA synthesis. First, dFdCDP inhibits ribonucleotide reductase, the enzyme uniquely responsible for generating the deoxynucleoside triphosphates that DNA synthesis depends on. Blocking this enzyme lowers deoxynucleoside levels generally, and dCTP levels in particular. Second, dFdCTP competes with dCTP for incorporation into DNA, and a small amount of Gemcitabine may also be incorporated into RNA. Because intracellular dCTP is reduced, incorporation of dFdCTP into DNA is further favoured, a process known as self-potentiation. DNA polymerase epsilon is largely unable to remove Gemcitabine and repair the growing DNA strands. Once Gemcitabine is incorporated into DNA, one further nucleotide is added to the strand, after which further DNA synthesis is essentially blocked entirely, a process called masked chain termination. Following this incorporation into DNA, Gemcitabine then appears to trigger the programmed cell death process known as apoptosis.

Pregnancy & Breastfeeding

Pregnancy Category D. Gemcitabine should be used during pregnancy. It is not known whether Gemcitabine is excreted in human breast milk.

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

ডোজ নির্দেশিকা

⚠️ শুধুমাত্র সরকারি উৎস থেকে নির্দেশিকা পরিসীমা। ব্যক্তিগতকৃত ডোজের জন্য আপনার ডাক্তারের পরামর্শ নিন।

Adults: For non-small cell lung cancer, when Gemcitabine is used on its own, the recommended dose is 1000 mg/m2 given as a 30-minute intravenous infusion. This is repeated once a week for three weeks, followed by a one-week rest period, and the four-week cycle is then repeated. The dose may be reduced from one cycle to the next, or within a cycle, depending on how much toxicity the patient experiences. When used in combination with Cisplatin, Gemcitabine has been studied using two dosing regimens: one on a three-week schedule and the other on a four-week schedule. The three-week schedule used Gemcitabine 1250 mg/m2 as a 30-minute intravenous infusion on days 1 and 8 of each 21-day cycle. The dose may be reduced from one cycle to the next, or within a cycle, depending on the toxicity experienced. The four-week schedule used Gemcitabine 1000 mg/m2 as a 30-minute intravenous infusion on days 1,8, and 15 of each 28-day cycle. Here too, the dose may be reduced with each cycle or within a cycle according to the patient's toxicity. For pancreatic cancer, the recommended dose of Gemcitabine is 1000 mg/m2 given as a 30-minute intravenous infusion. This is repeated once a week for up to 7 weeks, followed by a week of rest. Later cycles consist of an injection once a week for 3 consecutive weeks out of every 4 weeks. The dose may be reduced with each cycle or within a cycle depending on the toxicity the patient experiences. For bladder cancer, when Gemcitabine is used on its own, the recommended dose is 1250 mg/m2 given as a 30-minute intravenous infusion on days 1,8 and 15 of each 28-day cycle; this 4-week cycle is then repeated. The dose may be reduced with each cycle or within a cycle according to the toxicity experienced. When used in combination with Cisplatin, the recommended dose of Gemcitabine is 1000 mg/m2 given as a 30-minute infusion on days 1,8 and 15 of each 28-day cycle. Cisplatin is given at a recommended dose of 70 mg/m2 either on day 1 after Gemcitabine or on day 2 of each 28-day cycle, and this 4-week cycle is then repeated. The dose may be reduced with each cycle or within a cycle depending on the patient's toxicity. A clinical trial found more myelosuppression when Cisplatin was used at doses of 100 mg/m2. For breast cancer, Gemcitabine is recommended in combination with Paclitaxel. Paclitaxel (175 mg/m2) is given on Day 1 as an intravenous infusion over approximately 3 hours, followed by Gemcitabine (1250 mg/m2) as a 30-minute intravenous infusion on Days 1 and 8 of each 21-day cycle. The dose may be reduced with each cycle or within a cycle depending on the toxicity experienced. Before starting the Gemcitabine plus Paclitaxel combination, patients should have an absolute granulocyte count of at least 1,500 (x106/L). For ovarian cancer, Gemcitabine is recommended in combination with Carboplatin, with Gemcitabine 1000 mg/m2 given as a 30-minute intravenous infusion on days 1 and 8 of each 21-day cycle. After Gemcitabine, Carboplatin is given on day 1 at a dose consistent with a target AUC of 4.0 mg/mL/min. The dose may be reduced with each cycle or within a cycle depending on the toxicity the patient experiences.

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