Gemcitabine is a nucleoside analog and a chemotherapeutic agent. It was originally investigated for its antiviral effects, but it is now used as an anticancer therapy for various cancers. Gemcitabine is a cytidine analog with two fluorine atoms replacing the hydroxyl on the ribose. As a prodrug, gemcitabine is transformed into its active metabolites that work by replacing the building blocks of nucleic acids during DNA elongation, arresting tumour growth and promoting apoptosis of malignant cells. The structure, metabolism, and mechanism of action of gemcitabine are similar to cytarabine, but gemcitabine has a wider spectrum of antitumour activity.
Gemcitabine is marketed as Gemzar and it is available as intravenous injection. It is approved by the FDA to treat advanced ovarian cancer in combination with carboplatin, metastatic breast cancer in combination with paclitaxel, non-small cell lung cancer in combination with cisplatin, and pancreatic cancer as monotherapy. It is also being investigated in other cancer and tumour types.
Gemcitabine is a chemotherapeutic agent used as monotherapy or in combination with other anticancer agents.
In combination with carboplatin, it is indicated for the treatment of advanced ovarian cancer that has relapsed at least 6 months after completion of platinum-based therapy.
Gemcitabine in combination with paclitaxel is indicated for the first-line treatment of patients with metastatic breast cancer after failure of prior anthracycline-containing adjuvant chemotherapy, unless anthracyclines were clinically contraindicated.
In combination with cisplatin, gemcitabine is indicated for the first-line treatment of patients with inoperable, locally advanced (Stage IIIA or IIIB) or metastatic (Stage IV) non-small cell lung cancer (NSCLC). Dual therapy with cisplatin is also used to treat patients with Stage IV (locally advanced or metastatic) transitional cell carcinoma (TCC) of the bladder.
Gemcitabine is indicated as first-line treatment for patients with locally advanced (nonresectable Stage II or Stage III) or metastatic (Stage IV) adenocarcinoma of the pancreas. Gemcitabine is indicated for patients previously treated with fluorouracil.
Donald W. Hill, MD, Casa Grande, Arizona, United States
Norwalk Hospital, Norwalk, Connecticut, United States
New Jersey Hematology Oncology Associates, Brick, New Jersey, United States
Research Site, Nashville, Tennessee, United States
Washington University, St. Louis, Missouri, United States
University of Cincinnati, Cincinnati, Ohio, United States
The Queen's Medical Center Cancer Center, Honolulu, Hawaii, United States
Front Range Cancer Specialists, Ft. Collins, Colorado, United States
Bronx River Medical Associates, P.C., Bronx, New York, United States
Sotiria" General Hospital, 1st, 3rd, 8th Dep of Pulmonary Diseases, Athens, Greece
"Metaxa's" Anticancer Hospital of Piraeus,1st Dep of Medical Oncology, Piraeus, Greece
"Theagenion" Anticancer Hospital of Thessaloniki, Thessaloniki, Greece
Ipoh Specialist Centre, Ipoh, Malaysia
Johor Specialist Centre, Johor Bahru, Malaysia
Tung Shin Hospital, Kuala Lumpur, Malaysia
Desert Regional Medical Center, Palm Springs, California, United States
Bellevue Hospital, New York, New York, United States
New York University Cancer Center, New York, New York, United States
1. Department of Medical-Surgical Specialties and Public Health, Section of Urology and Andrology, University of Perugia - Italy, Perugia, Italy
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