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.
Local Institution - 0001, Anchorage, Alaska, United States
Local Institution - 0115, Fresno, California, United States
St Joseph Heritage Healthcare, Santa Rosa, California, United States
Cancer Hospital Chinese Academy of Medical Sciences, Beijing, Beijing, China
Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China
Zhongshan Hospital Affiliated to Fudan University, Shanghai, Shanghai, China
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician, Tokyo, Japan
Hospital Universitario Virgen de la Arrixaca, El Palmar, Murcia, Spain
Hospital Universitario de Canarias, La Laguna, Canarias, Spain
Institut Català d'Oncologia. Hospital Universitario Germans Trias i Pujol, Badalona, Barcelona, Spain
Cliniques Universitaires Saint-Luc, Brussels, Woluwe-Saint-Lambert, Belgium
Children's Health Ireland Crumlin, Dublin, Ireland
Schneider Children's Medical Center, Petach Tikva, Israel
Centre Léon Bérard, Dpt Medecine & INSERM, Lyon, France
Gustave Roussy Cancer Center, Villejuif, France
St George's University of London, Institute of Infection and Immunity, London, United Kingdom
Memorial Regional Hospital, Hollywood, Florida, United States
Local Institution - 0151, Baltimore, Maryland, United States
Local Institution - 0006, Boston, Massachusetts, United States
City of Hope Medical Center, Duarte, California, United States
City of Hope Upland, Upland, California, United States
Comprehensive Blood and Cancer Center, Bakersfield, California, United States
Winship Cancer Institute of Emory University, Atlanta, Georgia, United States
Montefiore Cancer Center, Bronx, New York, United States
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