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.
St. Jude Children's Research Hospital, Memphis, Tennessee, United States
Oregon Health & Science University, Portland, Oregon, United States
The University of Kansas Cancer Center, Westwood, Kansas, United States
Mount Sinai School of Medicine, New York, New York, United States
Biotherapeutic Department of Chinese PLA General Hospital, Beijing, Beijing, China
UCLA Hematology/Oncology - Santa Monica ( Site 0014), Los Angeles, California, United States
Hartford Hospital ( Site 0057), Hartford, Connecticut, United States
Winship Cancer Institute of Emory University ( Site 0013), Atlanta, Georgia, United States
Biotherapeutic Department of Chinese PLA General Hospital, Beijing, Beijing, China
Xiangya Hospital Central South University, Changsha, Hunan, China
Fujian Provinve Cancer Hospital, Fuzhou, Fujian Provinve, China
Cancer Hospital of Guizhou Medical University, Guiyang, Guizhou, China
Jiangmen central hospital, Jiangmen, Guangdong, China
Hôpital Nord Franche-Comté, Montbéliard, France
CH Mulhouse, Mulhouse, France
University Hospital of Besançon, Besancon, France
Bayhealth Hospital Kent Campus, Dover, Delaware, United States
Marshfield Clinic-Wausau Center, Wausau, Wisconsin, United States
Riverside Methodist Hospital, Columbus, Ohio, United States
Hôpital Européen de Marseille, Marseille, France
Hôpital Pitié-Salpétrière, Paris, France
Hospices civils de Lyon, Lyon, France
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