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.
Massachusetts General Hospital, Boston, Massachusetts, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
Northwest Georgia Oncology Centers, Marietta, Georgia, United States
USA Mitchell Cancer Center, Mobile, Alabama, United States
University of Alabama, Birmingham, Alabama, United States
Barts and The London NHS, St Bartholomew's Hospital, London, United Kingdom
Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom
Imperial College NHS Trust, London, United Kingdom
Masonic Cancer Center - University of Minnesota, Minneapolis, Minnesota, United States
Huntsman Cancer Institute - University of Utah Health, Salt Lake City, Utah, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
Piedmont Cancer Institute, Atlanta, Georgia, United States
Winship Cancer Institute / Emory University School of Medicine, Atlanta, Georgia, United States
Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States
Rigshospitalet, Department of Oncology, Copenhagen, Denmark
Medizinische Universität Wien, Vienna, Austria
Landeskrankenhaus Salzburg, Salzburg, Austria
Nottingham University Hospitals NHS Trust - City Hospital, Nottingham, United Kingdom
Hospital Universitario 12 De Octubre, Madrid, Spain
The Christie NHS Foundation Trust, Manchester, United Kingdom
M D Anderson Cancer Center, Houston, Texas, United States
Feinstein Institutes for Medical Research - Northwell Health, Manhasset, New York, United States
Sarah Cannon Research Institute, Nashville, Tennessee, United States
VA Loma Linda Healthcare System, Loma Linda, California, United States
Clinical Site, Osaka, Japan
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