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.
Azienda Ospedaliero Bologna, Bologna, Italy
Universitätsklinikum Dresden, Dresden, Germany
Medical University of Innsbruck, Innsbruck, Austria
Tianjin Medical University Cancer Insititute and Hospital, Tianjin, Tianjin, China
Springfield Memorial Hospital, Springfield, Illinois, United States
Henry Ford Saint John Hospital - Macomb Medical, Macomb, Michigan, United States
Marshfield Medical Center - Minocqua, Minocqua, Wisconsin, United States
Parkland Health and Hospital System, Dallas, Texas, United States
Northwestern Memorial Hospital, Chicago, Illinois, United States
Massachusetts General Hospital, Boston, Massachusetts, United States
Centre Hospitalier de Longjumeau, Longjumeau, France
General University Hospital of Patras, Patras, Greece
Hospital AZ Sint-Jan, Brugge, Belgium
Emory Saint Joseph's Hospital, Atlanta, Georgia, United States
Emory University Hospital/Winship Cancer Institute, Atlanta, Georgia, United States
Nebraska Methodist Hosptial, Omaha, Nebraska, United States
Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, Indiana, United States
University of Cincinnati Cancer Institute, Cincinnati, Ohio, United States
Anhui Provincial Hospital, Hefei, Anhui, China
Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China
Jilin Cancer Hospital, Chang chun, Jilin, China
Research Site, Hochiminh, Vietnam
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