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.
Mayo Clinic Hospital, Scottsdale, Arizona, United States
University of Colorado Cancer Center, Aurora, Colorado, United States
New York University, New York, New York, United States
UCLH, London, United Kingdom
The Christie, Manchester, United Kingdom
East and North Herts NHS Foundation Trust, Northwood, United Kingdom
Allegheny General Hospital, Pittsburgh, Pennsylvania, United States
Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States
Baylor College of Medicine - Baylor Clinic, Houston, Texas, United States
Stanford Cancer Institute; Hematology, Palo Alto, California, United States
Georgetown University Medical Center, Washington, District of Columbia, United States
Columbia University Medical Center, New York, New York, United States
The University of Arizona Cancer Center, Tucson, Arizona, United States
UCSF Medical Center at Mission Bay, San Francisco, California, United States
Georgetown University Medical Center, Washington, District of Columbia, United States
Yale University, New Haven, Connecticut, United States
Hematology - Oncology Associates of Treasure Coast, Port Saint Lucie, Florida, United States
The Methodist Hospital, Houston, Texas, United States
MD Anderson Cancer Center at Cooper, Camden, New Jersey, United States
MD Anderson Cancer Center at Cooper, Camden, New Jersey, United States
Baylor College of Medicine, Houston, Texas, United States
Baylor St Luke's Medical Center, Houston, Texas, United States
Sun Yat-sen University Cancer Center, Guangzhou, Please Select, China
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