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.
National Guard Health Affairs, Riyadh, Saudi Arabia
IASO General Hospital of Athens, 1st Dept. of Medical Oncology, Athens, Greece
University General Hospital of Alexandroupolis, Dept. of Medical Oncology, Alexandroupolis, Greece
Metaxa's Anticancer Hospital of Piraeus, 1st Dept. of Medical Oncology, Piraeus, Greece
Washington University, Saint Louis, Missouri, United States
Hillman Cancer Center, Pittsburgh, Pennsylvania, United States
UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California, United States
Huntsman Cancer Center, University of Utah, Salt Lake City, Utah, United States
MacroGenics, Incorporated, South San Francisco, California, United States
Fox Chase Cancer Center - Philadelphia, Philadelphia, Pennsylvania, United States
Sanofi-Aventis Investigational Site Number 840033, San Diego, California, United States
Sanofi-Aventis Investigational Site Number 840036, Seattle, Washington, United States
Sanofi-Aventis Investigational Site Number 840020, Bethlehem, Pennsylvania, United States
Akita University Hosipital, Akita, Japan
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., Newport News, Virginia, United States
Sismanogleio General Hospital, 1st, 2nd Dep of Pulmonary Diseases, Athens, Greece
"Laikon" General Hospital, Medical Oncology Unit, Propedeutic Dep of Internal Medicine, Athens, Greece
IASO" General Hospital of Athens, 1st Dep of Medical Oncology, Athens, Greece
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