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.
West Virginia University Hospitals - Mary Babb Randolph Cancer Center, Morgantown, West Virginia, United States
Reliant Medical Group, Inc., Worcester, Massachusetts, United States
Banner MD Anderson Cancer Ctr., Gilbert, Arizona, United States
UCLA School of Medicine, Los Angeles, California, United States
Beijing Cancer Hospital, Beijing, Beijing, China
First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui, China
Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China
Ohio State University - Wexner Medical Center, Columbus, Ohio, United States
South Texas Accelerated Research Therapeutics, San Antonio, Texas, United States
University of Michigan Health System, Ann Arbor, Michigan, United States
University of Southern California, Los Angeles, California, United States
Massachusetts General Hospital, Boston, Massachusetts, United States
Dana Farber Cancer Institute, Boston, Massachusetts, United States
University of Chicago Medical Center, Chicago, Illinois, United States
MD Anderson Cancer Center / University of Texas, Houston, Texas, United States
University of Alabama at Birmingham, Birmingham, Alabama, United States
Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, Indiana, United States
Community Regional Cancer Care, Indianapolis, Indiana, United States
IU Health Central Indiana Cancer Center, Indianapolis, Indiana, United States
Sun Yat-sen University Cancer Center, GuangZhou, Guangdong, China
Azienda Ospedaliero-Universitaria Pisana, Pisa, PI, Italy
Research Site, Wolverhampton, United Kingdom
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