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.
M D Anderson Cancer Center, Houston, Texas, United States
Mayo Clinic in Rochester, Rochester, Minnesota, United States
Emory University Hospital/Winship Cancer Institute, Atlanta, Georgia, United States
Alaska Oncology and Hematology LLC, Anchorage, Alaska, United States
Cancer & Blood Specialty Clinic, Los Alamitos, California, United States
Moores Cancer Center at the UC San Diego Health, San Diego, California, United States
Oncology Consultants, Houston, Texas, United States
Miami Cancer Institute, Miami, Florida, United States
University of Oklahoma - Health Sciences Center, Oklahoma City, Oklahoma, United States
Methodist Transplant Physicians, Dallas, Texas, United States
MD Anderson Cancer Center - Unit 429, Houston, Texas, United States
Renovatio Clinical - CENTRAL SITE, The Woodlands, Texas, United States
Barts Health NHS Trust, London, London, Greater, United Kingdom
The University of Michigan Rogel Cancer Center, Ann Arbor, Michigan, United States
Indiana University Melvin & Bren Simon Cancer Center, Indianapolis, Indiana, United States
Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, North Carolina, United States
St. Jude Children's Research Hospital, Memphis, Tennessee, United States
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