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.
University of Pittsburgh, Pittsburgh, Pennsylvania, United States
Penn State Milton S Hershey Medical Center, Hershey, Pennsylvania, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
University of Texas MD Anderson Cancer Center, Houston, Texas, United States
Northeast Georgia Medical Center, Gainesville, Georgia, United States
Vasicek Cancer Center at Scott & White Memorial Hospital, Temple, Texas, United States
Municipal Institution "Cherkasy Regional Oncology Dispensary" of Cherkasy Regional Council, Cherkasy, Ukraine
Fukushima Medical University Hospital, Fukushima, Japan
Memorial Sloan Kettering Bergen, Montvale, New Jersey, United States
Memorial Sloan Kettering Westchester, Harrison, New York, United States
Hartford Hospital (Data Collection Only), Hartford, Connecticut, United States
1200.93.33002 Boehringer Ingelheim Investigational Site, Dijon, France
1200.93.33001 Boehringer Ingelheim Investigational Site, Saint-Herblain cedex, France
1200.93.33003 Boehringer Ingelheim Investigational Site, Toulouse, France
University College London Hospital, London, United Kingdom
Hammersmith Hospital, London, United Kingdom
The Christie Hospital, Manchester, United Kingdom
University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States
University of Texas MD Anderson Cancer Center, Houston, Texas, United States
GSK Investigational Site, Taipei, Taiwan
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.