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.
Chu de Meaux, Meaux, France
Clinique CHC MontLégia, Liège, Belgium
CHU Dinant Godinne - UCL Namur - YVOIR, Yvoir, Belgium
UCLA Health, Santa Monica, California, United States
Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States
Boca Raton Regional Hospital / Lynn Cancer Institute, Boca Raton, Florida, United States
Seoul National University Hospital, Seoul, Daehak-ro, Jongno-gu, Korea, Republic of
Princess Margaret Cancer Centre, Toronto, Ontario, Canada
Memorial Sloan Kettering Bergen (Limited Protocol Activities), Montvale, New Jersey, United States
Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities), Basking Ridge, New Jersey, United States
Memorial Sloan Kettering Monmouth (Limited Protocol Activities), Middletown, New Jersey, United States
Hematology Center after prof. R. Yeolyan, Yerevan, Armenia
National Center of Oncology named after V.A. Fanarjian, Yerevan, Armenia
Optimum Research (Southwest Women's Oncology Center), Albuquerque, New Mexico, United States
M D Anderson Cancer Center, Houston, Texas, United States
Highlands Oncology Group, Fayetteville, Arkansas, United States
University of California LA, Los Angeles, California, United States
Advent Health Cancer Institute, Orlando, Florida, United States
The First Hospital of China Medical University, Shenyang, Liaoning, China
Anhui Provincial Hospital ( Site 0140), Hefei, Anhui, China
Beijing Cancer Hospital ( Site 0138), Beijing, Beijing, China
Peking Union Medical College Hospital ( Site 0150), Beijing, Beijing, China
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