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.
Gifu University Hospital ( Site 1513), Gifu, Japan
Volgograd Regional Uronephrological Center ( Site 0870), Volzhsky, Volgogradskaya Oblast, Russian Federation
Municipal Non-profit Enterprise of Kharkiv Regional Council RCSDRPP ( Site 0965), Kharkiv, Kharkivska Oblast, Ukraine
Willis-Knighton Physician Network/Gynecologic Oncology Associates, Shreveport, Louisiana, United States
Maryland Oncology Hematology, P.A., Columbia, Maryland, United States
Fondazione Policlinico Universitario Agostino, Roma, Other, Italy
City of Hope, Duarte, California, United States
START, San Antonio, Texas, United States
University of Montreal - Centre Hospitalier de l´Université de Montréal, Montréal, Canada
Sun Yat Sen Memorial Hospital,Sun Yat sen University, Guangzhou, Guangdong, China
Istituto Tumori della Romagna IRST IRCCS, Meldola, Italy
Azienda Ospedaliera Spedali Civili, Brescia, Italy
IEO-Istituto Europeo di Oncologia, Milan, Italy
Massachusetts General Hospital, Boston, Massachusetts, United States
Duke Cancer Center, Durham, North Carolina, United States
City of Hope Cancer Center, Duarte, California, United States
HonorHealth Research Institute, Scottsdale, Arizona, United States
Virginia mason medical Center, Seattle, Washington, United States
University of Southern California, Los Angeles, California, United States
Centro Oncologico Riojano Integral (Cori), La Rioja, Argentina
Fundacao Pio XII, Barretos, Brazil
Investigational Site Number : 7920004, Ankara, Turkey
Investigational Site Number : 5280001, Rotterdam, Netherlands
Investigational Site Number : 7920003, Adana, Turkey
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