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.
The University of Texas Health Science Center at Houston, Houston, Texas, United States
Medical University of South Carolina, Charleston, South Carolina, United States
Mary Crowley Cancer Research Centers, Dallas, Texas, United States
Arkansas Children's Hospital, Little Rock, Arkansas, United States
Nicklaus Children's Hospital (Miami Children's Health System), Miami, Florida, United States
Department of Pancreatic Surgery, Cancer Institute & Hospital, Tianjin Medical University, Tianjin, Tianjin, China
Department of Hepatobiliary Surgery, Sun Yat-Sen University Cancer Center,Sun Yat-Sen University, Guangzhou, Guangdong, China
Department of Pancreatic Surgery, Huashan Hospital, Fudan University, Shanghai, Shanghai, China
Spanish Cooperative for Digestive Tumour Therapy (TTD), Madrid, Spain
Centre hospitalo-universitaire de Beni Messous, Algiers, Algeria
City Oncology Clinic, St.-Petersburg, Russian Federation
Institut Sainte Catherine, Avignon, France
Third Affiliated Hospital of Xinjiang Medical University, Urumchi, Xinjiang, China
Stanford University, Palo Alto, California, United States
Baptist Health, Lexington, Kentucky, United States
Memorial Hospital of South Bend, South Bend, Indiana, United States
University of California, San Francisco, San Francisco, California, United States
Hospital NisA 9 de Octubre, Valencia, Spain
Zhejiang Cancer Hospital, Zhejiang, China
Hôpital Universitaire Dupuytren, Limoges, France
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