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.
Clinical Study Site 2, Kyiv, Ukraine
Clinical Study Site 3, İzmir, Turkey
Clinical Study Site #3, São Paulo, Brazil
Medical University of South Carolina, Charleston, South Carolina, United States
Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, United States
Comprehensive Cancer Centers of Nevada, Las Vegas, Nevada, United States
The Angeles Clinic and Research Institute, Los Angeles, California, United States
MD Anderson Cancer Center, Houston, Texas, United States
Mayo Clinic Arizona, Phoenix, Arizona, United States
University of Louisville, Louisville, Kentucky, United States
The University of Hong Kong, Hong Kong, Hong Kong
UCLA Santa Monica Hematology / Oncology SC-2, Santa Monica, California, United States
Henry Ford Health System SC, Detroit, Michigan, United States
Stanford Cancer Center SC, Stanford, California, United States
Samsung Medical Center, Seoul, Korea, Republic of
Chonnam National University Hwasun Hospital, Hwasun-gun, Jeollanam-do, Korea, Republic of
Seoul National University Hospital, Seoul, Korea, Republic of
St. Vincent Anderson Regional Hospital, Anderson, Indiana, United States
IU Health Ball Memorial Hospital Cancer Center, Muncie, Indiana, United States
Community Healthcare System, Munster, Indiana, United States
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