A semisynthetic derivative of podophyllotoxin that exhibits antitumor activity. Etoposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA. This complex induces breaks in double stranded DNA and prevents repair by topoisomerase II binding. Accumulated breaks in DNA prevent entry into the mitotic phase of cell division, and lead to cell death. Etoposide acts primarily in the G2 and S phases of the cell cycle.
For use in combination with other chemotherapeutic agents in the treatment of refractory testicular tumors and as first line treatment in patients with small cell lung cancer. Also used to treat other malignancies such as lymphoma, non-lymphocytic leukemia, and glioblastoma multiforme.
CCOP - Illinois Oncology Research Association, Peoria, Illinois, United States
CCOP - Carle Cancer Center, Urbana, Illinois, United States
CCOP - Iowa Oncology Research Association, Des Moines, Iowa, United States
Hope Children's Hospital, Oak Lawn, Illinois, United States
Arizona Cancer Center, Tucson, Arizona, United States
Saint Jude Midwest Affiliate, Peoria, Illinois, United States
University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States
University of California San Diego Cancer Center, La Jolla, California, United States
Marlene & Stewart Greenebaum Cancer Center, University of Maryland, Baltimore, Maryland, United States
Memorial Sloan-Kettering Cancer Center, New York, New York, United States
Hotel Dieu de Paris, Paris, France
A.Z. St. Jan, Brugge, Belgium
Innsbruck Universitaetsklinik, Innsbruck, Austria
Memorial Sloan-Kettering Cancer Center, New York, New York, United States
Klinikum der J.W. Goethe Universitaet, Frankfurt, Germany
Medizinische Hochschule Hannover, Hannover, Germany
Royal Infirmary, Glasgow, Scotland, United Kingdom
Hackensack University Medical Center, Hackensack, New Jersey, United States
Riverview Medical Center - Booker Cancer Center, Red Bank, New Jersey, United States
University of Nebraska Medical Center, Omaha, Nebraska, United States
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