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.
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland, United States
Simmons Comprehensive Cancer Center at University of Texas Southwestern Medical Center - Dallas, Dallas, Texas, United States
Driscoll Children's Hospital, Corpus Christi, Texas, United States
Stanford Cancer Center, Stanford, California, United States
Yale Cancer Center, New Haven, Connecticut, United States
AFLAC Cancer Center and Blood Disorders Service of Children's Healthcare of Atlanta - Scottish Rite Campus, Atlanta, Georgia, United States
St. James's Hospital, Leeds, England, United Kingdom
Johns Hopkins Oncology Center, Baltimore, Maryland, United States
Duke Comprehensive Cancer Center, Durham, North Carolina, United States
USC/Norris Comprehensive Cancer Center, Los Angeles, California, United States
Centro di Riferimento Oncologico - Aviano, Aviano, Italy
University of Arkansas for Medical Sciences/MIRT, Little Rock, Arkansas, United States
Marlene & Stewart Greenebaum Cancer Center, University of Maryland, Baltimore, Maryland, United States
Marlene & Stewart Greenebaum Cancer Center, University of Maryland, Baltimore, Maryland, United States
University of Arkansas for Medical Sciences/MIRT, Little Rock, Arkansas, United States
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