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.
Samsung Medical Center, Seoul, Korea, Republic of
M D Anderson Cancer Center, Houston, Texas, United States
UCLA Medical Center, Los Angeles, California, United States
Hackensack University Medical Center, Hackensack, New Jersey, United States
Johns Hopkins University, Baltimore, Maryland, United States
Kailiang Wu, Shanghai, Shanghai, China
Beijing Friendship Hospital, Capital Medical University, Beijing, Beijing, China
Ruijin Hospital, Shanghai, Shanghai, China
University of Pittsburgh Cancer Institute - Hillman Cancer Center, Pittsburgh, Pennsylvania, United States
Carle Cancer Center NCI Community Oncology Research Program, Urbana, Illinois, United States
Marshfield Medical Center-Marshfield, Marshfield, Wisconsin, United States
Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center, Lebanon, New Hampshire, United States
City of Hope Medical Center, Duarte, California, United States
Houston Methodist, Houston, Texas, United States
University of Arkansas, Little Rock, Arkansas, United States
Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.