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.
Local Institution, Dublin, Ireland
Karmanos Cancer Institute, Detroit, Michigan, United States
National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland, United States
National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland, United States
University Hospital for Lung Diseases, Zagreb, Croatia
FILO French Innovative Leukemia Organization, Tours Cedex, France
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
North Shore Medical Center, Peabody, Massachusetts, United States
Massachusetts General Hospital, Boston, Massachusetts, United States
Dana Farber Cancer Institute, Boston, Massachusetts, United States
Washington University, St. Louis, Missouri, United States
MD Anderson Cancer Center, Houston, Texas, United States
Boca Raton Regional Hospital, Boca Raton, Florida, United States
Mason District Hospital, Havana, Illinois, United States
Longmont United Hospital, Longmont, Colorado, United States
Penn State Hershey Cancer Institute, Hershey, Pennsylvania, United States
University of Miami, Miami, Florida, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.