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.
Robert H. Lurie Comprehensive Cancer Center at Northwestern University, Chicago, Illinois, United States
Institut Jules Bordet, Brussels (Bruxelles), Belgium
St. Johannes Hospital - Medical Klinik II, Duisburg, Germany
Universitaetsklinikum Halle, Halle (Saale), Germany
Oncology Institute of Southern Switzerland, Bellinzona, Switzerland
Inselspital, Bern, Bern, Switzerland
Ratisches Kantons und Regionalspital, Chur, Switzerland
Klinikum der Stadt Mannheim, Mannheim, Germany
Universitair Ziekenhuis Antwerpen, Edegem, Belgium
Aarhus Universitetshospital - Aarhus Sygehus, Aarhus, Denmark
Herbert Irving Comprehensive Cancer Center at Columbia University, New York, New York, United States
Children's Oncology Group, Arcadia, California, United States
University of Chicago Comprehensive Cancer Center, Chicago, Illinois, United States
University of Chicago Comprehensive Cancer Center, Chicago, Illinois, United States
Children's Oncology Group, Arcadia, California, United States
Children's Oncology Group, Arcadia, California, United States
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