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.
Beijing Friendship Hospital, Beijing, China
Zhejiang Cancer Hospital, Hangzhou, Zhejiang, China
University of Kansas Medical Center Research Institute, Kansas City, Kansas, United States
St Vincents Hospital, Fitzroy, Victoria, Australia
Beijing Tongren Hospital, Cmu, Beijing, Beijing, China
Cancer Hospital Chinese Academy of Medical Sciences, Beijing, Beijing, China
Azienda Ospedaliera San Camillo Forlanini, Roma, Lazio, Italy
Policlinico Universitario Agostino Gemelli, Roma, Lazio, Italy
Ospedali Riuniti Di Ancona; Oncology, Ancona, Marche, Italy
Sun Yat-sen University, Guangzhou, Guangdong, China
Fred Hutch/University of Washington Cancer Consortium, Seattle, Washington, United States
Cancer Hematology Centers - Flint, Flint, Michigan, United States
Mercy Health - Perrysburg Hospital, Perrysburg, Ohio, United States
University of Alabama at Birmingham Cancer Center, Birmingham, Alabama, United States
Institut Català d'Oncologia l'Hospitalet, Hospitalet de Llobregat, Barcelona, Spain
Hospital Universitario 12 de Octubre, Madrid, Spain
Hospital Clínico Universitario Virgen de la Victoria, Málaga, Spain
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