A phase I study with an expanded cohort to assess feasibility of intravenous docetaxel, intraperitoneal carboplatin and intraperitoneal paclitaxel in patients with previously untreated ovarian, fallopian tube or primary peritoneal carcinoma: A Gynecologic Oncology Group Study

OBJECTIVE: To define the maximum tolerated dose (MTD) and assess the feasibility of intravenous (IV) docetaxel, intraperitoneal (IP) carboplatin and IP paclitaxel in women with Stage II-IV untreated ovarian, fallopian tube or primary peritoneal carcinoma. METHODS: Patients received docetaxel (55-75...

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Publicado no:Gynecol Oncol
Main Authors: Gould, Natalie, Sill, Michael W., Mannel, Robert S., Thaker, Premal H., DiSilvestro, Paul A., Waggoner, Steven E., Yamada, S. Diane, Armstrong, Deborah K., Fracasso, Paula M., Walker, Joan L.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4527869/
https://ncbi.nlm.nih.gov/pubmed/22943879
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ygyno.2012.08.037
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