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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 en: | Gynecol Oncol |
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Autores principales: | , , , , , , , , , |
Formato: | Artigo |
Lenguaje: | Inglês |
Publicado: |
2012
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Materias: | |
Acceso en línea: | 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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