作者: Michael J. Glantz , Alixis Van Horn , Rebecca Fisher , Marc C. Chamberlain
DOI: 10.1002/CNCR.24921
关键词: Gastroenterology 、 Surgery 、 Progression-free survival 、 Methotrexate 、 Performance status 、 Internal medicine 、 Medicine 、 Antimetabolite 、 Cytarabine 、 Route of administration 、 Neoplastic meningitis 、 Chemotherapy
摘要: BACKGROUND: A study was undertaken to determine whether route (intraventricular vs intralumbar) of intracerebrospinal fluid (intra-CSF) drug administration influences progression-free survival in the treatment patients with neoplastic meningitis, which occurs 1% 5% known cancer. Currently available options result modest responses, is part a reflection obstacles delivery into leptomeningeal space. METHODS: One hundred clinically and cytologically or radiographically documented meningitis because solid cancers received intra-CSF liposomal cytarabine methotrexate as specified randomized phase 4 trial. The 2 arms were well balanced for demographic tumor-related characteristics prognostic importance, including age, performance status, tumor type, extent systemic other central nervous system (CNS) disease, prior CNS therapy, concurrent chemotherapy. RESULTS: One treated (52 sustained-release cytarabine, 48 methotrexate). Progression-free (the primary endpoint) identical between all 100 (35 37.5 days, P = .79). When examined function chemotherapy (lumbar ventricular), there no difference (29 43 .35). For methotrexate, however, statistically significant favoring receiving intraventricular therapy (19 .048). CONCLUSIONS: Site relevant short half-life drugs such methotrexate. Cancer 2010. © 2010 American Society.