To assess time to progression in patients with unresectable HCC receiving intra-arterial chemotherapy with cisplatin and mitomycin-C wk 7 of each cycle [clinicaltrials_resource:2f696e908d15932401d049fc0e52ebfc]
CDDP 60mg/m2 + Mitomycin-C 12mg/m2
clinicaltrials_vocabulary:primary outcome [clinicaltrials_vocabulary:clinicaltrials_vocabulary:primary-outcome]
To assess time to progression in patients with unresectable HCC receiving intra-arterial chemotherapy with cisplatin and mitomycin-C wk 7 of each cycle [clinicaltrials_resource:2f696e908d15932401d049fc0e52ebfc]
CDDP 60mg/m2 + Mitomycin-C 12mg/m2
Bio2RDF identifier
2f696e908d15932401d049fc0e52ebfc
Bio2RDF namespace
clinicaltrials_resource
Bio2RDF uri
http://bio2rdf.org/clinicaltrials_resource:2f696e908d15932401d049fc0e52ebfc
measure [clinicaltrials_vocabulary:measure]
To assess time to progression ...... with cisplatin and mitomycin-C
time frame [clinicaltrials_vocabulary:time-frame]
wk 7 of each cycle
description
CDDP 60mg/m2 + Mitomycin-C 12mg/m2
identifier
clinicaltrials_resource:2f696e908d15932401d049fc0e52ebfc
title
To assess time to progression ...... mitomycin-C wk 7 of each cycle
@en
type
label
To assess time to progression ...... 96e908d15932401d049fc0e52ebfc]
@en