This study is to assess the response rate, toxicity, time-to-event efficacy, and potential markers of pemetrexed in patients with liver cancer.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
41
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
Denver, Colorado, United States
Antitumor activity as measured by Response Evaluation Criteria in Solid Tumors
Toxicity measured by CTCAE grading
Duration of response: First complete or partial response until progressive disease (PD) or death of any cause
Duration of stable disease: Enrollment to PD or death of any cause
Time to treatment failure: Enroll. to PD, death of any cause, early discontinuation of treatment for any reason other than adequate response or start of new therapy
Progression-free survival: Enroll. to PD or death of any cause
Overall survival: Enroll. to death of any cause
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