The main purpose of this study is to determine the effects of treatment with carboplatin, docetaxel and capecitabine in patients with incurable cancer of the esophagus or stomach.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
98
Finsen Center, Rigshospitalet
Copenhagen, Denmark
The proportion of participants alive one year after randomisation
Time frame: Three and a half years
Time to progression or death due to any cause
Time frame: Three and a half years
Number of participants with grade 3 and 4 toxicities caused by treatments
Time frame: Day 1 of every cycle and 30 days after completion of treatment
Time until death due to any cause
Time frame: Three and a half years
Changes in quality-of-life
Time frame: Three and a half years
The proportion of participants who have carboplatin, docetaxel and capecitabine re-induced
Time frame: Five years
Registration of further lines of therapy
Time frame: Five years
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