Irinotecan, as one new agent used in advanced esophageal carcinoma, has been shown to be effective and safe in western studies. Different with westerns, squamous carcinoma is the main pathological type in china patients. The investigators then initiated a prospective phase II clinical trial with irinotecan/cisplatin as the 1st line treatment in advanced esophageal carcinoma to observe the efficacy and safety of the combination.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
60
irinotecan 130mg/m2 d1 cisplatin 30mg/m2, d1,d2 every 3 weeks
Zhang Xiaodong
Beijing, Beijing Municipality, China
RECRUITINGoverall survival
Time frame: 2 year
PFS
Time frame: 1year
response rate
Time frame: 1.5 months
adverse events
Time frame: 2 year
polymorphism of UGT1A
Time frame: 2 year
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