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5-FU local injection for the treatment of advanced gastric cancer

Not Applicable
Recruiting
Conditions
Diseases of the digestive system
Registration Number
KCT0008395
Lead Sponsor
Kangbuk Samsung Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
35
Inclusion Criteria

Patients aged 18 years or older with histologically confirmed adenocarcinoma and diagnosed with advanced gastric cancer that is not amenable to radical resection at the time of diagnosis who meet the following conditions are eligible.
Patients who have failed standard treatment or for whom standard treatment is not feasible,
Patients with measurable lesions in the stomach on endoscopy,
Patients with a predicted survival time of 3 months or more.

Exclusion Criteria

?Patients with a history of cancer other than gastric cancer
?Patients who do not consent to this treatment
?Nursing mothers other than pregnant women or women of childbearing potential who are planning to become pregnant
?Patients receiving Tegapur-Gimeracil-Oterasil potassium combination and patients who have stopped taking it within 7 days.
?Patients receiving sorbudine
?Patients with a history of severe hypersensitivity to 5-FU
?Patients with bone marrow depression after treatment with other antineoplastic agents, radiation therapy, or extreme frailty
?Patients with non-malignant tumor disease

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Objective response rate (ORR; objective response rate): Percentage of patients with an objective response, such as a reduction in tumor size, relative to the total number of patients.
Secondary Outcome Measures
NameTimeMethod
Changes in tumor size and area on endoscopy
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