Neoplasm Metastasis Clinical Trial
The primary objective of the study is to Evaluate the response rate of Gemcitabine with TS-1 in Korean patient with advanced but inoperable, metastatic or recurrent pancreatic cancer who is not receiving anti cancer therapy.
To date, curative treatment of pancreatic cancer is surgery.But patients with operable
indication are rare, most of patients present with locally advanced or general advanced
stage at diagnosis. Thus the majority of patients need chemotherapy.But efficacy outcomes
have not seemed to increase overall survival comparing with none treated control group.In
Korea the incidence of pancreatic cancer increases steadily. Prognosis is poor. So now the
effective treatment is necessary.There are no phase 2 trialsabout combining gemcitabine and
TS-1 against advanced pancreatic cancer.according to phase 1 trial of advanced pancreatic
cancer (nakamura et al)toxicities more than 3 grade are neutropenia, anemia,
thrombocytopenia, anorexia, etc that can be treated.Phase 1 trial is not study to evaluate
the response rate. But among 21 patients who can be evaluated the response rate, 10 patients
have Partial response or Complete response.This combination therapy seemed to havetolerable
toxicity and remarkable therapeutic effect for locally advanced or metastatic pancreatic
cancer.So therapy combining gemcitabine with TS-1 is expected synergic and additional
effect.
This trial is phase 2, open-label, multi-center, single arm study The total sample size will
be 38 patients. Patient will be administered chemotherapy until disease progression.
Gemcitabine will be administered at a dose of 1000 mg/m2 every 3weeks (on day 1 of each
cycle) TS-1 will be administered 80 mg/m2 orally twice daily for 14 days every 3 weeks.
;
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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