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Clinical Trials/NCT01430052
NCT01430052
Completed
Phase 2

Randomized Phase II Study Comparing Gemcitabine/S-1 Combination Chemoradiotherapy With Gemcitabine/S-1 Combination Chemotherapy for Unresectable Locally Advanced Pancreatic Cancer.

Osaka Medical Center for Cancer and Cardiovascular Diseases1 site in 1 country110 target enrollmentApril 2009

Overview

Phase
Phase 2
Intervention
gemcitabine, S-1, radiotherapy
Conditions
Pancreatic Cancer
Sponsor
Osaka Medical Center for Cancer and Cardiovascular Diseases
Enrollment
110
Locations
1
Primary Endpoint
Two year survival rate
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the clinical effectiveness of Gemcitabine/S-1 combination chemoradiotherapy with Gemcitabine /S-1 combination chemotherapy for unresectable locally advanced pancreatic cancer.

Detailed Description

When cancer develops outside of the pancreas from within the anatomical placement of the pancreas itself, it becomes difficult to excise in most cases. Generally, most pancreatic cancers are already unresectable at the time of diagnosis when we have recognized infiltration of over 1/2 the circumference of major arteries such as the celiac artery and super mesenteric artery in particular. In comparison with advanced pancreatic cancer with distant metastases, it is not easy to treat unresectable locally advanced pancreatic cancer, even when performing standard gemcitabine monotherapy. In the case of unresectable locally advanced pancreatic cancers without distant metastases, we are left with the choice of whether or not to perform radiation therapy. This decision remains unsolved worldwide, despite the continuing efforts of researchers to bring an end to the clinical doubt. We will report our results as well as the problems of combining treatments with chemoradiotherapy, using the novel anticancer agent gemcitabine as well as/or S-1, not 5FU, predominantly from our own clinical trials on this occasion.

Registry
clinicaltrials.gov
Start Date
April 2009
End Date
September 2015
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Osaka Medical Center for Cancer and Cardiovascular Diseases
Responsible Party
Principal Investigator
Principal Investigator

Tatsuya Ioka

Assistant director

Osaka Medical Center for Cancer and Cardiovascular Diseases

Eligibility Criteria

Inclusion Criteria

  • Histologically or cytologically confirmed adenocarcinoma, adenocarcinoma squamous carcinoma of pancreatic cancer.
  • Patients who confirmed unresectable locally advanced pancreatic cancer with the criteria below.
  • Involving over 1/2 circumference of major artery (SMA/CA). (Under 1/2 that was borderline lesion.)
  • Involving over the merging section of portal-SMV.
  • No distal metastasis with diagnostic imaging.
  • Confirmed by CT image performed with in four weeks before registration.
  • Performance Status:0-1(ECOG)
  • Patients of age =\>20 and 80\>
  • sufficient organ functions
  • neutrophils\>=1,500/mm3

Exclusion Criteria

  • Lung fibrosis or intestinal pneumonia, and anamnesis or imaging findings.
  • Watery diarrhea
  • Severe infection
  • Severe complication (heart failure, renal failure, hepatic insufficiency,hemorrhagic peptic ulcer, intestines paralysis,ileus or uncontrolled diabetes etc)
  • Massive pleural or abdominal effusion.
  • Metastasis to central nervous system.
  • Active synchronous or metachronous malignancy other than carcinoma in situ.
  • Regular use of flucytosine, fenitoin or warfarin
  • Pregnant or lactation women, or women with known or suspected pregnancy and men who want let to pregnancy
  • Severe mental illness

Arms & Interventions

Gemcitabine, S-1, radiotherapy

Gemcitabine 600mg/m2 on Day 1 and 8, every 3 weeks. S-1 60-100mg/day on Day 1 to 14, every 3 weeks with radiotherapy 50.4Gy in 28 fractions

Intervention: gemcitabine, S-1, radiotherapy

Outcomes

Primary Outcomes

Two year survival rate

Time Frame: 2 years

Secondary Outcomes

  • Progression free survival(PFS)(4 years)
  • Adverse events(4 years)
  • Response rate(4 years)
  • Overall Survival (OS)(4 years)

Study Sites (1)

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