Unique ID issued by UMIN | UMIN000002649 |
---|---|
Receipt number | R000003226 |
Scientific Title | Phase I/II study of preoperative chemoradiotherapy with Gemcitabine and S-1 for resectable pancreatic cancer |
Date of disclosure of the study information | 2009/10/19 |
Last modified on | 2024/05/10 14:40:16 |
Phase I/II study of preoperative chemoradiotherapy with Gemcitabine and S-1 for resectable pancreatic cancer
Phase I/II study of preoperative chemoradiotherapy with Gemcitabine and S-1 for resectable pancreatic cancer
Phase I/II study of preoperative chemoradiotherapy with Gemcitabine and S-1 for resectable pancreatic cancer
Phase I/II study of preoperative chemoradiotherapy with Gemcitabine and S-1 for resectable pancreatic cancer
Japan |
resectable pancreatic cancer
Hepato-biliary-pancreatic surgery |
Malignancy
NO
To evaluate the safety and feasibility, to determine recommended dose (RD) and to evaluate the efficacy of preoperative chemoradiotherapy with Gemcitabine and S-1 in patients with resectable pancreatic cancer
Safety,Efficacy
Phase 1: Dose limiting toxicity, maximum tolerated dose, recommended dose
Phase 2: Pathological effect
Response rate, Safety, Curative resection rate, Feasibility, Local recurrence rate, Relapse free survival (RFS), Overall survival (OS)
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Medicine |
preoperative chemoradiotherapy with Gemcitabine and S-1
20 | years-old | <= |
80 | years-old | >= |
Male and Female
(1) Histologically proven pancreatic adenocarcinoma
(2) Age between 20 and 80 years
(3) ECOG performance status of 0 or 1
(4) Surgically resectable
(5) Life Expectancy must be >=6 months
(6) Adequate hematologic, hepatic, renal and respiratory function
(7) Interval of at least 4 weeks between prior treatment and start of present study
(8) Written informed consent
(1) Unresectable pancreatic cancer
(2) Presence or past history of Interstitial pneumonia or pulmonary fibrosis or possible
(3) Watery diarrhea
(4) Active infections (excluding viral hepatitis)
(5) Severe cardiac disorder, renal disorder, liver disorder, ulcer with bleeding, intestinal tract paralysis, uncontrollable diabetes mellitus
(6) Presence of pleural effusion or ascites requiring drainage
(7) Presence of metastasis in central nervous system
(8) Active double cancer except carcinoma in situ or intramucosal cancer (synchronous double cancer or asynchronous double cancer with disease-free duration to be within 3 years)
(9) Treatment with phenytoin, potassium warfarin or flucytosine
(10) Pregnant females or nursing mothers who can not stop lactation. Patients or partners, who don't attempt to doing contraception during the study period.
(11) Severe mental disorder
(12) Severe drug hypersensitivity
(13) As determined by the principal investigator or the sub-investigator the subject is not adequate to participate in the trial.
55
1st name | Hidetoshi |
Middle name | |
Last name | Eguchi |
Osaka University
Gastroenterological Surgery
565-0871
2-2 Yamadaoka, Suita, Osaka, Japan
06-6879-3251
heguchi@gesurg.med.osaka-u.ac.jp
1st name | Hidetoshi |
Middle name | |
Last name | Eguchi |
Osaka University
Gastroenterological Surgery
565-0871
2-2 Yamadaoka, Suita, Osaka, Japan
06-6879-3251
heguchi@gesurg.med.osaka-u.ac.jp
Multicenter Clinical Study Group of Osaka
None (Self-funding)
Self funding
Osaka University Clinical Research Review Committee
2-2 Yamadaoka Suita, Osaka 565-0871, Japan
06-6210-8296
handai-nintei@hp-crc.med.osaka-u.ac.jp
NO
2009 | Year | 10 | Month | 19 | Day |
Unpublished
63
Completed
2009 | Year | 10 | Month | 15 | Day |
2009 | Year | 10 | Month | 15 | Day |
2009 | Year | 10 | Month | 01 | Day |
2020 | Year | 08 | Month | 31 | Day |
2020 | Year | 08 | Month | 31 | Day |
2020 | Year | 08 | Month | 31 | Day |
2021 | Year | 03 | Month | 31 | Day |
2009 | Year | 10 | Month | 19 | Day |
2024 | Year | 05 | Month | 10 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000003226