UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000000573
Receipt number R000000698
Scientific Title Phase I/II study of arterial infusion of 5-fluorouracil combined with systemic gemcitabine for unresectable pancreatic cancer
Date of disclosure of the study information 2007/01/16
Last modified on 2010/07/13 22:58:08

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Basic information

Public title

Phase I/II study of arterial infusion of 5-fluorouracil combined with systemic gemcitabine for unresectable pancreatic cancer

Acronym

HAI-5-FU combined with GEM for unresectable pancreatic cancer

Scientific Title

Phase I/II study of arterial infusion of 5-fluorouracil combined with systemic gemcitabine for unresectable pancreatic cancer

Scientific Title:Acronym

HAI-5-FU combined with GEM for unresectable pancreatic cancer

Region

Japan


Condition

Condition

Unresectable pancreatic cancer

Classification by specialty

Hepato-biliary-pancreatic medicine Hematology and clinical oncology Hepato-biliary-pancreatic surgery
Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To determine the dose limiting toxicity (DLT) and the recommended dose (RD) of arterial infusion of 5-FU combined with GEM in patients with unresectable pancreatic cancer, and to evaluate safety and efficacy with this therapy.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Phase I,II


Assessment

Primary outcomes

Adverse reaction

Key secondary outcomes

Response rate, progression-free survival and over all surval


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Medicine Maneuver

Interventions/Control_1

Patients receive arterial infusion of 5-FU via an indwelling catheter and port system and systemic GEM at day 1,8, and 15. Treatment repeats every 4 weeks for 5 courses in the absence of disease progression or unacceptable toxicity.

Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit

75 years-old >=

Gender

Male and Female

Key inclusion criteria

1)confirmention of pathologicaly proven invasive pancreatic ductal cancer (adenocarcinoma)
2)Unresectable because of locally advanced pancreatic lesion and/or liver metastases
3)Measurable lesion in the live and/or pancreas according to RECIST
4)malignant lesion in other organ
5)no prior treatment except for surgery
6)PS=0-1(Eastern Cooperative Oncology Group (ECOG) performance )
7)adequate hepatic, renal, bone marrow function
Expected survival more than 8 weeks.
WBC count>=3,000/L
ANC >=1500/L
platelet count>=100,000/L
Hb >=9.0mg/dl
T-bil <=3.0mg/dl
AST/ALP <=5times the upper nomal limits
Cre <=1.5mg/dl
8)written informed concent


Key exclusion criteria

1)distant metastaes except of liver and node
2)adequate drug distribution via celiac arterial infusion with alteration of pancreatic blood flow will not be achieved
3)Interstitial pneumonia in chest X-ray
4)active gastro-duodenal ulcer
5)Allergic reaction to iodine contrast material.
6)Infectious disease with fever over 38 degree Celcius or antibiotics required.
7)Pregnant or nursing.
8)Severe drug allergic reaction
9)The other severe complicated disease




Target sample size

24


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Toshihiro Tanaka

Organization

Nara Medical University

Division name

Dept of radiology

Zip code


Address

840 Shijocho Kashiharashi city , Japan

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name Toshihiro Tanaka

Organization

Nara Medical University

Division name

Dept of radiology

Zip code


Address

840 Shijocho Kashiharashi city , Japan

TEL

0744-29-8900

Homepage URL


Email

rad@naramed-u.ac.jp


Sponsor or person

Institute

Nara Medical University

Institute

Department

Personal name



Funding Source

Organization

non

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2007 Year 01 Month 16 Day


Related information

URL releasing protocol


Publication of results

Partially published


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2006 Year 09 Month 01 Day

Date of IRB


Anticipated trial start date

2006 Year 10 Month 01 Day

Last follow-up date

2010 Year 07 Month 01 Day

Date of closure to data entry

2010 Year 07 Month 01 Day

Date trial data considered complete

2010 Year 07 Month 01 Day

Date analysis concluded

2010 Year 07 Month 01 Day


Other

Other related information



Management information

Registered date

2007 Year 01 Month 13 Day

Last modified on

2010 Year 07 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000000698


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name