UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000013809
Receipt number R000016112
Scientific Title The pilot study of neoadjuvant chemotherapy of FIRINOX for patients with borderline resectable pancreatic cancer
Date of disclosure of the study information 2014/04/25
Last modified on 2016/04/25 20:41:04

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Basic information

Public title

The pilot study of neoadjuvant chemotherapy of FIRINOX for patients with borderline resectable pancreatic cancer

Acronym

FIRINOX

Scientific Title

The pilot study of neoadjuvant chemotherapy of FIRINOX for patients with borderline resectable pancreatic cancer

Scientific Title:Acronym

FIRINOX

Region

Japan


Condition

Condition

Invasive ductal carcinoma

Classification by specialty

Hepato-biliary-pancreatic medicine Hepato-biliary-pancreatic surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the safety, efficacy and optimal treatment schedule of FIRINOX therapy as neoadjuvant chemotherapy for Borderline resectable pancreatic cancer.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

(1)Adverse event

Key secondary outcomes

(1)R0 resection rate
(2)Resection rate
(3)Optimal number of courses administration of neoadjuvant chemotherapy
(4)Optimal duration of surgery to perform from neoadjuvant chemotherapy


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

Interventions/Control_1

neoadjuvant chemotherapy
4 courses of FIRINOX
L-OHP 85mg/m2 administration
CPT-11 150mg/m2
administration
5-FU 2,400mg/m2 46hours infusion

neoadjuvant chemotherapy
8 courses of FIRINOX
L-OHP 85mg/m2 administration
CPT-11 150mg/m2
administration
5-FU 2,400mg/m2 46hours infusion

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

80 years-old >

Gender

Male and Female

Key inclusion criteria

(1)Pathologically proven invasive pancreatic ductal carcinoma
(2)Cases that meet the definition of borderline resectable pancreatic cancer 1) or 2)
1) Definition of a borderline resectable pancreatic cancer is filledin NCCN guideline version 1.2014 pancreatic adenocarcinoma
2) Patients indicated distal pancreatectomy with en bloc celiac axis resection
(3)PS (ECOG) 0-1
(4)>=20 years old and < 75 years old
(5)First line treatment
(6)The following criteria must be satisfied in laboratory tests within 14 days of registration
White blood cell count <=12,000/mm3
Neutrophil count >=1,500/mm3
Platelet count >=100,000mm3
Total bilirubin <2.0mg/dL
Serum Creatinine <=upper limits of normal(ULN)
AST,ALT<= 2.5xULN
Albumin>=3.0g/dL
Hemoglobin>=9.0g/dL
(7)Written informed consent to participate in this study
(8)Pancreatic head carcinoma without biliary drainage

Key exclusion criteria

(1)Severe drug hypersensitivity
(2)Multiple primary cancers within 5 years
(3)Severe infection
(4)With grade 2 or more severe peripheral neuropathy
(5)With intestinal paralysys, ileus
(6)Interstitial pneumonia or pulmonary
(7)With uncontrollable pleural effusion or ascites
(8)Receiving atazanavir sulfate
(9)With uncontrollable diabetes
(10)With uncontrollable heart failure, angina, hypertension, arrhythmia
(11)With severe psychological symptoms
(12)With watery diarrhea
(13)Pregnant or lactating women, or
women with known or suspected pregnancy
(14)Inappropriate patients for entry on this study in the judgment of the investigator
(15)With UGT1A1*28 and/or
UGT1A1*6 polymorphisms

Target sample size

10


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiroki Yamaue

Organization

Wakayama Medical University

Division name

Second department of surgery

Zip code


Address

811-1 Kimiidera, Wakayama

TEL

073-447-2300

Email

yamaue-h@wakayama-med.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Ken-ichi Okada

Organization

Wakayama Medical University

Division name

Second Department of Surgery

Zip code


Address

811-1 Kimiidera, Wakayama

TEL

073-441-0613

Homepage URL


Email

okada@wakayama-med.ac.jp


Sponsor or person

Institute

Wakayama Medical University

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Other

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

神戸大学大学(兵庫県)、関西医科大学(大阪府)、奈良県立医科大学(奈良県)、大阪大学(大阪府)、広島大学(広島県)、名古屋大学(愛知県)、大阪府立成人病センター(大阪府)、大阪市立大学(大阪府)、和歌山県立医科大学(和歌山県)


Other administrative information

Date of disclosure of the study information

2014 Year 04 Month 25 Day


Related information

URL releasing protocol


Publication of results

Unpublished


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

2014 Year 03 Month 08 Day

Date of IRB


Anticipated trial start date

2014 Year 04 Month 28 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2014 Year 04 Month 25 Day

Last modified on

2016 Year 04 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000016112


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name